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    <title>Recent ucr_som_biomed_oapolicydeposits items</title>
    <link>https://escholarship.org/uc/ucr_som_biomed_oapolicydeposits/rss</link>
    <description>Recent eScholarship items from Biomedical Sciences Open Access Policy Deposits</description>
    <pubDate>Sat, 1 Aug 2026 16:24:29 +0000</pubDate>
    <item>
      <title>TGFβ signaling is required during human and chick Neural Crest formation</title>
      <link>https://escholarship.org/uc/item/8vx2b572</link>
      <description>Neural crest (NC) cells are multipotent cells unique to vertebrates that arise early in development, at the edge of the neural plate, and subsequently undergo an epithelial to mesenchymal transition, migrate throughout the body, and differentiate into many different derivatives, contributing to the formation of many organs and systems. NC induction research from multiple modeling organisms has identified critical roles for a few signaling pathways, including Wnt, BMP, FGF, Notch/ Delta, Indian Hedgehog, and Endothelin signaling (Prasad et al., 2019). Given the limitations of human embryo studies, pluripotent stem cell models of human NC formation have provided a resourceful alternative (Lee et al., 2007). Intriguingly, while TGFβ inhibition had not been identified as a signaling requirement for NC formation in any in vivo model organism, several pluripotent stem cell (PSC) models of human NC induction rely on TGFβ inhibition (Chambers et al., 2009). To address this issue, we evaluate...</description>
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      <pubDate>Sun, 7 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Gomez, Gustavo A</name>
      </author>
      <author>
        <name>Parmar, Bhaval</name>
      </author>
      <author>
        <name>Wong, Man</name>
      </author>
      <author>
        <name>Hernandez, Jacqueline C</name>
      </author>
      <author>
        <name>Guimarães-Andrade, Iris Paula</name>
      </author>
      <author>
        <name>Garcia-Castro, Martin I</name>
        <uri>https://orcid.org/0000-0001-5128-0004</uri>
      </author>
    </item>
    <item>
      <title>Decoding the origins of cellular self-organization for engineered biology</title>
      <link>https://escholarship.org/uc/item/8xg946qf</link>
      <description>Decoding the origins of cellular self-organization for engineered biology</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8xg946qf</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Chen, Qi</name>
        <uri>https://orcid.org/0000-0001-6353-9589</uri>
      </author>
      <author>
        <name>Zernicka-Goetz, Magdalena</name>
        <uri>https://orcid.org/0000-0002-7004-2471</uri>
      </author>
    </item>
    <item>
      <title>Proposed Key Characteristics of Neurotoxic Chemicals</title>
      <link>https://escholarship.org/uc/item/7wp0129j</link>
      <description>A critical component of evaluating whether a chemical can cause human neurotoxicity is hazard identification, which typically involves a comprehensive literature search to identify and synthesize epidemiological, animal, and mechanistic data for the chemical of interest. The key characteristics (KCs) concept has proven to be a useful tool for searching, organizing, and evaluating mechanistic data for hazard identification. KCs are the established chemical and biological properties of known human neurotoxic agents based on understanding of their mechanisms of neurotoxicity. KCs were originally developed for carcinogens but have now also been published for endocrine- and metabolism-disruptors and various organ-selective toxic chemicals. To identify KCs associated with neurotoxic chemicals, an expert committee was convened to consider current mechanistic understanding of chemicals known to be neurotoxic in humans with the goal of identifying established molecular and cellular actions...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7wp0129j</guid>
      <pubDate>Wed, 11 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Lein, Pamela J</name>
        <uri>https://orcid.org/0000-0001-7665-7584</uri>
      </author>
      <author>
        <name>Bowman, Aaron B</name>
      </author>
      <author>
        <name>Cao, Zhengyu</name>
      </author>
      <author>
        <name>Carson, Monica</name>
      </author>
      <author>
        <name>Eskenazi, Brenda</name>
        <uri>https://orcid.org/0000-0001-7609-6852</uri>
      </author>
      <author>
        <name>Fritsche, Ellen</name>
      </author>
      <author>
        <name>Harry, G Jean</name>
      </author>
      <author>
        <name>Hartung, Thomas</name>
      </author>
      <author>
        <name>Pessah, Isaac N</name>
      </author>
      <author>
        <name>Slikker, William</name>
      </author>
      <author>
        <name>Zeise, Lauren</name>
      </author>
      <author>
        <name>Smith, Martyn T</name>
      </author>
    </item>
    <item>
      <title>A cholesterol-responsive hepatic tRNA-derived small RNA regulates cholesterol homeostasis and atherosclerosis development</title>
      <link>https://escholarship.org/uc/item/9rx4r1cb</link>
      <description>Transfer RNA-derived small RNAs (tsRNAs) have emerged as crucial players in diverse biological processes. Yet, their involvement in lipid metabolism and cardiovascular disease remains elusive. Using an advanced PANDORA-seq method, we identify tsRNA-Glu-CTC as the most abundant tsRNA in mouse liver. Intriguingly, tsRNA-Glu-CTC is cholesterol responsive. Overexpression of tsRNA-Glu-CTC elicits hypercholesterolemia and hepatic steatosis, whereas its knockdown protects against diet-induced hypercholesterolemia and atherosclerosis in mice. Mechanistically, tsRNA-Glu-CTC regulates key hepatic lipogenic genes including Srebp2, a master regulator of lipid metabolism. tsRNA-Glu-CTC interacts with SREBP2 to regulate its own transcription through an E-box motif. We further identify site-specific RNA modifications of endogenous tsRNA-Glu-CTC by a mass spectrometry-based MLC-seq and demonstrate the modified tsRNA-Glu-CTC as a more potent regulator of cholesterol homeostasis compared to its...</description>
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      <pubDate>Mon, 22 Dec 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Li, Xiuchun</name>
      </author>
      <author>
        <name>Hernandez, Rebecca</name>
        <uri>https://orcid.org/0000-0002-8031-2949</uri>
      </author>
      <author>
        <name>Zhang, Xudong</name>
      </author>
      <author>
        <name>Tang, Sijie</name>
      </author>
      <author>
        <name>Yuan, Xiaohong</name>
      </author>
      <author>
        <name>Wu, Jing</name>
      </author>
      <author>
        <name>Pham, Kathy</name>
      </author>
      <author>
        <name>Rawal, Hukam C</name>
      </author>
      <author>
        <name>Heinrich, Erica C</name>
      </author>
      <author>
        <name>Zhang, Shenglong</name>
      </author>
      <author>
        <name>Chen, Qi</name>
        <uri>https://orcid.org/0000-0001-6353-9589</uri>
      </author>
      <author>
        <name>Zhou, Tong</name>
      </author>
      <author>
        <name>Zhou, Changcheng</name>
      </author>
    </item>
    <item>
      <title>Durable humoral immunity and long-term protection induced by a Crimean-Congo hemorrhagic fever virus replicon particle vaccine in mice</title>
      <link>https://escholarship.org/uc/item/7pr3n5jb</link>
      <description>A Crimean-Congo hemorrhagic fever virus replicon particle vaccine was evaluated for long-term immunity and efficacy in mice. IgG responses persisted up to 18 months, with similar titers across dosing strategies through 12 months. Protective efficacy reached ≥75% at 6 months (prime-only) and up to 12 months (prime-boost). Booster dosing enhanced antibody avidity, effector function, and improved long-term protection. These findings support durable immunity from single or boosted vaccination.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7pr3n5jb</guid>
      <pubDate>Mon, 8 Dec 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Sorvillo, Teresa E</name>
      </author>
      <author>
        <name>Karaaslan, Elif</name>
      </author>
      <author>
        <name>Davies, Katherine A</name>
      </author>
      <author>
        <name>Welch, Stephen R</name>
      </author>
      <author>
        <name>Scholte, Florine EM</name>
      </author>
      <author>
        <name>Coleman-McCray, JoAnn D</name>
      </author>
      <author>
        <name>Aida-Ficken, Virginia</name>
      </author>
      <author>
        <name>Pegan, Scott D</name>
        <uri>https://orcid.org/0000-0002-2958-5319</uri>
      </author>
      <author>
        <name>Bergeron, Éric</name>
      </author>
      <author>
        <name>Montgomery, Joel M</name>
      </author>
      <author>
        <name>Spiropoulou, Christina F</name>
      </author>
      <author>
        <name>Spengler, Jessica R</name>
      </author>
    </item>
    <item>
      <title>PTBP1 depletion in mature astrocytes reveals distinct splicing alterations without neuronal features</title>
      <link>https://escholarship.org/uc/item/6fg322fk</link>
      <description>Astrocyte-to-neuron reprogramming via depletion of PTBP1, a potent repressor of neuronal splicing, has been proposed as a therapeutic strategy, but its efficacy remains debated. While some reported successful conversion, others disputed this, citing a lack of neuronal gene expression as evidence of failed reprogramming. This interpretation was further challenged, attributed to incomplete PTBP1 inactivation, fueling ongoing controversy. Mechanistic understanding of the conversion, or the lack thereof, requires investigating, in conjunction with lineage tracing, the effect of &lt;i&gt;Ptbp1&lt;/i&gt; loss of function in mature astrocytes on RNA splicing, which has not yet been examined. Here, we genetically ablated PTBP1 in adult Aldh1l1-Cre/ERT2 Ai14 mice to determine whether lineage-traced &lt;i&gt;Ptbp1&lt;/i&gt; knockout astrocytes exhibited RNA splicing alterations congruent with neuronal differentiation. We found no widespread induction of neurons, despite a minuscule fraction of knockout cells showing...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6fg322fk</guid>
      <pubDate>Tue, 25 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Zhang, Min</name>
      </author>
      <author>
        <name>Kubota, Naoto</name>
        <uri>https://orcid.org/0000-0003-0612-2300</uri>
      </author>
      <author>
        <name>Nikom, David</name>
      </author>
      <author>
        <name>Arient, Ayden</name>
      </author>
      <author>
        <name>Zheng, Sika</name>
      </author>
    </item>
    <item>
      <title>A conserved long-range RNA interaction in SARS-CoV-2 recruits ADAR1 to enhance virus proliferation</title>
      <link>https://escholarship.org/uc/item/3nf448x7</link>
      <description>Long-range RNA-RNA pairing impacts the genome structure and function of SARS-CoV-2 variants. To understand the structure and function relationships of different SARS-CoV-2 variants that have emerged during the COVID-19 pandemic, we perform high-throughput structure probing and modelling of the genomic structures of the wildtype (WT), Alpha, Beta, Delta and Omicron variants of SARS-CoV-2. We observe that genomes of SARS-CoV-2 variants are generally structurally conserved, and that single-nucleotide variations and interactions with RNA binding proteins can impact RNA structures across the viruses. Importantly, using proximity ligation sequencing, we identify many conserved ultra-long-range RNA-RNA interactions, including one that spans more than 17 kb in both the WT virus and the Omicron variant. We show that mutations that disrupt this 17 kb long-range interaction reduce viral fitness at later stages of its infection cycle, while compensatory mutations partially restore virus fitness....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3nf448x7</guid>
      <pubDate>Thu, 23 Oct 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Yang, Siwy Ling</name>
      </author>
      <author>
        <name>DeFalco, Louis</name>
      </author>
      <author>
        <name>Wang, Sainan</name>
      </author>
      <author>
        <name>Wong, Yi Hao</name>
      </author>
      <author>
        <name>Han, Jian</name>
      </author>
      <author>
        <name>Mok, Chee Keng</name>
      </author>
      <author>
        <name>Tan, Kiat Yee</name>
      </author>
      <author>
        <name>Lim, Su Ying</name>
      </author>
      <author>
        <name>Zhao, Zhiya</name>
      </author>
      <author>
        <name>Zhang, Yu</name>
      </author>
      <author>
        <name>Lim, Jovi Jian An</name>
      </author>
      <author>
        <name>Xiang, Joy S</name>
      </author>
      <author>
        <name>Sobota, Radoslaw</name>
      </author>
      <author>
        <name>Wang, Lin-Fa</name>
      </author>
      <author>
        <name>Chu, Justin Jang Hann</name>
      </author>
      <author>
        <name>Merits, Andres</name>
      </author>
      <author>
        <name>Huber, Roland G</name>
      </author>
      <author>
        <name>Wan, Yue</name>
      </author>
    </item>
    <item>
      <title>Rapid, sensitive, and species-independent detection of Crimean Congo hemorrhagic fever virus nucleoprotein and GP38 antibodies</title>
      <link>https://escholarship.org/uc/item/5792d8d1</link>
      <description>BACKGROUND: Crimean-Congo hemorrhagic fever virus (CCHFV), a zoonotic agent in the Nairoviridae family (genus Orthonairovirus), is a high-priority pathogen. CCHFV infection causes Crimean-Congo hemorrhagic fever (CCHF), a human disease with case fatality rates of up to 40%. Serological surveillance of CCHFV in animals and humans is crucial for ecological studies and public health.
METHODS: We developed CCHFV mix-and-read assays utilizing split-NanoLuc technology (NanoBiT) to detect anti-CCHFV antibodies against the nucleoprotein (NP) stalk region and the GP38 glycoprotein. These species- and isotype-agnostic assays provide results in ∼30 min. Using serum samples from RT-PCR-confirmed CCHF cases collected during and after hospitalization, we investigated anti-NP and anti-GP38 antibody development. The performance of the mix-and-read assays was compared to the NP-based IDScreen® CCHF commercial assay using human sera, and cross-reactivity potential was evaluated using a diverse...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5792d8d1</guid>
      <pubDate>Thu, 14 Aug 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Karaaslan, Elif</name>
      </author>
      <author>
        <name>Chiang, Cheng-Feng</name>
      </author>
      <author>
        <name>Kurutaş, Gülter Öncü</name>
      </author>
      <author>
        <name>Barkay, Orçun</name>
      </author>
      <author>
        <name>Güler, Nesibe Selma Çetin</name>
      </author>
      <author>
        <name>Kalkan, Merve Yazıcı</name>
      </author>
      <author>
        <name>Parlayan, Hanife Nur Karakoç</name>
      </author>
      <author>
        <name>Akdoğan, Özlem</name>
      </author>
      <author>
        <name>Çelikbaş, Aysel Kocagül</name>
      </author>
      <author>
        <name>Aksoy, Firdevs</name>
      </author>
      <author>
        <name>Binay, Umut Devrim</name>
      </author>
      <author>
        <name>Baykam, Nurcan</name>
      </author>
      <author>
        <name>Yılmaz, Gürdal</name>
      </author>
      <author>
        <name>Sajadi, Mohammad M</name>
      </author>
      <author>
        <name>Pegan, Scott D</name>
        <uri>https://orcid.org/0000-0002-2958-5319</uri>
      </author>
      <author>
        <name>Klena, John D</name>
      </author>
      <author>
        <name>Montgomery, Joel M</name>
      </author>
      <author>
        <name>Karakeçili, Faruk</name>
      </author>
      <author>
        <name>Kalkan, Ahmet</name>
      </author>
      <author>
        <name>Doymaz, Mehmet Ziya</name>
      </author>
      <author>
        <name>Spiropoulou, Christina F</name>
      </author>
      <author>
        <name>Bergeron, Éric</name>
      </author>
    </item>
    <item>
      <title>Neuroendocrinology and the Genetics of Obesity</title>
      <link>https://escholarship.org/uc/item/9fs9w67h</link>
      <description>The increase in the incidence of obesity has coincided with changes in lifestyle, diet, and environment. Comorbidities associated with obesity include cardiovascular disease, diabetes, musculoskeletal disorders, stroke, and thromboembolism, affecting public health. The effect of increased weight has recently become even more obvious, since obesity has been significantly associated with increased severity and higher mortality among COVID-19 patients. The need to decrease rates of obesity prompted a surge in the use of glucagon-like peptide-1 agonist medications. Twin studies, however, determined that increased weight has a large genetic component, estimating the heritability of obesity to be 45% to 70%. Surprisingly, obesity due to known single gene mutation comprises only 5% to 10% of individuals, who mostly exhibit early-onset severe obesity. Genome-wide linkage studies and association studies identified more than 250 genes associated with obesity, but each of these has a relatively...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9fs9w67h</guid>
      <pubDate>Mon, 4 Aug 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Ruggiero-Ruff, Rebecca E</name>
      </author>
      <author>
        <name>Coss, Djurdjica</name>
        <uri>https://orcid.org/0000-0003-0692-1612</uri>
      </author>
    </item>
    <item>
      <title>Identification of reference genes for quantitative PCR analyses in developing mouse gonads</title>
      <link>https://escholarship.org/uc/item/42j7v246</link>
      <description>Stable reference genes are important for gene expression analyses such as quantitative PCR. The stability of 15 candidate reference genes that can be used to developing mouse gonads was thoroughly verified using combinations of multiple algorithms. The expression of these genes fluctuated greatly depending on the analysis period and/or gender. Peptidylprolyl isomerase A (Ppia) and polymerase (RNA) II (DNA directed) polypeptide A (Polr2a) were the reference genes that were used stably for a wide analysis period in developing mouse gonads. Furthermore, the stable reference genes corresponding to the analysis period and/or gender were ranked. These results are useful for the selection of the optimal reference gene required for high-precision measurements.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/42j7v246</guid>
      <pubDate>Thu, 17 Jul 2025 00:00:00 +0000</pubDate>
      <author>
        <name>YOKOYAMA, Toshifumi</name>
      </author>
      <author>
        <name>OMOTEHARA, Takuya</name>
      </author>
      <author>
        <name>HIRANO, Tetsushi</name>
      </author>
      <author>
        <name>KUBOTA, Naoto</name>
        <uri>https://orcid.org/0000-0003-0612-2300</uri>
      </author>
      <author>
        <name>YANAI, Shogo</name>
      </author>
      <author>
        <name>HASEGAWA, Chinatsu</name>
      </author>
      <author>
        <name>TAKADA, Tadashi</name>
      </author>
      <author>
        <name>MANTANI, Yohei</name>
      </author>
      <author>
        <name>HOSHI, Nobuhiko</name>
      </author>
    </item>
    <item>
      <title>Cerebrovascular alterations in a mouse model of late-onset Alzheimer’s disease</title>
      <link>https://escholarship.org/uc/item/2927t797</link>
      <description>Significance: Alzheimer's disease (AD) is an age-related neurodegenerative disorder with cerebrovascular alterations contributing to cognitive decline. Assessing cerebrovascular changes in mouse models that mimic the human condition of late-onset, sporadic AD is important for better human applicability.
Aim: To assess cerebrovascular changes in three mouse models: (1)&amp;nbsp;3xTg-AD; (2)&amp;nbsp;the humanized amyloid-beta knock-in (  -KI) mouse model of late-onset, sporadic AD; and (3)&amp;nbsp;age-matched wild-type mice.
Approach: We measured resting-state cerebral blood flow (CBF) and neurovascular coupling (NVC) using laser speckle imaging (LSI) and performed &lt;i&gt;ex vivo&lt;/i&gt; analyses of gene expression and cerebrovascular structure using bulk ribonucleic acid sequencing and confocal microscopy, respectively.
Results: Our study identifies specific cerebrovascular alterations in the  -KI mouse model, including increased resting-state CBF, a shift toward smaller blood vessel diameters,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2927t797</guid>
      <pubDate>Wed, 18 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Crouzet, Christian</name>
      </author>
      <author>
        <name>Xie, Danny F</name>
      </author>
      <author>
        <name>Nuqui, Maiella Nona Laquindanum</name>
      </author>
      <author>
        <name>Hasselman, Jonathan</name>
      </author>
      <author>
        <name>Phan, Thinh</name>
      </author>
      <author>
        <name>Wilson, Robert H</name>
      </author>
      <author>
        <name>Baglietto-Vargas, David</name>
      </author>
      <author>
        <name>Da Cunha, Celia</name>
      </author>
      <author>
        <name>Davtyan, Hayk</name>
      </author>
      <author>
        <name>Forner, Stefania</name>
      </author>
      <author>
        <name>Jullienne, Amandine</name>
      </author>
      <author>
        <name>Bazrafkan, Afsheen</name>
      </author>
      <author>
        <name>LaFerla, Frank M</name>
        <uri>https://orcid.org/0000-0003-2324-6911</uri>
      </author>
      <author>
        <name>Obenaus, Andre</name>
        <uri>https://orcid.org/0000-0003-0081-6950</uri>
      </author>
      <author>
        <name>Blurton-Jones, Mathew</name>
        <uri>https://orcid.org/0000-0002-7770-7157</uri>
      </author>
      <author>
        <name>Akbari, Yama</name>
        <uri>https://orcid.org/0000-0003-0729-5617</uri>
      </author>
      <author>
        <name>Green, Kim N</name>
        <uri>https://orcid.org/0000-0002-6049-6744</uri>
      </author>
      <author>
        <name>Choi, Bernard</name>
        <uri>https://orcid.org/0000-0002-4380-8291</uri>
      </author>
    </item>
    <item>
      <title>PTPN2 Regulates Iron Handling Protein Expression in Inflammatory Bowel Disease Patients and Prevents Iron Deficiency in Mice</title>
      <link>https://escholarship.org/uc/item/27g6g0wv</link>
      <description>Anemia is the most common extraintestinal manifestation of inflammatory bowel disease (IBD). Iron deficiency is the most frequent cause of anemia in IBD; however, the mechanisms involved are still poorly understood. Here, we investigated the role of the IBD risk gene, protein tyrosine phosphatase non-receptor type 2 (&lt;i&gt;PTPN2&lt;/i&gt;), in regulating iron homeostasis. Proteomic analyses were performed on serum from IBD patients genotyped for the IBD-associated loss-of-function rs1893217 &lt;i&gt;PTPN2&lt;/i&gt; variant. Constitutive &lt;i&gt;Ptpn2&lt;/i&gt; wild type (WT), heterozygous (Het), and knockout (KO) mice were analyzed for iron content, blood parameters, and expression of iron handling proteins. Iron absorption was assessed through radiotracer assays. Serum proteomic analyses revealed that the "iron homeostasis signaling pathway" was the main pathway downregulated in Crohn's disease (CD) patients carrying the &lt;i&gt;PTPN2&lt;/i&gt; risk allele, independent of disease activity. &lt;i&gt;Ptpn2&lt;/i&gt;-KO mice showed...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/27g6g0wv</guid>
      <pubDate>Sat, 26 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Lei, Hillmin</name>
      </author>
      <author>
        <name>Shawki, Ali</name>
      </author>
      <author>
        <name>Santos, Alina N</name>
      </author>
      <author>
        <name>Canale, Vinicius</name>
        <uri>https://orcid.org/0000-0002-2030-0268</uri>
      </author>
      <author>
        <name>Manz, Salomon</name>
      </author>
      <author>
        <name>Crawford, Meli’sa S</name>
      </author>
      <author>
        <name>Chatterjee, Pritha</name>
      </author>
      <author>
        <name>Spalinger, Marianne R</name>
      </author>
      <author>
        <name>Scharl, Michael</name>
      </author>
      <author>
        <name>McCole, Declan F</name>
        <uri>https://orcid.org/0000-0002-6286-0802</uri>
      </author>
    </item>
    <item>
      <title>Small RNA and Toll-like receptor interactions: origins and disease mechanisms.</title>
      <link>https://escholarship.org/uc/item/3cb4z4hj</link>
      <description>&lt;p&gt;Advances in small RNA sequencing have revealed diverse small noncoding RNAs (sncRNAs) beyond microRNAs (miRNAs), derived from transfer RNAs (tRNAs), ribosomal RNAs (rRNAs), small nuclear RNAs (snRNAs), and Y RNAs, carrying distinct RNA modifications. These emerging sncRNAs can function beyond RNA interference (RNAi), adopting aptamer-like roles by interacting with Toll-like receptors 7 and 8 (TLR7 and TLR8) via specific sequences, modifications, and structures. We propose a Sequential Activation Hypothesis where initial abnormal sncRNAs - triggered by infections or stresses - activate TLR7/8, leading to autoantibody production against autoantigens like RNA-binding proteins La and Ro. These autoantibody-antigen complexes further promote secondary immunogenic sncRNA production and repetitive TLR7/8 activation, perpetuating a vicious cycle sustaining autoimmunity. TLR7/8's X chromosome location and sex-biased expression contribute to female-dominant autoimmune diseases. Understanding...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3cb4z4hj</guid>
      <pubDate>Thu, 17 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Yu, Jiancheng</name>
      </author>
      <author>
        <name>Zhang, Xudong</name>
      </author>
      <author>
        <name>Cai, Chen</name>
      </author>
      <author>
        <name>Zhou, Tong</name>
      </author>
      <author>
        <name>Chen, Qi</name>
      </author>
    </item>
    <item>
      <title>Tofacitinib Mitigates the Increased SARS-CoV-2 Infection Susceptibility Caused by an IBD Risk Variant in the PTPN2 Gene</title>
      <link>https://escholarship.org/uc/item/8924m7xj</link>
      <description>BACKGROUND &amp;amp; AIMS: Coronavirus disease (COVID-19), caused by severe acquired respiratory syndrome-Coronavirus-2 (SARS-CoV-2), triggered a global pandemic with severe medical and socioeconomic consequences. Although fatality rates are higher among the elderly and those with underlying comorbidities, host factors that promote susceptibility to SARS-CoV-2 infection and severe disease are poorly understood. Although individuals with certain autoimmune/inflammatory disorders show increased susceptibility to viral infections, there is incomplete knowledge of SARS-CoV-2 susceptibility in these diseases. The aim of our study was to investigate whether the autoimmunity risk gene, PTPN2, which also confers elevated risk to develop inflammatory bowel disease, affects susceptibility to SARS-CoV-2 viral uptake.
METHODS: Using samples from PTPN2 genotyped patients with inflammatory bowel disease, PTPN2-deficient mice, and human intestinal and lung epithelial cell lines, we investigated...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8924m7xj</guid>
      <pubDate>Fri, 11 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Spalinger, Marianne R</name>
      </author>
      <author>
        <name>Sanati, Golshid</name>
      </author>
      <author>
        <name>Chatterjee, Pritha</name>
      </author>
      <author>
        <name>Hai, Rong</name>
      </author>
      <author>
        <name>Li, Jiang</name>
      </author>
      <author>
        <name>Santos, Alina N</name>
      </author>
      <author>
        <name>Nordgren, Tara M</name>
      </author>
      <author>
        <name>Tremblay, Michel L</name>
      </author>
      <author>
        <name>Eckmann, Lars</name>
      </author>
      <author>
        <name>Hanson, Elaine</name>
      </author>
      <author>
        <name>Scharl, Michael</name>
      </author>
      <author>
        <name>Wu, Xiwei</name>
      </author>
      <author>
        <name>Boland, Brigid S</name>
      </author>
      <author>
        <name>McCole, Declan F</name>
        <uri>https://orcid.org/0000-0002-6286-0802</uri>
      </author>
    </item>
    <item>
      <title>Mapping of promoter usage QTL using RNA-seq data reveals their contributions to complex traits</title>
      <link>https://escholarship.org/uc/item/0sh2j6xj</link>
      <description>Genomic variations are associated with gene expression levels, which are called expression quantitative trait loci (eQTL). Most eQTL may affect the total gene expression levels by regulating transcriptional activities of a specific promoter. However, the direct exploration of genomic loci associated with promoter activities using RNA-seq data has been challenging because eQTL analyses treat the total expression levels estimated by summing those of all isoforms transcribed from distinct promoters. Here we propose a new method for identifying genomic loci associated with promoter activities, called promoter usage quantitative trait loci (puQTL), using conventional RNA-seq data. By leveraging public RNA-seq datasets from the lymphoblastoid cell lines of 438 individuals from the GEUVADIS project, we obtained promoter activity estimates and mapped 2,592 puQTL at the 10% FDR level. The results of puQTL mapping enabled us to interpret the manner in which genomic variations regulate gene...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0sh2j6xj</guid>
      <pubDate>Fri, 4 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Kubota, Naoto</name>
        <uri>https://orcid.org/0000-0003-0612-2300</uri>
      </author>
      <author>
        <name>Suyama, Mikita</name>
      </author>
    </item>
    <item>
      <title>Shiba: a versatile computational method for systematic identification of differential RNA splicing across platforms</title>
      <link>https://escholarship.org/uc/item/0sm5691q</link>
      <description>Alternative pre-mRNA splicing (AS) is a fundamental regulatory process that generates transcript diversity and cell type variation. We developed Shiba, a comprehensive method that integrates transcript assembly, splicing event identification, read counting, and differential splicing analysis across RNA-seq platforms. Shiba excels in capturing annotated and unannotated AS events with superior accuracy, sensitivity, and reproducibility. It addresses the often-overlooked issue of junction read imbalance, significantly reducing false positives to aid target prioritization and downstream analyses. Unlike other tools that require large numbers of biological replicates or resulting in low sensitivity and high false positives, Shiba's statistics framework is agnostic to sample size, as demonstrated by simulated data and its effective application to real n=&amp;nbsp;1 RNA-seq datasets. To extend its utility to single-cell RNA-seq, we developed scShiba, which applies Shiba's pseudobulk approach...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0sm5691q</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Kubota, Naoto</name>
        <uri>https://orcid.org/0000-0003-0612-2300</uri>
      </author>
      <author>
        <name>Chen, Liang</name>
      </author>
      <author>
        <name>Zheng, Sika</name>
      </author>
    </item>
    <item>
      <title>Demyelination and neurodegeneration early in experimental autoimmune encephalomyelitis contribute to functional deficits in the anterior visual pathway</title>
      <link>https://escholarship.org/uc/item/8t1679b1</link>
      <description>Impaired visual function is a prevalent feature of optic neuritis&amp;nbsp;(ON) in multiple sclerosis (MS). Abnormal visual evoked potential (VEP) findings of increased latencies, reduced amplitudes and abnormal waveforms as well as decreased retinal nerve fiber layer (RNFL) assessed by optical coherence tomography (OCT) are hallmarks of ON-induced visual dysfunction. Here we utilized the experimental autoimmune encephalomyelitis (EAE) mouse model of MS to investigate the functional and pathological progression during early (before any clinical symptoms), peak (initial maximal clinical symptoms), and late (chronic disease for &amp;gt; 3&amp;nbsp;weeks) disease stages. Demyelination and initial stages of axon damage were observed in early EAE. Significant demyelination, inflammation, increased axon damage and impaired P1/N2 amplitudes and latencies by VEP were seen in middle and late EAE groups. A decrease in RNFL thickness by OCT was observed only during late EAE. NanoString analysis of optic...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8t1679b1</guid>
      <pubDate>Tue, 1 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Sekyi, Maria T</name>
      </author>
      <author>
        <name>Feri, Micah</name>
      </author>
      <author>
        <name>Desfor, Shane</name>
      </author>
      <author>
        <name>Atkinson, Kelley C</name>
      </author>
      <author>
        <name>Golestany, Batis</name>
      </author>
      <author>
        <name>Beltran, Fernando</name>
      </author>
      <author>
        <name>Tiwari-Woodruff, Seema K</name>
      </author>
    </item>
    <item>
      <title>Chronic, Low-Dose Methamphetamine Reveals Sexual Dimorphism of Memory Performance, Histopathology, and Gene Expression Affected by HIV-1 Tat Protein in a Transgenic Model of NeuroHIV</title>
      <link>https://escholarship.org/uc/item/7924f58g</link>
      <description>Methamphetamine (METH) use is frequent among people with HIV (PWH) and appears to increase the risk of neuronal injury and neurocognitive impairment (NCI). This study explored in vivo the effects of a 12 week (long-term), low-dose METH regimen in a transgenic animal model of neuroHIV with inducible expression of HIV-1 transactivator of transcription (Tat). Seven months after transient Tat induction and five months after METH exposure ended, we detected behavioral changes in the Barnes maze (BM) spatial memory task in the Tat and METH groups but not the combined Tat + METH group. The novel object recognition (NOR) task revealed that Tat extinguished discrimination in female animals with and without METH, although METH alone slightly improved NOR. In contrast, in males, Tat, METH, and Tat + METH all compromised NOR. Neuropathological examination detected sex-dependent and brain region-specific changes of pre-synaptic terminals, neurites, and activation of astrocytes and microglia....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7924f58g</guid>
      <pubDate>Thu, 13 Mar 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Harahap-Carrillo, Indira S</name>
      </author>
      <author>
        <name>Fok, Dominic</name>
      </author>
      <author>
        <name>Wong, Frances</name>
      </author>
      <author>
        <name>Malik, Gabriel</name>
      </author>
      <author>
        <name>Maung, Ricky</name>
      </author>
      <author>
        <name>Qiu, Xinru</name>
      </author>
      <author>
        <name>Ojeda-Juárez, Daniel</name>
      </author>
      <author>
        <name>Thaney, Victoria E</name>
      </author>
      <author>
        <name>Sanchez, Ana B</name>
      </author>
      <author>
        <name>Godzik, Adam</name>
      </author>
      <author>
        <name>Roberts, Amanda J</name>
      </author>
      <author>
        <name>Kaul, Marcus</name>
      </author>
    </item>
    <item>
      <title>Superstable lipid vacuoles endow cartilage with its shape and biomechanics</title>
      <link>https://escholarship.org/uc/item/0z5275h1</link>
      <description>Conventionally, the size, shape, and biomechanics of cartilages are determined by their voluminous extracellular matrix. By contrast, we found that multiple murine cartilages consist of lipid-filled cells called lipochondrocytes. Despite resembling adipocytes, lipochondrocytes were molecularly distinct and produced lipids exclusively through de novo lipogenesis. Consequently, lipochondrocytes grew uniform lipid droplets that resisted systemic lipid surges and did not enlarge upon obesity. Lipochondrocytes also lacked lipid mobilization factors, which enabled exceptional vacuole stability and protected cartilage from shrinking upon starvation. Lipid droplets modulated lipocartilage biomechanics by decreasing the tissue's stiffness, strength, and resilience. Lipochondrocytes were found in multiple mammals, including humans, but not in nonmammalian tetrapods. Thus, analogous to bubble wrap, superstable lipid vacuoles confer skeletal tissue with cartilage-like properties without "packing...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0z5275h1</guid>
      <pubDate>Wed, 29 Jan 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Ramos, Raul</name>
      </author>
      <author>
        <name>Pham, Kim T</name>
      </author>
      <author>
        <name>Prince, Richard C</name>
      </author>
      <author>
        <name>Leiser-Miller, Leith B</name>
      </author>
      <author>
        <name>Prasad, Maneeshi S</name>
      </author>
      <author>
        <name>Wang, Xiaojie</name>
        <uri>https://orcid.org/0000-0003-4817-5830</uri>
      </author>
      <author>
        <name>Nordberg, Rachel C</name>
        <uri>https://orcid.org/0000-0001-6047-6009</uri>
      </author>
      <author>
        <name>Bielajew, Benjamin J</name>
      </author>
      <author>
        <name>Hu, Jerry C</name>
      </author>
      <author>
        <name>Yamaga, Kosuke</name>
      </author>
      <author>
        <name>Oh, Ji Won</name>
      </author>
      <author>
        <name>Peng, Tao</name>
      </author>
      <author>
        <name>Datta, Rupsa</name>
      </author>
      <author>
        <name>Astrowskaja, Aksana</name>
      </author>
      <author>
        <name>Almet, Axel A</name>
      </author>
      <author>
        <name>Burns, John T</name>
      </author>
      <author>
        <name>Liu, Yuchen</name>
      </author>
      <author>
        <name>Guerrero-Juarez, Christian Fernando</name>
      </author>
      <author>
        <name>Tran, Bryant Q</name>
      </author>
      <author>
        <name>Chu, Yi-Lin</name>
      </author>
      <author>
        <name>Nguyen, Anh M</name>
      </author>
      <author>
        <name>Hsi, Tsai-Ching</name>
      </author>
      <author>
        <name>Lim, Norman T-L</name>
      </author>
      <author>
        <name>Schoeniger, Sandra</name>
      </author>
      <author>
        <name>Liu, Ruiqi</name>
      </author>
      <author>
        <name>Pai, Yun-Ling</name>
      </author>
      <author>
        <name>Vadivel, Chella K</name>
      </author>
      <author>
        <name>Ingleby, Sandy</name>
      </author>
      <author>
        <name>McKechnie, Andrew E</name>
      </author>
      <author>
        <name>van Breukelen, Frank</name>
      </author>
      <author>
        <name>Hoehn, Kyle L</name>
      </author>
      <author>
        <name>Rasweiler, John J</name>
      </author>
      <author>
        <name>Kohara, Michinori</name>
      </author>
      <author>
        <name>Loughry, William J</name>
      </author>
      <author>
        <name>Weldy, Scott H</name>
      </author>
      <author>
        <name>Cosper, Raymond</name>
      </author>
      <author>
        <name>Yang, Chao-Chun</name>
      </author>
      <author>
        <name>Lin, Sung-Jan</name>
      </author>
      <author>
        <name>Cooper, Kimberly L</name>
      </author>
      <author>
        <name>Santana, Sharlene E</name>
      </author>
      <author>
        <name>Bradley, Jeffrey E</name>
      </author>
      <author>
        <name>Kiebish, Michael A</name>
      </author>
      <author>
        <name>Digman, Michelle</name>
        <uri>https://orcid.org/0000-0003-4611-7100</uri>
      </author>
      <author>
        <name>James, David E</name>
      </author>
      <author>
        <name>Merrill, Amy E</name>
      </author>
      <author>
        <name>Nie, Qing</name>
        <uri>https://orcid.org/0000-0002-8804-3368</uri>
      </author>
      <author>
        <name>Schilling, Thomas F</name>
        <uri>https://orcid.org/0000-0003-1798-8695</uri>
      </author>
      <author>
        <name>Astrowski, Aliaksandr A</name>
      </author>
      <author>
        <name>Potma, Eric O</name>
        <uri>https://orcid.org/0000-0003-3916-6131</uri>
      </author>
      <author>
        <name>García-Castro, Martín I</name>
      </author>
      <author>
        <name>Athanasiou, Kyriacos A</name>
        <uri>https://orcid.org/0000-0001-5387-8405</uri>
      </author>
      <author>
        <name>Behringer, Richard R</name>
      </author>
      <author>
        <name>Plikus, Maksim V</name>
      </author>
    </item>
    <item>
      <title>Obesity Alters POMC and Kisspeptin Neuron Cross Talk Leading to Reduced Luteinizing Hormone in Male Mice</title>
      <link>https://escholarship.org/uc/item/70326624</link>
      <description>Obesity is associated with hypogonadism in males, characterized by low testosterone and sperm number. Previous studies determined that these stem from dysregulation of hypothalamic circuitry that regulates reproduction, by unknown mechanisms. Herein, we used mice fed chronic high-fat diet, which mimics human obesity, to determine mechanisms of impairment at the level of the hypothalamus, in particular gonadotropin-releasing hormone (GnRH) neurons that regulate luteinizing hormone (LH), which then regulates testosterone. Consistent with obese humans, we demonstrated lower LH, and lower pulse frequency of LH secretion, but unchanged pituitary responsiveness to GnRH. LH pulse frequency is regulated by pulsatile GnRH secretion, which is controlled by kisspeptin. Peripheral and central kisspeptin injections, and DREADD-mediated activation of kisspeptin neurons, demonstrated that kisspeptin neurons were suppressed in obese mice. Thus, we investigated regulators of kisspeptin secretion....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/70326624</guid>
      <pubDate>Wed, 22 Jan 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Villa, Pedro A</name>
      </author>
      <author>
        <name>Ruggiero-Ruff, Rebecca E</name>
      </author>
      <author>
        <name>Jamieson, Bradley B</name>
      </author>
      <author>
        <name>Campbell, Rebecca E</name>
      </author>
      <author>
        <name>Coss, Djurdjica</name>
        <uri>https://orcid.org/0000-0003-0692-1612</uri>
      </author>
    </item>
    <item>
      <title>Global atlas of predicted functional domains in Legionella pneumophila Dot/Icm translocated effectors</title>
      <link>https://escholarship.org/uc/item/8jm007mj</link>
      <description>Legionella pneumophila utilizes the Dot/Icm type IVB secretion system to deliver hundreds of effector proteins inside eukaryotic cells to ensure intracellular replication. Our understanding of the molecular functions of the largest pathogenic arsenal known to the bacterial world remains incomplete. By leveraging advancements in 3D protein structure prediction, we provide a comprehensive structural analysis of 368 L. pneumophila effectors, representing a global atlas of predicted functional domains summarized in a database (https://pathogens3d.org/legionella-pneumophila). Our analysis identified 157 types of diverse functional domains in 287 effectors, including 159 effectors with no prior functional annotations. Furthermore, we identified 35 cryptic domains in 30 effector models that have no similarity with experimentally structurally characterized proteins, thus, hinting at novel functionalities. Using this analysis, we demonstrate the activity of thirteen functional domains,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8jm007mj</guid>
      <pubDate>Mon, 20 Jan 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Patel, Deepak T</name>
      </author>
      <author>
        <name>Stogios, Peter J</name>
      </author>
      <author>
        <name>Jaroszewski, Lukasz</name>
      </author>
      <author>
        <name>Urbanus, Malene L</name>
      </author>
      <author>
        <name>Sedova, Mayya</name>
      </author>
      <author>
        <name>Semper, Cameron</name>
      </author>
      <author>
        <name>Le, Cathy</name>
      </author>
      <author>
        <name>Takkouche, Abraham</name>
      </author>
      <author>
        <name>Ichii, Keita</name>
      </author>
      <author>
        <name>Innabi, Julie</name>
      </author>
      <author>
        <name>Patel, Dhruvin H</name>
      </author>
      <author>
        <name>Ensminger, Alexander W</name>
      </author>
      <author>
        <name>Godzik, Adam</name>
      </author>
      <author>
        <name>Savchenko, Alexei</name>
      </author>
    </item>
    <item>
      <title>Alleviation of extensive visual pathway dysfunction by a remyelinating drug in a chronic mouse model of multiple sclerosis</title>
      <link>https://escholarship.org/uc/item/68m7s49c</link>
      <description>Visual deficits are among the most prevalent symptoms in patients with multiple sclerosis (MS). To understand deficits in the visual pathway during MS and potential treatment effects, we used experimental autoimmune encephalomyelitis (EAE), the most commonly used animal model of MS. The afferent visual pathway was assessed in vivo using optical coherence tomography (OCT), electroretinography (ERG), and visually evoked cortical potentials (VEPs). Inflammation, demyelination, and neurodegeneration were examined by immunohistochemistry ex vivo. In addition, an immunomodulatory, remyelinating agent, the estrogen receptor β ligand chloroindazole (IndCl), was tested for its therapeutic potential in the visual pathway. EAE produced functional deficits in visual system electrophysiology, including suppression of ERG and VEP waveform amplitudes and increased signal latencies. Therapeutic IndCl rescued overall visual system latency by VEP but had little impact on amplitude or ERG findings...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/68m7s49c</guid>
      <pubDate>Fri, 17 Jan 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Sekyi, Maria T</name>
      </author>
      <author>
        <name>Lauderdale, Kelli</name>
      </author>
      <author>
        <name>Atkinson, Kelley C</name>
      </author>
      <author>
        <name>Golestany, Batis</name>
      </author>
      <author>
        <name>Karim, Hawra</name>
      </author>
      <author>
        <name>Feri, Micah</name>
      </author>
      <author>
        <name>Soto, Joselyn S</name>
      </author>
      <author>
        <name>Diaz, Cobi</name>
      </author>
      <author>
        <name>Kim, Sung Hoon</name>
        <uri>https://orcid.org/0000-0002-3871-0847</uri>
      </author>
      <author>
        <name>Cilluffo, Marianne</name>
      </author>
      <author>
        <name>Nusinowitz, Steven</name>
      </author>
      <author>
        <name>Katzenellenbogen, John A</name>
      </author>
      <author>
        <name>Tiwari‐Woodruff, Seema K</name>
      </author>
    </item>
    <item>
      <title>Synthesis and Molecular Properties of Nerve Agent Reactivator HLö‑7 Dimethanesulfonate</title>
      <link>https://escholarship.org/uc/item/32t393kf</link>
      <description>The threat of a deliberate release of chemical nerve agents has underscored the need to continually improve field effective treatments for these types of poisonings. The oxime containing HLö-7 is a potential second-generation therapeutic reactivator. A synthetic process for HLö-7 is detailed with improvements to the DIBAL reduction and ion exchange steps. HLö-7 was visualized for the first time within the active site of human acetylcholinesterase and its relative &lt;i&gt;ex vivo&lt;/i&gt; potency confirmed against various nerve agents using a phrenic nerve hemidiaphragm assay.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/32t393kf</guid>
      <pubDate>Tue, 24 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Hsu, Fu-Lian</name>
      </author>
      <author>
        <name>Bae, Su Y</name>
      </author>
      <author>
        <name>McGuire, Jack</name>
      </author>
      <author>
        <name>Anderson, Dana R</name>
      </author>
      <author>
        <name>Bester, Stephanie M</name>
      </author>
      <author>
        <name>Height, Jude J</name>
      </author>
      <author>
        <name>Pegan, Scott D</name>
        <uri>https://orcid.org/0000-0002-2958-5319</uri>
      </author>
      <author>
        <name>Walz, Andrew J</name>
      </author>
    </item>
    <item>
      <title>Father’s diet influences son’s metabolic health through sperm RNA</title>
      <link>https://escholarship.org/uc/item/5c82w1sh</link>
      <description>DNA from organelles called mitochondria is not inherited from the father. But mitochondrial RNAs that sense paternal diet and mitochondrial quality are delivered from sperm to egg, affecting offspring metabolism.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5c82w1sh</guid>
      <pubDate>Mon, 16 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Cai, Chen</name>
      </author>
      <author>
        <name>Chen, Qi</name>
        <uri>https://orcid.org/0000-0001-6353-9589</uri>
      </author>
    </item>
    <item>
      <title>A Sexually Dimorphic Role for Intestinal Cannabinoid Receptor Subtype-1 in the Behavioral Expression of Anxiety</title>
      <link>https://escholarship.org/uc/item/4n32x2nx</link>
      <description>&lt;b&gt;Background:&lt;/b&gt; Increasing evidence suggests that the endocannabinoid system (ECS) in the brain controls anxiety and may be a therapeutic target for the treatment of anxiety disorders. For example, both pharmacological and genetic disruption of cannabinoid receptor subtype-1 (CB&lt;sub&gt;1&lt;/sub&gt;R) signaling in the central nervous system is associated with increased anxiety-like behaviors in rodents, while activating the system is anxiolytic. Sex is also a critical factor that controls the behavioral expression of anxiety; however, roles for the ECS in the gut in these processes and possible differences between sexes are largely unknown. &lt;b&gt;Objective:&lt;/b&gt; In this study, we aimed to determine if CB&lt;sub&gt;1&lt;/sub&gt;Rs in the intestinal epithelium exert control over anxiety-like behaviors in a sex-dependent manner. &lt;b&gt;Methods:&lt;/b&gt; We subjected male and female mice with conditional deletion of CB&lt;sub&gt;1&lt;/sub&gt;Rs in the intestinal epithelium (intCB&lt;sub&gt;1&lt;/sub&gt;&lt;sup&gt;-/-&lt;/sup&gt;) and controls (intCB&lt;sub&gt;1&lt;/sub&gt;&lt;sup&gt;+/+&lt;/sup&gt;)...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4n32x2nx</guid>
      <pubDate>Fri, 13 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Wood, Courtney P</name>
      </author>
      <author>
        <name>Avalos, Bryant</name>
      </author>
      <author>
        <name>Alvarez, Camila</name>
      </author>
      <author>
        <name>DiPatrizio, Nicholas V</name>
        <uri>https://orcid.org/0000-0001-8423-0695</uri>
      </author>
    </item>
    <item>
      <title>Replicon particle vaccination induces non-neutralizing anti-nucleoprotein antibody-mediated control of Crimean-Congo hemorrhagic fever virus</title>
      <link>https://escholarship.org/uc/item/4fr2f471</link>
      <description>Crimean-Congo hemorrhagic fever virus (CCHFV) can cause severe human disease and is considered a WHO priority pathogen due to the lack of efficacious vaccines and antivirals. A CCHF virus replicon particle (VRP) has previously shown protective efficacy in a lethal Ifnar-/- mouse model when administered as a single dose at least 3 days prior to challenge. Here, we determine that non-specific immune responses are not sufficient to confer short-term protection, since Lassa virus VRP vaccination 3 days prior to CCHFV challenge was not protective. We also investigate how CCHF VRP vaccination confers protective efficacy by examining viral kinetics, histopathology, clinical analytes and immunity early after challenge (3 and 6 days post infection) and compare to unvaccinated controls. We characterize how these effects differ based on vaccination period and correspond to previously reported CCHF VRP-mediated protection. Vaccinating Ifnar-/- mice with CCHF VRP 28, 14, 7, or 3 days prior...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4fr2f471</guid>
      <pubDate>Mon, 9 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Sorvillo, Teresa E</name>
      </author>
      <author>
        <name>Karaaslan, Elif</name>
      </author>
      <author>
        <name>Scholte, Florine EM</name>
      </author>
      <author>
        <name>Welch, Stephen R</name>
      </author>
      <author>
        <name>Coleman-McCray, JoAnn D</name>
      </author>
      <author>
        <name>Genzer, Sarah C</name>
      </author>
      <author>
        <name>Ritter, Jana M</name>
      </author>
      <author>
        <name>Hayes, Heather M</name>
      </author>
      <author>
        <name>Jain, Shilpi</name>
      </author>
      <author>
        <name>Pegan, Scott D</name>
        <uri>https://orcid.org/0000-0002-2958-5319</uri>
      </author>
      <author>
        <name>Bergeron, Éric</name>
      </author>
      <author>
        <name>Montgomery, Joel M</name>
      </author>
      <author>
        <name>Spiropoulou, Christina F</name>
      </author>
      <author>
        <name>Spengler, Jessica R</name>
      </author>
    </item>
    <item>
      <title>Elovanoids, a Novel Class of Lipid Mediators, Are Neuroprotective in a Traumatic Brain Injury Model in Rats</title>
      <link>https://escholarship.org/uc/item/28t2x6v0</link>
      <description>BACKGROUND: In the United States, traumatic brain injury (TBI) contributes significantly to mortality and morbidity. Elovanoids (ELVs), a novel class of homeostatic lipid mediators we recently discovered and characterized, have demonstrated neuroprotection in experimental stroke models but have never been tested after TBI.
METHODS: A moderate fluid-percussion injury (FPI) model was used on male rats that were treated with ELVs by intravenous (IV) or intranasal (IN) delivery. In addition, using liquid chromatography-mass spectrometry (LC-MS/MS), we examined whether ELVs could be detected in brain tissue after IN delivery.
RESULTS: ELVs administered intravenously 1 h after FPI improved behavior on days 2, 3, 7, and 14 by 20, 23, 31, and 34%, respectively, and preserved hippocampal CA3 and dentate gyrus (DG) volume loss compared to the vehicle. Whole-brain tractography revealed that ELV-IV treatment increased corpus callosum white matter fibers at the injury site. In comparison to...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/28t2x6v0</guid>
      <pubDate>Mon, 9 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Bazan, Nicolas G</name>
      </author>
      <author>
        <name>Obenaus, Andre</name>
        <uri>https://orcid.org/0000-0003-0081-6950</uri>
      </author>
      <author>
        <name>Khoutorova, Larissa</name>
      </author>
      <author>
        <name>Mukherjee, Pranab K</name>
      </author>
      <author>
        <name>Jun, Bokkyoo</name>
      </author>
      <author>
        <name>Semikov, Rostyslav</name>
      </author>
      <author>
        <name>Belayev, Ludmila</name>
      </author>
    </item>
    <item>
      <title>Structural characterization of protective non-neutralizing antibodies targeting Crimean-Congo hemorrhagic fever virus</title>
      <link>https://escholarship.org/uc/item/20h6k5qk</link>
      <description>Crimean-Congo Hemorrhagic Fever Virus (CCHFV) causes a life-threatening disease with up to a 40% mortality rate. With no approved medical countermeasures, CCHFV is considered a public health priority agent. The non-neutralizing mouse monoclonal antibody (mAb) 13G8 targets CCHFV glycoprotein GP38 and protects mice from lethal CCHFV challenge when administered prophylactically or therapeutically. Here, we reveal the structures of GP38 bound with a human chimeric 13G8 mAb and a newly isolated CC5-17 mAb from a human survivor. These mAbs bind overlapping epitopes with a shifted angle. The broad-spectrum potential of c13G8 and CC5-17 and the practicality of using them against Aigai virus, a closely related nairovirus were examined. Binding studies demonstrate that the presence of non-conserved amino acids in Aigai virus corresponding region prevent CCHFV mAbs from binding Aigai virus GP38. This information, coupled with in vivo efficacy, paves the way for future mAb therapeutics effective...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/20h6k5qk</guid>
      <pubDate>Mon, 9 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Durie, Ian A</name>
      </author>
      <author>
        <name>Tehrani, Zahra R</name>
      </author>
      <author>
        <name>Karaaslan, Elif</name>
      </author>
      <author>
        <name>Sorvillo, Teresa E</name>
      </author>
      <author>
        <name>McGuire, Jack</name>
      </author>
      <author>
        <name>Golden, Joseph W</name>
      </author>
      <author>
        <name>Welch, Stephen R</name>
      </author>
      <author>
        <name>Kainulainen, Markus H</name>
      </author>
      <author>
        <name>Harmon, Jessica R</name>
      </author>
      <author>
        <name>Mousa, Jarrod J</name>
      </author>
      <author>
        <name>Gonzalez, David</name>
      </author>
      <author>
        <name>Enos, Suzanne</name>
      </author>
      <author>
        <name>Koksal, Iftihar</name>
      </author>
      <author>
        <name>Yilmaz, Gurdal</name>
      </author>
      <author>
        <name>Karakoc, Hanife Nur</name>
      </author>
      <author>
        <name>Hamidi, Sanaz</name>
      </author>
      <author>
        <name>Albay, Cansu</name>
      </author>
      <author>
        <name>Spengler, Jessica R</name>
      </author>
      <author>
        <name>Spiropoulou, Christina F</name>
      </author>
      <author>
        <name>Garrison, Aura R</name>
      </author>
      <author>
        <name>Sajadi, Mohammad M</name>
      </author>
      <author>
        <name>Bergeron, Éric</name>
      </author>
      <author>
        <name>Pegan, Scott D</name>
        <uri>https://orcid.org/0000-0002-2958-5319</uri>
      </author>
    </item>
    <item>
      <title>Exploring Noncovalent Protease Inhibitors for the Treatment of Severe Acute Respiratory Syndrome and Severe Acute Respiratory Syndrome-Like Coronaviruses</title>
      <link>https://escholarship.org/uc/item/9v94r462</link>
      <description>Over the last 20 years, both severe acute respiratory syndrome coronavirus-1 and severe acute respiratory syndrome coronavirus-2 have transmitted from animal hosts to humans causing zoonotic outbreaks of severe disease. Both viruses originate from a group of betacoronaviruses known as subgroup 2b. The emergence of two dangerous human pathogens from this group along with previous studies illustrating the potential of other subgroup 2b members to transmit to humans has underscored the need for antiviral development against them. Coronaviruses modify the host innate immune response in part through the reversal of ubiquitination and ISGylation with their papain-like protease (PLpro). To identify unique or overarching subgroup 2b structural features or enzymatic biases, the PLpro from a subgroup 2b bat coronavirus, BtSCoV-Rf1.2004, was biochemically and structurally evaluated. This evaluation revealed that PLpros from subgroup 2b coronaviruses have narrow substrate specificity for...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9v94r462</guid>
      <pubDate>Sat, 7 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Freitas, Brendan T</name>
      </author>
      <author>
        <name>Ahiadorme, Daniil A</name>
      </author>
      <author>
        <name>Bagul, Rahul S</name>
      </author>
      <author>
        <name>Durie, Ian A</name>
      </author>
      <author>
        <name>Ghosh, Samir</name>
      </author>
      <author>
        <name>Hill, Jarvis</name>
      </author>
      <author>
        <name>Kramer, Naomi E</name>
      </author>
      <author>
        <name>Murray, Jackelyn</name>
      </author>
      <author>
        <name>O’Boyle, Brady M</name>
      </author>
      <author>
        <name>Onobun, Emmanuel</name>
      </author>
      <author>
        <name>Pirrone, Michael G</name>
      </author>
      <author>
        <name>Shepard, Justin D</name>
      </author>
      <author>
        <name>Enos, Suzanne</name>
      </author>
      <author>
        <name>Subedi, Yagya P</name>
      </author>
      <author>
        <name>Upadhyaya, Kapil</name>
      </author>
      <author>
        <name>Tripp, Ralph A</name>
      </author>
      <author>
        <name>Cummings, Brian S</name>
      </author>
      <author>
        <name>Crich, David</name>
      </author>
      <author>
        <name>Pegan, Scott D</name>
        <uri>https://orcid.org/0000-0002-2958-5319</uri>
      </author>
    </item>
    <item>
      <title>Polyphenols as alternative treatments of COVID-19</title>
      <link>https://escholarship.org/uc/item/1nx5058g</link>
      <description>Although scientists around the world have put lots of effort into the development of new treatments for COVID-19 since the outbreak, no drugs except Veklury (remdesivir) have been approved by FDA. There is an urgent need to discover some alternative antiviral treatment for COVID-19. Because polyphenols have been shown to possess antiviral activities, here we conducted a large-scale virtual screening for more than 400 polyphenols. Several lead compounds such as Petunidin 3-O-(6″-p-coumaroyl-glucoside) were identified to have promising binding affinities and convincing binding mechanisms. Analyzing the docking results and ADME properties sheds light on the potential efficacy of the top-ranked drug candidates and pinpoints the key residues on the target proteins for the future of drug development.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1nx5058g</guid>
      <pubDate>Sat, 7 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Wu, Yifei</name>
      </author>
      <author>
        <name>Pegan, Scott D</name>
        <uri>https://orcid.org/0000-0002-2958-5319</uri>
      </author>
      <author>
        <name>Crich, David</name>
      </author>
      <author>
        <name>Desrochers, Ellison</name>
      </author>
      <author>
        <name>Starling, Edward B</name>
      </author>
      <author>
        <name>Hansen, Madelyn C</name>
      </author>
      <author>
        <name>Booth, Carson</name>
      </author>
      <author>
        <name>Mullininx, Lauren Nicole</name>
      </author>
      <author>
        <name>Lou, Lei</name>
      </author>
      <author>
        <name>Chang, Kuan Y</name>
      </author>
      <author>
        <name>Xie, Zhong-Ru</name>
      </author>
    </item>
    <item>
      <title>The structural and biochemical impacts of monomerizing human acetylcholinesterase</title>
      <link>https://escholarship.org/uc/item/8dq1m0rj</link>
      <description>Serving a critical role in neurotransmission, human acetylcholinesterase (hAChE) is the target of organophosphate nerve agents. Hence, there is an active interest in studying the mechanism of inhibition and recovery of enzymatic activity, which could lead to better countermeasures against nerve agents. As hAChE is found in different oligomeric assemblies, certain approaches to studying it have been problematic. Herein, we examine the biochemical and structural impact of monomerizing hAChE by using two mutations: L380R/F535K. The activities of monomeric hAChE L380R/F535K and dimeric hAChE were determined to be comparable utilizing a modified Ellman's assay. To investigate the influence of subunit-subunit interactions on the structure of hAChE, a 2.1 Å X-ray crystallographic structure was determined. Apart from minor shifts along the dimer interface, the overall structure of the hAChE L380R/F535K mutant is similar to that of dimeric hAChE. To probe whether the plasticity of the...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8dq1m0rj</guid>
      <pubDate>Fri, 6 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Bester, Stephanie M</name>
      </author>
      <author>
        <name>Adipietro, Kaylin A</name>
      </author>
      <author>
        <name>Funk, Vanessa L</name>
      </author>
      <author>
        <name>Myslinski, James M</name>
      </author>
      <author>
        <name>Keul, Nicholas D</name>
      </author>
      <author>
        <name>Cheung, Jonah</name>
      </author>
      <author>
        <name>Wilder, Paul T</name>
      </author>
      <author>
        <name>Wood, Zachary A</name>
      </author>
      <author>
        <name>Weber, David J</name>
      </author>
      <author>
        <name>Height, Jude J</name>
      </author>
      <author>
        <name>Pegan, Scott D</name>
        <uri>https://orcid.org/0000-0002-2958-5319</uri>
      </author>
    </item>
    <item>
      <title>Changes in immune cell populations during acclimatization to high altitude.</title>
      <link>https://escholarship.org/uc/item/5xh8j8df</link>
      <description>The immune response to acute hypoxemia may play a critical role in high-altitude acclimatization and adaptation. However, if not properly controlled, hypoxemia-induced inflammation may exacerbate high-altitude pathologies, such as acute mountain sickness (AMS), or other hypoxia-related clinical conditions. Several studies report changes in immune cell subsets at high altitude. However, the mechanisms underlying these changes, and if these alterations are beneficial or maladaptive, remains unknown. To address this, we performed multiparameter flow cytometry on peripheral blood mononuclear cells (PBMCs) collected throughout 3 days of high-altitude acclimatization in healthy sea-level residents (n = 20). Additionally, we conducted in&amp;nbsp;vitro stimulation assays to test if high-altitude hypoxia exposure influences responses of immune cells to subsequent inflammatory stimuli. We found several immune populations were altered at high altitude, including monocytes, T cells, and B cells....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5xh8j8df</guid>
      <pubDate>Fri, 6 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Pham, Kathy</name>
      </author>
      <author>
        <name>Vargas, Abel</name>
      </author>
      <author>
        <name>Frost, Shyleen</name>
      </author>
      <author>
        <name>Shah, Saheli</name>
      </author>
      <author>
        <name>Heinrich, Erica</name>
      </author>
    </item>
    <item>
      <title>Identifying Drug Candidates for COVID-19 with Large-Scale Drug Screening</title>
      <link>https://escholarship.org/uc/item/5dk6s02q</link>
      <description>Papain-like protease (PL&lt;sup&gt;pro&lt;/sup&gt;) is critical to COVID-19 infection. Therefore, it is a significant target protein for drug development. We virtually screened a 26,193 compound library against the PL&lt;sup&gt;pro&lt;/sup&gt; of SARS-CoV-2 and identified several drug candidates with convincing binding affinities. The three best compounds all had better estimated binding energy than those of the drug candidates proposed in previous studies. By analyzing the docking results for the drug candidates identified in this and previous studies, we demonstrate that the critical interactions between the compounds and PL&lt;sup&gt;pro&lt;/sup&gt; proposed by the computational approaches are consistent with those proposed by the biological experiments. In addition, the predicted binding energies of the compounds in the dataset showed a similar trend as their IC&lt;sub&gt;50&lt;/sub&gt; values. The predicted ADME and drug-likeness properties also suggested that these identified compounds can be used for COVID-19 treatment.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5dk6s02q</guid>
      <pubDate>Fri, 6 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Wu, Yifei</name>
      </author>
      <author>
        <name>Pegan, Scott D</name>
        <uri>https://orcid.org/0000-0002-2958-5319</uri>
      </author>
      <author>
        <name>Crich, David</name>
      </author>
      <author>
        <name>Lou, Lei</name>
      </author>
      <author>
        <name>Mullininx, Lauren Nicole</name>
      </author>
      <author>
        <name>Starling, Edward B</name>
      </author>
      <author>
        <name>Booth, Carson</name>
      </author>
      <author>
        <name>Chishom, Andrew Edward</name>
      </author>
      <author>
        <name>Chang, Kuan Y</name>
      </author>
      <author>
        <name>Xie, Zhong-Ru</name>
      </author>
    </item>
    <item>
      <title>The SARS-CoV‑2 SSHHPS Recognized by the Papain-like Protease</title>
      <link>https://escholarship.org/uc/item/3r1357xw</link>
      <description>Viral proteases are highly specific and recognize conserved cleavage site sequences of ∼6-8 amino acids. Short stretches of homologous host-pathogen sequences (SSHHPS) can be found spanning the viral protease cleavage sites. We hypothesized that these sequences corresponded to specific host protein targets since &amp;gt;40 host proteins have been shown to be cleaved by Group IV viral proteases and one Group VI viral protease. Using PHI-BLAST and the viral protease cleavage site sequences, we searched the human proteome for host targets and analyzed the hit results. Although the polyprotein and host proteins related to the suppression of the innate immune responses may be the primary targets of these viral proteases, we identified other cleavable host proteins. These proteins appear to be related to the virus-induced phenotype associated with Group IV viruses, suggesting that information about viral pathogenesis may be extractable directly from the viral genome sequence. Here we identify...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3r1357xw</guid>
      <pubDate>Fri, 6 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Reynolds, Nathanael D</name>
      </author>
      <author>
        <name>Aceves, Nathalie M</name>
      </author>
      <author>
        <name>Liu, Jinny L</name>
      </author>
      <author>
        <name>Compton, Jaimee R</name>
      </author>
      <author>
        <name>Leary, Dagmar H</name>
      </author>
      <author>
        <name>Freitas, Brendan T</name>
      </author>
      <author>
        <name>Pegan, Scott D</name>
        <uri>https://orcid.org/0000-0002-2958-5319</uri>
      </author>
      <author>
        <name>Doctor, Katarina Z</name>
      </author>
      <author>
        <name>Wu, Fred Y</name>
      </author>
      <author>
        <name>Hu, Xin</name>
      </author>
      <author>
        <name>Legler, Patricia M</name>
      </author>
    </item>
    <item>
      <title>Inflammation associated with monocyte/macrophage activation and recruitment corresponds with lethal outcome in a mouse model of Crimean-Congo haemorrhagic fever</title>
      <link>https://escholarship.org/uc/item/0mk8g0qn</link>
      <description>Crimean-Congo haemorrhagic fever virus (CCHFV) causes human disease ranging from subclinical to a fatal haemorrhagic syndrome. Determinants of CCHF pathogenesis are largely unknown and animal models that recapitulate human disease are limited. A recently described mouse model uses a monoclonal antibody (mAb 5A3) targeting the interferon (IFN) alpha/beta receptor to suppress type I IFN responses, making animals transiently susceptible to infection. To advance utility of this model, we investigated effects of challenge route, timing of 5A3 delivery, mouse sex and age, and virus strain on clinical course and outcome. C57BL/6J mice received mAb 5A3 -1, 0, or -1/+1 days post-infection (dpi). Subsets were challenged with CCHFV strain Turkey04 or IbAr10200 subcutaneously or intraperitoneally, and serially euthanized 3- and 7-dpi, when meeting euthanasia criteria or at study completion (14 dpi). CCHFV-IbAr10200-infected mice almost uniformly succumbed to infection, whereas CCHFV-Turkey04-infected...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0mk8g0qn</guid>
      <pubDate>Fri, 6 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Sorvillo, Teresa E</name>
      </author>
      <author>
        <name>Ritter, Jana M</name>
      </author>
      <author>
        <name>Welch, Stephen R</name>
      </author>
      <author>
        <name>Coleman-McCray, JoAnn D</name>
      </author>
      <author>
        <name>Davies, Katherine A</name>
      </author>
      <author>
        <name>Hayes, Heather M</name>
      </author>
      <author>
        <name>Pegan, Scott D</name>
        <uri>https://orcid.org/0000-0002-2958-5319</uri>
      </author>
      <author>
        <name>Montgomery, Joel M</name>
      </author>
      <author>
        <name>Bergeron, Éric</name>
      </author>
      <author>
        <name>Spiropoulou, Christina F</name>
      </author>
      <author>
        <name>Spengler, Jessica R</name>
      </author>
    </item>
    <item>
      <title>tRNA renovatio: Rebirth through fragmentation</title>
      <link>https://escholarship.org/uc/item/00g0z278</link>
      <description>tRNA function is based on unique structures that enable mRNA decoding using anticodon trinucleotides. These structures interact with specific aminoacyl-tRNA synthetases and ribosomes using 3D shape and sequence signatures. Beyond translation, tRNAs serve as versatile signaling molecules interacting with other RNAs and proteins. Through evolutionary processes, tRNA fragmentation emerges as not merely random degradation but an act of recreation, generating specific shorter molecules called tRNA-derived small RNAs (tsRNAs). These tsRNAs exploit their linear sequences and newly arranged 3D structures for unexpected biological functions, epitomizing the tRNA "renovatio" (from Latin, meaning renewal, renovation, and rebirth). Emerging methods to uncover full tRNA/tsRNA sequences and modifications, combined with techniques to study RNA structures and to integrate AI-powered predictions, will enable comprehensive investigations of tRNA fragmentation products and new interaction potentials...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/00g0z278</guid>
      <pubDate>Thu, 28 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Kuhle, Bernhard</name>
      </author>
      <author>
        <name>Chen, Qi</name>
        <uri>https://orcid.org/0000-0001-6353-9589</uri>
      </author>
      <author>
        <name>Schimmel, Paul</name>
      </author>
    </item>
    <item>
      <title>The normal distribution of the hypoxic ventilatory response and methodological impacts: a meta‐analysis and computational investigation</title>
      <link>https://escholarship.org/uc/item/7f28b398</link>
      <description>The hypoxic ventilatory response (HVR) is the increase in breathing in response to reduced arterial oxygen pressure. Over several decades, studies have revealed substantial population-level differences in the magnitude of the HVR as well as significant inter-individual variation. In particular, low HVRs occur frequently in Andean high-altitude native populations. However, our group conducted hundreds of HVR measures over several years and commonly observed low responses in sea-level populations as well. As a result, we aimed to determine the normal HVR distribution, whether low responses were common, and to what extent variation in study protocols influence these findings. We conducted a comprehensive search of the literature and examined the distributions of HVR values across 78 studies that utilized step-down/steady-state or progressive hypoxia methods in untreated, healthy human subjects. Several studies included multiple datasets across different populations or experimental...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7f28b398</guid>
      <pubDate>Mon, 11 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Oeung, Britney</name>
      </author>
      <author>
        <name>Pham, Kathy</name>
      </author>
      <author>
        <name>Olfert, I Mark</name>
      </author>
      <author>
        <name>De La Zerda, David J</name>
      </author>
      <author>
        <name>Gaio, Eduardo</name>
      </author>
      <author>
        <name>Powell, Frank L</name>
      </author>
      <author>
        <name>Heinrich, Erica C</name>
      </author>
    </item>
    <item>
      <title>Protocol for the longitudinal study of neuroinflammation and reactive astrocytes in Lcn2CreERT2 mice</title>
      <link>https://escholarship.org/uc/item/0kw326tq</link>
      <description>During brain disease, astrocytes can reprogram into a reactive state that alters many of their functions. Here, we present a protocol for studying neuroinflammation and reactive astrogliosis in mice using lipopolysaccharide (LPS) from E.&amp;nbsp;coli. We describe steps for employing the Lcn2CreERT2 mouse crossed into a fluorescent Cre reporter line to label a subset of reactive astrocytes during and after inflammation. We then detail procedures for the longitudinal study of reactive astrocytes during the induction, progression, and/or resolution of astrogliosis. For complete details on the use and execution of this protocol, please refer to Agnew-Svoboda et&amp;nbsp;al.&lt;sup&gt;1&lt;/sup&gt;.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0kw326tq</guid>
      <pubDate>Mon, 11 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Ubina, Teresa</name>
        <uri>https://orcid.org/0000-0002-5549-4058</uri>
      </author>
      <author>
        <name>Agnew-Svoboda, William</name>
      </author>
      <author>
        <name>Figueroa, Zoe A</name>
      </author>
      <author>
        <name>Wilson, Emma H</name>
        <uri>https://orcid.org/0000-0002-6054-9981</uri>
      </author>
      <author>
        <name>Fiacco, Todd A</name>
      </author>
      <author>
        <name>Riccomagno, Martin M</name>
        <uri>https://orcid.org/0000-0002-1867-4439</uri>
      </author>
    </item>
    <item>
      <title>Early-life obesogenic environment integrates immunometabolic and epigenetic signatures governing neuroinflammation</title>
      <link>https://escholarship.org/uc/item/3505b7nz</link>
      <description>Childhood overweight/obesity is associated with stress-related psychopathology, yet the pathways connecting childhood obesity to stress susceptibility are poorly understood. We employed a systems biology approach with 62 adolescent Lewis rats fed a Western-like high-saturated fat diet (WD, 41% kcal from fat) or a control diet (CD, 13% kcal from fat). A subset of rats underwent a 31-day model of predator exposures and social instability (PSS). Effects were assessed using behavioral tests, DTI (diffusion tensor imaging), NODDI (neurite orientation dispersion and density imaging), 16S rRNA gene sequencing for gut microbiome profiling, hippocampal microglia analysis, and targeted gene methylation. Parallel experiments on human microglia cells (HMC3) examined how palmitic acid influences cortisol-related inflammatory responses. Rats exposed to WD and PSS exhibited deficits in sociability, increased fear/anxiety-like behaviors, food consumption, and body weight. WD/PSS altered hippocampal...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3505b7nz</guid>
      <pubDate>Fri, 8 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Ontiveros-Ángel, Perla</name>
      </author>
      <author>
        <name>Vega-Torres, Julio David</name>
      </author>
      <author>
        <name>Simon, Timothy B</name>
      </author>
      <author>
        <name>Williams, Vivianna</name>
      </author>
      <author>
        <name>Inostroza-Nives, Yaritza</name>
      </author>
      <author>
        <name>Alvarado-Crespo, Nashareth</name>
      </author>
      <author>
        <name>Gonzalez, Yarimar Vega</name>
      </author>
      <author>
        <name>Pompolius, Marjory</name>
      </author>
      <author>
        <name>Katzka, William</name>
      </author>
      <author>
        <name>Lou, John</name>
      </author>
      <author>
        <name>Sharafeddin, Fransua</name>
      </author>
      <author>
        <name>De la Peña, Ike</name>
      </author>
      <author>
        <name>Dong, Tien</name>
        <uri>https://orcid.org/0000-0003-0105-8063</uri>
      </author>
      <author>
        <name>Gupta, Arpana</name>
      </author>
      <author>
        <name>Viet, Chi T</name>
      </author>
      <author>
        <name>Febo, Marcelo</name>
      </author>
      <author>
        <name>Obenaus, Andre</name>
        <uri>https://orcid.org/0000-0003-0081-6950</uri>
      </author>
      <author>
        <name>Nair, Aarti</name>
      </author>
      <author>
        <name>Figueroa, Johnny D</name>
      </author>
    </item>
    <item>
      <title>EphB2 Signaling Is Implicated in Astrocyte-Mediated Parvalbumin Inhibitory Synapse Development</title>
      <link>https://escholarship.org/uc/item/8qd430n4</link>
      <description>Impaired inhibitory synapse development is suggested to drive neuronal hyperactivity in autism spectrum disorders (ASD) and epilepsy. We propose a novel mechanism by which astrocytes control the development of parvalbumin (PV)-specific inhibitory synapses in the hippocampus, implicating ephrin-B/EphB signaling. Here, we utilize genetic approaches to assess functional and structural connectivity between PV and pyramidal cells (PCs) through whole-cell patch-clamp electrophysiology, optogenetics, immunohistochemical analysis, and behaviors in male and female mice. While inhibitory synapse development is adversely affected by PV-specific expression of EphB2, a strong candidate ASD risk gene, astrocytic ephrin-B1 facilitates PV→PC connectivity through a mechanism involving EphB signaling in PV boutons. In contrast, the loss of astrocytic ephrin-B1 reduces PV→PC connectivity and inhibition, resulting in increased seizure susceptibility and an ASD-like phenotype. Our findings underscore...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8qd430n4</guid>
      <pubDate>Thu, 7 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Sutley-Koury, Samantha N</name>
      </author>
      <author>
        <name>Taitano-Johnson, Christopher</name>
      </author>
      <author>
        <name>Kulinich, Anna O</name>
      </author>
      <author>
        <name>Farooq, Nadia</name>
      </author>
      <author>
        <name>Wagner, Victoria A</name>
      </author>
      <author>
        <name>Robles, Marissa</name>
      </author>
      <author>
        <name>Hickmott, Peter W</name>
      </author>
      <author>
        <name>Santhakumar, Vijayalakshmi</name>
        <uri>https://orcid.org/0000-0001-6278-4187</uri>
      </author>
      <author>
        <name>Mimche, Patrice N</name>
      </author>
      <author>
        <name>Ethell, Iryna M</name>
        <uri>https://orcid.org/0000-0002-1324-6611</uri>
      </author>
    </item>
    <item>
      <title>Functional consequences of postnatal interventions in a mouse model of Fragile X syndrome</title>
      <link>https://escholarship.org/uc/item/7sx65717</link>
      <description>BACKGROUND: Fragile X syndrome (FXS) is a leading genetic cause of autism and intellectual disability with cortical hyperexcitability and sensory hypersensitivity attributed to loss and hypofunction of inhibitory parvalbumin-expressing (PV) cells. Our studies provide novel insights into the role of excitatory neurons in abnormal development of PV cells during a postnatal period of inhibitory circuit refinement.
METHODS: To achieve Fragile X mental retardation gene (Fmr1) deletion and re-expression in excitatory neurons during the postnatal day (P)14-P21 period, we generated Cre&lt;sup&gt;CaMKIIa&lt;/sup&gt;/Fmr1&lt;sup&gt;Flox/y&lt;/sup&gt; (cOFF) and Cre&lt;sup&gt;CaMKIIa&lt;/sup&gt;/Fmr1&lt;sup&gt;FloxNeo/y&lt;/sup&gt; (cON) mice, respectively. Cortical phenotypes were evaluated in adult mice using biochemical, cellular, clinically relevant electroencephalogram (EEG) and behavioral tests.
RESULTS: We found that similar to global Fmr1 KO mice, the density of PV-expressing cells, their activation, and sound-evoked gamma synchronization...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7sx65717</guid>
      <pubDate>Thu, 7 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Rais, Maham</name>
      </author>
      <author>
        <name>Lovelace, Jonathan W</name>
      </author>
      <author>
        <name>Shuai, Xinghao S</name>
      </author>
      <author>
        <name>Woodard, Walker</name>
      </author>
      <author>
        <name>Bishay, Steven</name>
      </author>
      <author>
        <name>Estrada, Leo</name>
      </author>
      <author>
        <name>Sharma, Ashwin R</name>
      </author>
      <author>
        <name>Nguy, Austin</name>
      </author>
      <author>
        <name>Kulinich, Anna</name>
      </author>
      <author>
        <name>Pirbhoy, Patricia S</name>
      </author>
      <author>
        <name>Palacios, Arnold R</name>
      </author>
      <author>
        <name>Nelson, David L</name>
      </author>
      <author>
        <name>Razak, Khaleel A</name>
      </author>
      <author>
        <name>Ethell, Iryna M</name>
        <uri>https://orcid.org/0000-0002-1324-6611</uri>
      </author>
    </item>
    <item>
      <title>Urokinase plasminogen activator mediates changes in human astrocytes modeling fragile X syndrome</title>
      <link>https://escholarship.org/uc/item/2k90c0dv</link>
      <description>The function of astrocytes intertwines with the extracellular matrix, whose neuron and glial cell-derived components shape neuronal plasticity. Astrocyte abnormalities have been reported in the brain of the mouse model for fragile X syndrome (FXS), the most common cause of inherited intellectual disability, and a monogenic cause of autism spectrum disorder. We compared human FXS and control astrocytes generated from human induced pluripotent stem cells and we found increased expression of urokinase plasminogen activator (uPA), which modulates degradation of extracellular matrix. Several pathways associated with uPA and its receptor function were activated in FXS astrocytes. Levels of uPA were also increased in conditioned medium collected from FXS hiPSC-derived astrocyte cultures and correlated inversely with intracellular Ca&lt;sup&gt;2+&lt;/sup&gt; responses to activation of L-type voltage-gated calcium channels in human astrocytes. Increased uPA augmented neuronal phosphorylation of TrkB...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2k90c0dv</guid>
      <pubDate>Thu, 7 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Peteri, Ulla‐Kaisa</name>
      </author>
      <author>
        <name>Pitkonen, Juho</name>
      </author>
      <author>
        <name>de Toma, Ilario</name>
      </author>
      <author>
        <name>Nieminen, Otso</name>
      </author>
      <author>
        <name>Utami, Kagistia Hana</name>
      </author>
      <author>
        <name>Strandin, Tomas M</name>
      </author>
      <author>
        <name>Corcoran, Padraic</name>
      </author>
      <author>
        <name>Roybon, Laurent</name>
      </author>
      <author>
        <name>Vaheri, Antti</name>
      </author>
      <author>
        <name>Ethell, Iryna</name>
        <uri>https://orcid.org/0000-0002-1324-6611</uri>
      </author>
      <author>
        <name>Casarotto, Plinio</name>
      </author>
      <author>
        <name>Pouladi, Mahmoud A</name>
      </author>
      <author>
        <name>Castrén, Maija L</name>
      </author>
    </item>
    <item>
      <title>Editorial: Neural markers of sensory processing in development</title>
      <link>https://escholarship.org/uc/item/2b07n7r8</link>
      <description>Editorial: Neural markers of sensory processing in development</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2b07n7r8</guid>
      <pubDate>Thu, 7 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Ethridge, Lauren E</name>
      </author>
      <author>
        <name>Auerbach, Benjamin D</name>
      </author>
      <author>
        <name>Contractor, Anis</name>
      </author>
      <author>
        <name>Ethell, Iryna M</name>
        <uri>https://orcid.org/0000-0002-1324-6611</uri>
      </author>
      <author>
        <name>McCullagh, Elizabeth A</name>
      </author>
      <author>
        <name>Pedapati, Ernest V</name>
      </author>
    </item>
    <item>
      <title>Astrocytic Ephrin-B1 Regulates Oligodendrocyte Development and Myelination</title>
      <link>https://escholarship.org/uc/item/1hv069b2</link>
      <description>Astrocytes have been implicated in oligodendrocyte development and myelination, however, the mechanisms by which astrocytes regulate oligodendrocytes remain unclear. Our findings suggest a new mechanism that regulates astrocyte-mediated oligodendrocyte development through ephrin-B1 signaling in astrocytes. Using a mouse model, we examined the role of astrocytic ephrin-B1 signaling in oligodendrocyte development by deleting ephrin-B1 specifically in astrocytes during the postnatal days (P)14-P28 period and used mRNA analysis, immunohistochemistry, and mouse behaviors to study its effects on oligodendrocytes and myelination. We found that deletion of astrocytic ephrin-B1 downregulated many genes associated with oligodendrocyte development, myelination, and lipid metabolism in the hippocampus and the corpus callosum. Additionally, we observed a reduced number of oligodendrocytes and impaired myelination in the corpus callosum of astrocyte-specific ephrin-B1 KO mice. Finally, our...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1hv069b2</guid>
      <pubDate>Thu, 7 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Sutley-Koury, Samantha N</name>
      </author>
      <author>
        <name>Anderson, Alyssa</name>
      </author>
      <author>
        <name>Taitano-Johnson, Christopher</name>
      </author>
      <author>
        <name>Ajayi, Moyinoluwa</name>
      </author>
      <author>
        <name>Kulinich, Anna O</name>
      </author>
      <author>
        <name>Contreras, Kimberly</name>
      </author>
      <author>
        <name>Regalado, Jasmin</name>
      </author>
      <author>
        <name>Tiwari-Woodruff, Seema K</name>
      </author>
      <author>
        <name>Ethell, Iryna M</name>
        <uri>https://orcid.org/0000-0002-1324-6611</uri>
      </author>
    </item>
    <item>
      <title>Mass Spectrometry-Based Direct Sequencing of tRNAs De Novo and Quantitative Mapping of Multiple RNA Modifications</title>
      <link>https://escholarship.org/uc/item/08x970sr</link>
      <description>Despite the extensive use of next-generation sequencing (NGS) of RNA, simultaneous direct sequencing and quantitative mapping of multiple RNA nucleotide modifications remains challenging. Mass spectrometry (MS)-based sequencing can directly sequence all RNA modifications without being limited to specific ones, but it requires a perfect MS ladder that few tRNAs can provide. Here, we describe an MS ladder complementation sequencing approach (MLC-Seq) that circumvents the perfect ladder requirement, allowing de novo MS sequencing of full-length heterogeneous cellular tRNAs with multiple nucleotide modifications at single-nucleotide precision. Unlike NGS-based methods, which lose RNA modification information, MLC-Seq preserves RNA sequence diversity and modification information, revealing new detailed stoichiometric tRNA modification profiles and their changes upon treatment with the dealkylating enzyme AlkB. It can also be combined with reference sequences to provide quantitative...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/08x970sr</guid>
      <pubDate>Tue, 5 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Yuan, Xiaohong</name>
      </author>
      <author>
        <name>Su, Yue</name>
      </author>
      <author>
        <name>Johnson, Benjamin</name>
      </author>
      <author>
        <name>Kirchner, Michele</name>
      </author>
      <author>
        <name>Zhang, Xudong</name>
      </author>
      <author>
        <name>Xu, Sihang</name>
      </author>
      <author>
        <name>Jiang, Sophia</name>
      </author>
      <author>
        <name>Wu, Jing</name>
      </author>
      <author>
        <name>Shi, Shundi</name>
      </author>
      <author>
        <name>Russo, James J</name>
      </author>
      <author>
        <name>Chen, Qi</name>
        <uri>https://orcid.org/0000-0001-6353-9589</uri>
      </author>
      <author>
        <name>Zhang, Shenglong</name>
      </author>
    </item>
    <item>
      <title>Crimean Congo hemorrhagic fever virus nucleoprotein and GP38 subunit vaccine combination prevents morbidity in mice</title>
      <link>https://escholarship.org/uc/item/1ff7g8vn</link>
      <description>Immunizing mice with Crimean-Congo hemorrhagic fever virus (CCHFV) nucleoprotein (NP), glycoprotein precursor (GPC), or with the GP38 domain of GPC, can be protective when the proteins are delivered with viral vectors or as a DNA or RNA vaccine. Subunit vaccines are a safe and cost-effective alternative to some vaccine platforms, but Gc and Gn glycoprotein subunit vaccines for CCHFV fail to protect despite eliciting high levels of neutralizing antibodies. Here, we investigated humoral and cellular immune responses and the protective efficacy of recombinant NP, GP38, and GP38 forms (GP85 and GP160) associated with the highly glycosylated mucin-like (MLD) domain, as well as the NP + GP38 combination. Vaccination with GP160, GP85, or GP38 did not confer protection, and vaccination with the MLD-associated GP38 forms blunted the humoral immune responses to GP38, worsened clinical chemistry, and increased viral RNA in the blood compared to the GP38 vaccination. In contrast, NP vaccination...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1ff7g8vn</guid>
      <pubDate>Thu, 19 Sep 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Karaaslan, Elif</name>
      </author>
      <author>
        <name>Sorvillo, Teresa E</name>
      </author>
      <author>
        <name>Scholte, Florine EM</name>
      </author>
      <author>
        <name>O’Neal, Troy Justin</name>
      </author>
      <author>
        <name>Welch, Stephen R</name>
      </author>
      <author>
        <name>Davies, Katherine A</name>
      </author>
      <author>
        <name>Coleman-McCray, JoAnn D</name>
      </author>
      <author>
        <name>Harmon, Jessica R</name>
      </author>
      <author>
        <name>Ritter, Jana M</name>
      </author>
      <author>
        <name>Pegan, Scott D</name>
        <uri>https://orcid.org/0000-0002-2958-5319</uri>
      </author>
      <author>
        <name>Montgomery, Joel M</name>
      </author>
      <author>
        <name>Spengler, Jessica R</name>
      </author>
      <author>
        <name>Spiropoulou, Christina F</name>
      </author>
      <author>
        <name>Bergeron, Éric</name>
      </author>
    </item>
    <item>
      <title>Myt1l safeguards neuronal identity by actively repressing many non-neuronal fates</title>
      <link>https://escholarship.org/uc/item/8bz168xd</link>
      <description>The neuron-specific transcription factor Myt1l represses many somatic lineage programs, but not the neuronal lineage program, to both induce and maintain neuronal identity.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8bz168xd</guid>
      <pubDate>Fri, 6 Sep 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Mall, Moritz</name>
      </author>
      <author>
        <name>Kareta, Michael S</name>
      </author>
      <author>
        <name>Chanda, Soham</name>
      </author>
      <author>
        <name>Ahlenius, Henrik</name>
      </author>
      <author>
        <name>Perotti, Nicholas</name>
      </author>
      <author>
        <name>Zhou, Bo</name>
      </author>
      <author>
        <name>Grieder, Sarah D</name>
      </author>
      <author>
        <name>Ge, Xuecai</name>
      </author>
      <author>
        <name>Drake, Sienna</name>
      </author>
      <author>
        <name>Euong Ang, Cheen</name>
      </author>
      <author>
        <name>Walker, Brandon M</name>
      </author>
      <author>
        <name>Vierbuchen, Thomas</name>
      </author>
      <author>
        <name>Fuentes, Daniel R</name>
      </author>
      <author>
        <name>Brennecke, Philip</name>
      </author>
      <author>
        <name>Nitta, Kazuhiro R</name>
      </author>
      <author>
        <name>Jolma, Arttu</name>
      </author>
      <author>
        <name>Steinmetz, Lars M</name>
      </author>
      <author>
        <name>Taipale, Jussi</name>
      </author>
      <author>
        <name>Südhof, Thomas C</name>
      </author>
      <author>
        <name>Wernig, Marius</name>
      </author>
    </item>
    <item>
      <title>Development of mouse preimplantation embryos in space</title>
      <link>https://escholarship.org/uc/item/80b518tk</link>
      <description>The development of life beyond planet Earth is a long-standing quest of the human race, but whether normal mammalian embryonic development can occur in space is still unclear. Here, we show unequivocally that preimplantation mouse embryos can develop in space, but the rate of blastocyst formation and blastocyst quality are compromised. Additionally, the cells in the embryo contain severe DNA damage, while the genome of the blastocysts developed in space is globally hypomethylated with a unique set of differentially methylated regions. The developmental defects, DNA damage and epigenetic abnormalities can be largely mimicked by the treatment with ground-based low-dose radiation. However, the exposure to simulated microgravity alone does not cause major disruptions of embryonic development, indicating that radiation is the main cause for the developmental defects. This work advances the understanding of embryonic development in space and reveals long-term extreme low-dose radiation...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/80b518tk</guid>
      <pubDate>Fri, 6 Sep 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Lei, Xiaohua</name>
      </author>
      <author>
        <name>Cao, Yujing</name>
      </author>
      <author>
        <name>Ma, Baohua</name>
      </author>
      <author>
        <name>Zhang, Yunfang</name>
      </author>
      <author>
        <name>Ning, Lina</name>
      </author>
      <author>
        <name>Qian, Jingjing</name>
      </author>
      <author>
        <name>Zhang, Liwen</name>
      </author>
      <author>
        <name>Qu, Yongcun</name>
      </author>
      <author>
        <name>Zhang, Tao</name>
      </author>
      <author>
        <name>Li, Dehong</name>
      </author>
      <author>
        <name>Chen, Qi</name>
        <uri>https://orcid.org/0000-0001-6353-9589</uri>
      </author>
      <author>
        <name>Shi, Junchao</name>
      </author>
      <author>
        <name>Zhang, Xudong</name>
      </author>
      <author>
        <name>Ma, Chiyuan</name>
      </author>
      <author>
        <name>Zhang, Ying</name>
      </author>
      <author>
        <name>Duan, Enkui</name>
      </author>
    </item>
    <item>
      <title>CircFunBase: a database for functional circular RNAs</title>
      <link>https://escholarship.org/uc/item/7zv9j98j</link>
      <description>Increasing evidence reveals that circular RNAs (circRNAs) are widespread in eukaryotes and play important roles in diverse biological processes. However, a comprehensive functionally annotated circRNA database is still lacking. CircFunBase is a web-accessible database that aims to provide a high-quality functional circRNA resource including experimentally validated and computationally predicted functions. The current version of CircFunBase documents more than 7000 manually curated functional circRNA entries, mainly including Homo sapiens, Mus musculus etc. CircFunBase provides visualized circRNA-miRNA interaction networks. In addition, a genome browser is provided to visualize the genome context of circRNAs. As a biological information platform for circRNAs, CircFunBase will contribute for circRNA studies and bridge the gap between circRNAs and their functions.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7zv9j98j</guid>
      <pubDate>Fri, 6 Sep 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Meng, Xianwen</name>
      </author>
      <author>
        <name>Hu, Dahui</name>
      </author>
      <author>
        <name>Zhang, Peijing</name>
      </author>
      <author>
        <name>Chen, Qi</name>
        <uri>https://orcid.org/0000-0001-6353-9589</uri>
      </author>
      <author>
        <name>Chen, Ming</name>
      </author>
    </item>
    <item>
      <title>Molecular carriers of acquired inheritance: absence of evidence is not evidence of absence</title>
      <link>https://escholarship.org/uc/item/5gp7r1gp</link>
      <description>&lt;i&gt;In utero&lt;/i&gt; exposure to environmental endocrine disruptors can cause transgenerational effects in the males of subsequent generations. DNA methylation (5 mC) was suggested, but being challenged as the molecular carrier of such epigenetic information. In a recent study, Schuster &lt;i&gt;et al.&lt;/i&gt; show a changed small RNA profile changed in the sperm of F3 generation after F0 &lt;i&gt;in utero&lt;/i&gt; vinclozolin exposure, suggesting additional transgenerational epigenetic carriers for endocrine disruptor effects, other than DNA methylation.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5gp7r1gp</guid>
      <pubDate>Fri, 6 Sep 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Shi, Junchao</name>
      </author>
      <author>
        <name>Zhang, Yunfang</name>
      </author>
      <author>
        <name>Chen, Qi</name>
        <uri>https://orcid.org/0000-0001-6353-9589</uri>
      </author>
    </item>
    <item>
      <title>Non-Coding RNAs and their Integrated Networks</title>
      <link>https://escholarship.org/uc/item/5g39d0vq</link>
      <description>Eukaryotic genomes are pervasively transcribed. Besides protein-coding RNAs, there are different types of non-coding RNAs that modulate complex molecular and cellular processes. RNA sequencing technologies and bioinformatics methods greatly promoted the study of ncRNAs, which revealed ncRNAs' essential roles in diverse aspects of biological functions. As important key players in gene regulatory networks, ncRNAs work with other biomolecules, including coding and non-coding RNAs, DNAs and proteins. In this review, we discuss the distinct types of ncRNAs, including housekeeping ncRNAs and regulatory ncRNAs, their versatile functions and interactions, transcription, translation, and modification. Moreover, we summarize the integrated networks of ncRNA interactions, providing a comprehensive landscape of ncRNAs regulatory roles.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5g39d0vq</guid>
      <pubDate>Fri, 6 Sep 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Zhang, Peijing</name>
      </author>
      <author>
        <name>Wu, Wenyi</name>
      </author>
      <author>
        <name>Chen, Qi</name>
        <uri>https://orcid.org/0000-0001-6353-9589</uri>
      </author>
      <author>
        <name>Chen, Ming</name>
      </author>
    </item>
    <item>
      <title>Characterization and structural basis of a lethal mouse-adapted SARS-CoV-2</title>
      <link>https://escholarship.org/uc/item/5cp4r84c</link>
      <description>There is an urgent need for animal models to study SARS-CoV-2 pathogenicity. Here, we generate and characterize a novel mouse-adapted SARS-CoV-2 strain, MASCp36, that causes severe respiratory symptoms, and mortality. Our model exhibits age- and gender-related mortality akin to severe COVID-19. Deep sequencing identified three amino acid substitutions, N501Y, Q493H, and K417N, at the receptor binding domain (RBD) of MASCp36, during in vivo passaging. All three RBD mutations significantly enhance binding affinity to its endogenous receptor, ACE2. Cryo-electron microscopy analysis of human ACE2 (hACE2), or mouse ACE2 (mACE2), in complex with the RBD of MASCp36, at 3.1 to 3.7 Å resolution, reveals the molecular basis for the receptor-binding switch. N501Y and Q493H enhance the binding affinity to hACE2, whereas triple mutations at N501Y/Q493H/K417N decrease affinity and reduce infectivity of MASCp36. Our study provides a platform for studying SARS-CoV-2 pathogenesis, and unveils...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5cp4r84c</guid>
      <pubDate>Fri, 6 Sep 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Sun, Shihui</name>
      </author>
      <author>
        <name>Gu, Hongjing</name>
      </author>
      <author>
        <name>Cao, Lei</name>
      </author>
      <author>
        <name>Chen, Qi</name>
        <uri>https://orcid.org/0000-0001-6353-9589</uri>
      </author>
      <author>
        <name>Ye, Qing</name>
      </author>
      <author>
        <name>Yang, Guan</name>
      </author>
      <author>
        <name>Li, Rui-Ting</name>
      </author>
      <author>
        <name>Fan, Hang</name>
      </author>
      <author>
        <name>Deng, Yong-Qiang</name>
      </author>
      <author>
        <name>Song, Xiaopeng</name>
      </author>
      <author>
        <name>Qi, Yini</name>
      </author>
      <author>
        <name>Li, Min</name>
      </author>
      <author>
        <name>Lan, Jun</name>
      </author>
      <author>
        <name>Feng, Rui</name>
      </author>
      <author>
        <name>Guo, Yan</name>
      </author>
      <author>
        <name>Zhu, Na</name>
      </author>
      <author>
        <name>Qin, Si</name>
      </author>
      <author>
        <name>Wang, Lei</name>
      </author>
      <author>
        <name>Zhang, Yi-Fei</name>
      </author>
      <author>
        <name>Zhou, Chao</name>
      </author>
      <author>
        <name>Zhao, Lingna</name>
      </author>
      <author>
        <name>Chen, Yuehong</name>
      </author>
      <author>
        <name>Shen, Meng</name>
      </author>
      <author>
        <name>Cui, Yujun</name>
      </author>
      <author>
        <name>Yang, Xiao</name>
      </author>
      <author>
        <name>Wang, Xinquan</name>
      </author>
      <author>
        <name>Tan, Wenjie</name>
      </author>
      <author>
        <name>Wang, Hui</name>
      </author>
      <author>
        <name>Wang, Xiangxi</name>
      </author>
      <author>
        <name>Qin, Cheng-Feng</name>
      </author>
    </item>
    <item>
      <title>Identification and characterization of ncRNA-associated ceRNA networks in Arabidopsis leaf development</title>
      <link>https://escholarship.org/uc/item/4cd8r2tc</link>
      <description>BackgroundLeaf development is a complex biological process that is accompanied by wide transcriptional changes. Many protein-coding genes have been characterized in plant leaves, but little attention has been given to noncoding RNAs (ncRNAs). Moreover, increasing evidence indicates that an intricate interplay among RNA species, including protein-coding RNAs and ncRNAs, exists in eukaryotic transcriptomes, however, it remains elusive in plant leaves.ResultsWe detected novel ncRNAs, such as circular RNAs (circRNAs) and long noncoding RNAs (lncRNAs), and further constructed and analyzed their associated competitive endogenous RNA (ceRNA) networks in Arabidopsis leaves. Transcriptome profiling showed extensive changes during leaf development. In addition, comprehensive detection of circRNAs in other plant leaves suggested that circRNAs are widespread in plant leaves. To investigate the complex post-transcriptional interactions in Arabidopsis leaves, we constructed a global circRNA/lncRNA-associated...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4cd8r2tc</guid>
      <pubDate>Fri, 6 Sep 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Meng, Xianwen</name>
      </author>
      <author>
        <name>Zhang, Peijing</name>
      </author>
      <author>
        <name>Chen, Qi</name>
        <uri>https://orcid.org/0000-0001-6353-9589</uri>
      </author>
      <author>
        <name>Wang, Jingjing</name>
      </author>
      <author>
        <name>Chen, Ming</name>
      </author>
    </item>
    <item>
      <title>Adipocyte-Derived PXR Signaling Is Dispensable for Diet-Induced Obesity and Metabolic Disorders in Mice</title>
      <link>https://escholarship.org/uc/item/0xz656m2</link>
      <description>Pregnane X receptor (PXR) is a xenobiotic receptor that can be activated by numerous chemicals including endogenous hormones, dietary steroids, pharmaceutical agents, and environmental chemicals. PXR has been established to function as a xenobiotic sensor to coordinately regulate xenobiotic metabolism by regulating the expression of many enzymes and transporters required for xenobiotic metabolism. Recent studies have implicated a potentially important role for PXR in obesity and metabolic disease beyond xenobiotic metabolism, but how PXR action in different tissues or cell types contributes to obesity and metabolic disorders remains elusive. To investigate the role of adipocyte PXR in obesity, we generated a novel adipocyte-specific PXR deficient mouse model (PXR&lt;sup&gt;ΔAd&lt;/sup&gt;). Notably, we found that loss of adipocyte PXR did not affect food intake, energy expenditure, and obesity in high-fat diet-fed male mice. PXR&lt;sup&gt;ΔAd&lt;/sup&gt; mice also had similar obesity-associated metabolic...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0xz656m2</guid>
      <pubDate>Wed, 4 Sep 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Wang, Fang</name>
      </author>
      <author>
        <name>Liu, Jingwei</name>
      </author>
      <author>
        <name>Hernandez, Rebecca</name>
        <uri>https://orcid.org/0000-0002-8031-2949</uri>
      </author>
      <author>
        <name>Park, Se-Hyung</name>
      </author>
      <author>
        <name>Lai, Ying-Jing</name>
      </author>
      <author>
        <name>Wang, Shuxia</name>
      </author>
      <author>
        <name>Blumberg, Bruce</name>
        <uri>https://orcid.org/0000-0002-8016-8414</uri>
      </author>
      <author>
        <name>Zhou, Changcheng</name>
      </author>
    </item>
    <item>
      <title>Maternal n-3 enriched diet reprograms the offspring neurovascular transcriptome and blunts inflammation induced by endotoxin in the neonate</title>
      <link>https://escholarship.org/uc/item/1t82h5nd</link>
      <description>Infection during the perinatal period can adversely affect brain development, predispose infants to ischemic stroke and have lifelong consequences. We previously demonstrated that diet enriched in n-3 polyunsaturated fatty acids (n-3 PUFA) transforms brain lipid composition in the offspring and protects the neonatal brain from stroke, in part by blunting injurious immune responses. Critical to the interface between the brain and systemic circulation is the vasculature, endothelial cells in particular, that support brain homeostasis and provide a barrier to systemic infection. Here, we examined whether maternal PUFA-enriched diets exert reprograming of endothelial cell signalling in postnatal day 9 mice after modeling aspects of infection using LPS. Transcriptome analysis was performed on microvessels isolated from brains of pups from dams maintained on 3 different maternal diets from gestation day 1: standard, n-3 enriched or n-6 enriched diets. Depending on the diet, in endothelial...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1t82h5nd</guid>
      <pubDate>Mon, 2 Sep 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Chumak, Tetyana</name>
      </author>
      <author>
        <name>Jullienne, Amandine</name>
      </author>
      <author>
        <name>Ek, C Joakim</name>
      </author>
      <author>
        <name>Ardalan, Maryam</name>
      </author>
      <author>
        <name>Svedin, Pernilla</name>
      </author>
      <author>
        <name>Quan, Ryan</name>
      </author>
      <author>
        <name>Salehi, Arjang</name>
      </author>
      <author>
        <name>Salari, Sirus</name>
      </author>
      <author>
        <name>Obenaus, Andre</name>
        <uri>https://orcid.org/0000-0003-0081-6950</uri>
      </author>
      <author>
        <name>Vexler, Zinaida S</name>
      </author>
      <author>
        <name>Mallard, Carina</name>
      </author>
    </item>
    <item>
      <title>GRK2 kinases in the primary cilium initiate SMOOTHENED-PKA signaling in the Hedgehog cascade</title>
      <link>https://escholarship.org/uc/item/6kj3w439</link>
      <description>During Hedgehog (Hh) signal transduction in development and disease, the atypical G protein-coupled receptor (GPCR) SMOOTHENED (SMO) communicates with GLI transcription factors by binding the protein kinase A catalytic subunit (PKA-C) and physically blocking its enzymatic activity. Here, we show that GPCR kinase 2 (GRK2) orchestrates this process during endogenous mouse and zebrafish Hh pathway activation in the primary cilium. Upon SMO activation, GRK2 rapidly relocalizes from the ciliary base to the shaft, triggering SMO phosphorylation and PKA-C interaction. Reconstitution studies reveal that GRK2 phosphorylation enables active SMO to bind PKA-C directly. Lastly, the SMO-GRK2-PKA pathway underlies Hh signal transduction in a range of cellular and in vivo models. Thus, GRK2 phosphorylation of ciliary SMO and the ensuing PKA-C binding and inactivation are critical initiating events for the intracellular steps in Hh signaling. More broadly, our study suggests an expanded role...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6kj3w439</guid>
      <pubDate>Fri, 30 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Walker, Madison F</name>
      </author>
      <author>
        <name>Zhang, Jingyi</name>
      </author>
      <author>
        <name>Steiner, William</name>
      </author>
      <author>
        <name>Ku, Pei-I</name>
      </author>
      <author>
        <name>Zhu, Ju-Fen</name>
      </author>
      <author>
        <name>Michaelson, Zachary</name>
      </author>
      <author>
        <name>Yen, Yu-Chen</name>
      </author>
      <author>
        <name>Lee, Annabel</name>
      </author>
      <author>
        <name>Long, Alyssa B</name>
      </author>
      <author>
        <name>Casey, Mattie J</name>
      </author>
      <author>
        <name>Poddar, Abhishek</name>
      </author>
      <author>
        <name>Nelson, Isaac B</name>
      </author>
      <author>
        <name>Arveseth, Corvin D</name>
      </author>
      <author>
        <name>Nagel, Falko</name>
      </author>
      <author>
        <name>Clough, Ryan</name>
      </author>
      <author>
        <name>LaPotin, Sarah</name>
      </author>
      <author>
        <name>Kwan, Kristen M</name>
      </author>
      <author>
        <name>Schulz, Stefan</name>
      </author>
      <author>
        <name>Stewart, Rodney A</name>
      </author>
      <author>
        <name>Tesmer, John JG</name>
      </author>
      <author>
        <name>Caspary, Tamara</name>
      </author>
      <author>
        <name>Subramanian, Radhika</name>
      </author>
      <author>
        <name>Ge, Xuecai</name>
      </author>
      <author>
        <name>Myers, Benjamin R</name>
      </author>
    </item>
    <item>
      <title>Social deficits mirror delayed cerebrovascular dysfunction after traumatic brain injury</title>
      <link>https://escholarship.org/uc/item/7qm552wb</link>
      <description>Traumatic brain injury (TBI) survivors face debilitating long-term psychosocial consequences, including social isolation and depression. TBI modifies neurovascular physiology and behavior but the chronic physiological implications of altered brain perfusion on social interactions are unknown. Adult C57/BL6 male mice received a moderate cortical TBI, and social behaviors were assessed at baseline, 3-, 7-, 14-, 30-, and 60-days post injury (dpi). Magnetic resonance imaging (MRI, 9.4T) using dynamic susceptibility contrast perfusion weighted MRI were acquired. At 60dpi mice underwent histological angioarchitectural mapping. Analysis utilized standardized protocols followed by cross-correlation metrics. Social behavior deficits at 60dpi emerged as reduced interactions with a familiar cage-mate (partner) that mirrored significant reductions in cerebral blood flow (CBF) at 60dpi. CBF perturbations were dynamic temporally and across brain regions including regions known to regulate social...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7qm552wb</guid>
      <pubDate>Thu, 15 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Singh, Aditya</name>
      </author>
      <author>
        <name>Gong, Steven</name>
      </author>
      <author>
        <name>Vu, Anh</name>
      </author>
      <author>
        <name>Li, Scott</name>
      </author>
      <author>
        <name>Obenaus, Andre</name>
        <uri>https://orcid.org/0000-0003-0081-6950</uri>
      </author>
    </item>
    <item>
      <title>Toxoplasma infection induces an aged neutrophil population in the CNS that is associated with neuronal protection</title>
      <link>https://escholarship.org/uc/item/4m6534d7</link>
      <description>BackgroundInfection with the protozoan parasite Toxoplasma gondii leads to the formation of lifelong cysts in neurons that can have devastating consequences in the immunocompromised. In the immunocompetent individual, anti-parasitic effector mechanisms and a balanced immune response characterized by pro- and anti-inflammatory cytokine production establishes an asymptomatic infection that rarely leads to neurological symptoms. Several mechanisms are known to play a role in this successful immune response in the brain including T cell production of IFNγ and IL-10 and the involvement of CNS resident cells. This limitation of clinical neuropathology during chronic infection suggests a balance between immune response and neuroprotective mechanisms that collectively prevent clinical manifestations of disease. However, how these two vital mechanisms of protection interact during chronic Toxoplasma infection remains poorly understood.Main textThis study demonstrates a previously undescribed...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4m6534d7</guid>
      <pubDate>Mon, 12 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Bergersen, Kristina V</name>
      </author>
      <author>
        <name>Kavvathas, Bill</name>
      </author>
      <author>
        <name>Ford, Byron D</name>
      </author>
      <author>
        <name>Wilson, Emma H</name>
        <uri>https://orcid.org/0000-0002-6054-9981</uri>
      </author>
    </item>
    <item>
      <title>Human sperm RNA code senses dietary sugar</title>
      <link>https://escholarship.org/uc/item/7jw3j40m</link>
      <description>A new study reveals that a high-sugar diet acutely alters human sperm small RNA profiles after 1 week and that these changes are associated with changes in sperm motility. This rapid response by sperm to nutritional fluctuation raises intriguing questions regarding the underlying mechanisms and the potential effects on offspring metabolic health.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7jw3j40m</guid>
      <pubDate>Sun, 21 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Zhang, Ying</name>
      </author>
      <author>
        <name>Chen, Qi</name>
        <uri>https://orcid.org/0000-0001-6353-9589</uri>
      </author>
    </item>
    <item>
      <title>Adolescent exposure to low-dose THC disrupts energy balance and adipose organ homeostasis in adulthood</title>
      <link>https://escholarship.org/uc/item/1hg0j39v</link>
      <description>One of cannabis' most iconic effects is the stimulation of hedonic high-calorie eating-the "munchies"-yet habitual cannabis users are, on average, leaner than non-users. We asked whether this phenotype might result from lasting changes in energy balance established during adolescence, when use of the drug often begins. We found that daily low-dose administration of cannabis' intoxicating constituent, Δ&lt;sup&gt;9&lt;/sup&gt;-tetrahydrocannabinol (THC), to adolescent male mice causes an adult metabolic phenotype characterized by reduced fat mass, increased lean mass and utilization of fat as fuel, partial resistance to diet-induced obesity and dyslipidemia, enhanced thermogenesis, and impaired cold- and β-adrenergic receptor-stimulated lipolysis. Further analyses revealed that this phenotype is associated with molecular anomalies in the adipose organ, including ectopic overexpression of muscle-associated proteins and heightened anabolic processing. Thus, adolescent exposure to THC may promote...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1hg0j39v</guid>
      <pubDate>Sat, 20 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Lin, Lin</name>
      </author>
      <author>
        <name>Jung, Kwang-Mook</name>
      </author>
      <author>
        <name>Lee, Hye-Lim</name>
      </author>
      <author>
        <name>Le, Johnny</name>
      </author>
      <author>
        <name>Colleluori, Georgia</name>
      </author>
      <author>
        <name>Wood, Courtney</name>
      </author>
      <author>
        <name>Palese, Francesca</name>
      </author>
      <author>
        <name>Squire, Erica</name>
      </author>
      <author>
        <name>Ramirez, Jade</name>
      </author>
      <author>
        <name>Su, Shiqi</name>
      </author>
      <author>
        <name>Torrens, Alexa</name>
        <uri>https://orcid.org/0000-0001-7075-5669</uri>
      </author>
      <author>
        <name>Fotio, Yannick</name>
      </author>
      <author>
        <name>Tang, Lingyi</name>
      </author>
      <author>
        <name>Yu, Clinton</name>
      </author>
      <author>
        <name>Yang, Qin</name>
      </author>
      <author>
        <name>Huang, Lan</name>
        <uri>https://orcid.org/0000-0002-3140-4687</uri>
      </author>
      <author>
        <name>DiPatrizio, Nicholas</name>
        <uri>https://orcid.org/0000-0001-8423-0695</uri>
      </author>
      <author>
        <name>Jang, Cholsoon</name>
        <uri>https://orcid.org/0000-0002-4011-8164</uri>
      </author>
      <author>
        <name>Cinti, Saverio</name>
      </author>
      <author>
        <name>Piomelli, Daniele</name>
      </author>
    </item>
    <item>
      <title>Human neutrophil‐like cells demonstrate antimicrobial responses to the chronic cyst form of Toxoplasma gondii</title>
      <link>https://escholarship.org/uc/item/0n80f30k</link>
      <description>The protozoan parasite Toxoplasma gondii infects approximately 2.5 billion people worldwide. Infection induces a rapid dissemination of parasites throughout the body followed by the formation of lifelong cysts within neurons of the host brain. Both stages require a dynamic immune response comprised of both innate and adaptive cells. Neutrophils are a primary responding cell to acute infection and have been observed in the brain during murine chronic infection. Previous studies investigating human neutrophils found that invasion by Toxoplasma tachyzoites inhibits apoptosis of neutrophils, prolonging their survival under inflammatory conditions. Here, we demonstrate the differentiation of two distinct subsets following exposure of human neutrophil-like-cells (HNLC) to Toxoplasma cysts. In vitro stimulation and imaging studies show cyst-specific induction of cytokines and cyst clearance by HNLCs. Further testing demonstrates that aged HNLCs perform less phagocytosis of cysts compared...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0n80f30k</guid>
      <pubDate>Fri, 19 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Bergersen, Kristina V</name>
      </author>
      <author>
        <name>Ramirez, Ashley D</name>
      </author>
      <author>
        <name>Kavvathas, Bill</name>
      </author>
      <author>
        <name>Mercer, Frances</name>
      </author>
      <author>
        <name>Wilson, Emma H</name>
        <uri>https://orcid.org/0000-0002-6054-9981</uri>
      </author>
    </item>
    <item>
      <title>Spatiotemporal patterns of GFAP upregulation in rat brain following acute intoxication with diisopropylfluorophosphate (DFP).</title>
      <link>https://escholarship.org/uc/item/7kp4q8z9</link>
      <description>We previously demonstrated that the organophosphate diisopropylfluorophosphate (DFP) induced region-specific delayed neuronal injury in rat brain. The goal of this study was to examine the spatiotemporal pattern of the astroglial response after acute intoxication of rats with DFP. Rats were euthanized at varying times between 1 h to 7 days after DFP administration (9mg/kg, i.p.). The distribution of activated astrocytes in different brain regions was determined by immunostaining for glial fibrillary acidic acid (GFAP). GFAP immunoreactivity increased in the hippocampus, and piriform/entorhinal cortex at 1 h, peaked between 4-8 h then decreased from 16 to 24 h. GFAP labeling in the amygdala gradually increased over the 24 h period. A large increase in GFAP labeling was seen at 3-7 days following DFP administration in the hippocampus, piriform/entorhinal cortex and dorsolateral thalamus. At 3 days post-DFP exposure, GFAP immunoreactivity was totally absent in central areas of the...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7kp4q8z9</guid>
      <pubDate>Wed, 17 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Liu, Cuimei</name>
      </author>
      <author>
        <name>Li, Yonggang</name>
      </author>
      <author>
        <name>Lein, Pamela J</name>
        <uri>https://orcid.org/0000-0001-7665-7584</uri>
      </author>
      <author>
        <name>Ford, Byron D</name>
        <uri>https://orcid.org/0000-0002-6636-1461</uri>
      </author>
    </item>
    <item>
      <title>Neuregulin-1 is neuroprotective in a rat model of organophosphate-induced delayed neuronal injury</title>
      <link>https://escholarship.org/uc/item/3qx9q8h9</link>
      <description>Current medical countermeasures against organophosphate (OP) nerve agents are effective in reducing mortality, but do not sufficiently protect the CNS from delayed brain damage and persistent neurological symptoms. In this study, we examined the efficacy of neuregulin-1 (NRG-1) in protecting against delayed neuronal cell death following acute intoxication with the OP diisopropylflurophosphate (DFP). Adult male Sprague-Dawley rats were pretreated with pyridostigmine (0.1 mg/kg BW, i.m.) and atropine methylnitrate (20 mg/kg BW, i.m.) prior to DFP (9 mg/kg BW, i.p.) intoxication to increase survival and reduce peripheral signs of cholinergic toxicity but not prevent DFP-induced seizures or delayed neuronal injury. Pretreatment with NRG-1 did not protect against seizures in rats exposed to DFP. However, neuronal injury was significantly reduced in most brain regions by pretreatment with NRG-1 isoforms NRG-EGF (3.2 μg/kg BW, i.a) or NRG-GGF2 (48 μg/kg BW, i.a.) as determined by FluroJade-B...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3qx9q8h9</guid>
      <pubDate>Wed, 17 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Li, Yonggang</name>
      </author>
      <author>
        <name>Lein, Pamela J</name>
        <uri>https://orcid.org/0000-0001-7665-7584</uri>
      </author>
      <author>
        <name>Liu, Cuimei</name>
      </author>
      <author>
        <name>Bruun, Donald A</name>
      </author>
      <author>
        <name>Giulivi, Cecilia</name>
        <uri>https://orcid.org/0000-0003-1033-7435</uri>
      </author>
      <author>
        <name>Ford, Gregory D</name>
      </author>
      <author>
        <name>Tewolde, Teclemichael</name>
      </author>
      <author>
        <name>Ross-Inta, Catherine</name>
      </author>
      <author>
        <name>Ford, Byron D</name>
        <uri>https://orcid.org/0000-0002-6636-1461</uri>
      </author>
    </item>
    <item>
      <title>Deciphering Abnormal Platelet Subpopulations in COVID-19, Sepsis and Systemic Lupus Erythematosus through Machine Learning and Single-Cell Transcriptomics</title>
      <link>https://escholarship.org/uc/item/49m3q0cd</link>
      <description>This study focuses on understanding the transcriptional heterogeneity of activated platelets and its impact on diseases such as sepsis, COVID-19, and systemic lupus erythematosus (SLE). Recognizing the limited knowledge in this area, our research aims to dissect the complex transcriptional profiles of activated platelets to aid in developing targeted therapies for abnormal and pathogenic platelet subtypes. We analyzed single-cell transcriptional profiles from 47,977 platelets derived from 413 samples of patients with these diseases, utilizing Deep Neural Network (DNN) and eXtreme Gradient Boosting (XGB) to distinguish transcriptomic signatures predictive of fatal or survival outcomes. Our approach included source data annotations and platelet markers, along with SingleR and Seurat for comprehensive profiling. Additionally, we employed Uniform Manifold Approximation and Projection (UMAP) for effective dimensionality reduction and visualization, aiding in the identification of various...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/49m3q0cd</guid>
      <pubDate>Sat, 6 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Qiu, Xinru</name>
      </author>
      <author>
        <name>Nair, Meera G</name>
        <uri>https://orcid.org/0000-0002-1807-5161</uri>
      </author>
      <author>
        <name>Jaroszewski, Lukasz</name>
      </author>
      <author>
        <name>Godzik, Adam</name>
      </author>
    </item>
    <item>
      <title>Interferon-β deficiency alters brain response to chronic HIV-1 envelope protein exposure in a transgenic model of NeuroHIV</title>
      <link>https://escholarship.org/uc/item/4581t0pv</link>
      <description>Human immunodeficiency virus-1 (HIV-1) infects the central nervous system (CNS) and causes HIV-associated neurocognitive disorders (HAND) in about half of the population living with the virus despite combination anti-retroviral therapy (cART). HIV-1 activates the innate immune system, including the production of type 1 interferons (IFNs) α and β. Transgenic mice expressing HIV-1 envelope glycoprotein gp120 (HIVgp120tg) in the CNS develop memory impairment and share key neuropathological features and differential CNS gene expression with HIV patients, including the induction of IFN-stimulated genes (ISG). Here we show that knocking out IFNβ (IFNβKO) in HIVgp120tg and non-tg control mice impairs recognition and spatial memory, but does not affect anxiety-like behavior, locomotion, or vision. The neuropathology of HIVgp120tg mice is only moderately affected by the KO of IFNβ but in a sex-dependent fashion. Notably, in cerebral cortex of IFNβKO animals presynaptic terminals are reduced...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4581t0pv</guid>
      <pubDate>Sat, 29 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Singh, Hina</name>
        <uri>https://orcid.org/0000-0001-7067-1991</uri>
      </author>
      <author>
        <name>Koury, Jeffrey</name>
      </author>
      <author>
        <name>Maung, Ricky</name>
      </author>
      <author>
        <name>Roberts, Amanda J</name>
      </author>
      <author>
        <name>Kaul, Marcus</name>
      </author>
    </item>
    <item>
      <title>Stable Occupancy of the Crimean-Congo Hemorrhagic Fever Virus-Encoded Deubiquitinase Blocks Viral Infection</title>
      <link>https://escholarship.org/uc/item/9fq1j0tm</link>
      <description>Crimean-Congo hemorrhagic fever virus (CCHFV) infection can result in a severe hemorrhagic syndrome for which there are no antiviral interventions available to date. Certain RNA viruses, such as CCHFV, encode cysteine proteases of the ovarian tumor (OTU) family that antagonize interferon (IFN) production by deconjugating ubiquitin (Ub). The OTU of CCHFV, a negative-strand RNA virus, is dispensable for replication of the viral genome, despite being part of the large viral RNA polymerase. Here, we show that mutations that prevent binding of the OTU to cellular ubiquitin are required for the generation of recombinant CCHFV containing a mutated catalytic cysteine. Similarly, the high-affinity binding of a synthetic ubiquitin variant (UbV-CC4) to CCHFV OTU strongly inhibits viral growth. UbV-CC4 inhibits CCHFV infection even in the absence of intact IFN signaling, suggesting that its antiviral activity is not due to blocking the OTU's immunosuppressive function. Instead, the prolonged...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9fq1j0tm</guid>
      <pubDate>Mon, 24 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Scholte, Florine EM</name>
      </author>
      <author>
        <name>Hua, Brian L</name>
      </author>
      <author>
        <name>Spengler, Jessica R</name>
      </author>
      <author>
        <name>Dzimianski, John V</name>
      </author>
      <author>
        <name>Coleman-McCray, JoAnn D</name>
      </author>
      <author>
        <name>Welch, Stephen R</name>
      </author>
      <author>
        <name>McMullan, Laura K</name>
      </author>
      <author>
        <name>Nichol, Stuart T</name>
      </author>
      <author>
        <name>Pegan, Scott D</name>
        <uri>https://orcid.org/0000-0002-2958-5319</uri>
      </author>
      <author>
        <name>Spiropoulou, Christina F</name>
      </author>
      <author>
        <name>Bergeron, Éric</name>
      </author>
    </item>
    <item>
      <title>Structural Insights into the Interaction of Coronavirus Papain-Like Proteases and Interferon-Stimulated Gene Product 15 from Different Species</title>
      <link>https://escholarship.org/uc/item/7dm1218m</link>
      <description>Severe acute respiratory syndrome coronavirus (SARS-CoV) and Middle East respiratory syndrome coronavirus (MERS-CoV) encode multifunctional papain-like proteases (PLPs) that have the ability to process the viral polyprotein to facilitate RNA replication and antagonize the host innate immune response. The latter function involves reversing the post-translational modification of cellular proteins conjugated with either ubiquitin (Ub) or Ub-like interferon-stimulated gene product 15 (ISG15). Ub is known to be highly conserved among eukaryotes, but surprisingly, ISG15 is highly divergent among animals. The ramifications of this sequence divergence to the recognition of ISG15 by coronavirus PLPs at a structural and biochemical level are poorly understood. Therefore, the activity of PLPs from SARS-CoV, MERS-CoV, and mouse hepatitis virus was evaluated against seven ISG15s originating from an assortment of animal species susceptible, and not, to certain coronavirus infections. Excitingly,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7dm1218m</guid>
      <pubDate>Mon, 24 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Daczkowski, Courtney M</name>
      </author>
      <author>
        <name>Dzimianski, John V</name>
      </author>
      <author>
        <name>Clasman, Jozlyn R</name>
      </author>
      <author>
        <name>Goodwin, Octavia</name>
      </author>
      <author>
        <name>Mesecar, Andrew D</name>
      </author>
      <author>
        <name>Pegan, Scott D</name>
        <uri>https://orcid.org/0000-0002-2958-5319</uri>
      </author>
    </item>
    <item>
      <title>Structural insights into the interaction of papain-like protease 2 from the alphacoronavirus porcine epidemic diarrhea virus and ubiquitin</title>
      <link>https://escholarship.org/uc/item/6g51671w</link>
      <description>Porcine epidemic diarrhea is a devastating porcine disease that is caused by the alphacoronavirus porcine epidemic diarrhea virus (PEDV). Like other members of the Coronaviridae family, PEDV encodes a multifunctional papain-like protease 2 (PLP2) that has the ability to process the coronavirus viral polyprotein to aid in RNA replication and antagonize the host innate immune response through cleavage of the regulatory proteins ubiquitin (Ub) and/or interferon-stimulated gene product 15 (ISG15) (deubiquitination and deISGylation, respectively). Because Betacoronavirus PLPs have been well characterized, it was sought to determine how PLP2 from the alphacoronavirus PEDV differentiates itself from its related counterparts. PEDV PLP2 was first biochemically characterized, and a 3.1 Å resolution crystal structure of PEDV PLP2 bound to Ub was then solved, providing insight into how Alphacoronavirus PLPs bind to their preferred substrate, Ub. It was found that PEDV PLP2 is a deubiquitinase...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6g51671w</guid>
      <pubDate>Mon, 24 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Durie, Ian A</name>
      </author>
      <author>
        <name>Dzimianski, John V</name>
      </author>
      <author>
        <name>Daczkowski, Courtney M</name>
      </author>
      <author>
        <name>McGuire, Jack</name>
      </author>
      <author>
        <name>Faaberg, Kay</name>
      </author>
      <author>
        <name>Pegan, Scott D</name>
        <uri>https://orcid.org/0000-0002-2958-5319</uri>
      </author>
    </item>
    <item>
      <title>Crimean-Congo Hemorrhagic Fever Virus Suppresses Innate Immune Responses via a Ubiquitin and ISG15 Specific Protease</title>
      <link>https://escholarship.org/uc/item/4ps924mj</link>
      <description>Antiviral responses are regulated by conjugation of ubiquitin (Ub) and interferon-stimulated gene 15 (ISG15) to proteins. Certain classes of viruses encode Ub- or ISG15-specific proteases belonging to the ovarian tumor (OTU) superfamily. Their activity is thought to suppress cellular immune responses, but studies demonstrating the function of viral OTU proteases during infection are lacking. Crimean-Congo hemorrhagic fever virus (CCHFV, family Nairoviridae) is a highly pathogenic human virus that encodes an OTU with both deubiquitinase and deISGylase activity as part of the viral RNA polymerase. We investigated CCHFV OTU function by inactivating protease catalytic activity or by selectively disrupting its deubiquitinase and deISGylase activity using reverse genetics. CCHFV OTU inactivation blocked viral replication independently of its RNA polymerase activity, while deubiquitinase activity proved critical for suppressing the interferon responses. Our findings provide insights...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4ps924mj</guid>
      <pubDate>Mon, 24 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Scholte, Florine EM</name>
      </author>
      <author>
        <name>Zivcec, Marko</name>
      </author>
      <author>
        <name>Dzimianski, John V</name>
      </author>
      <author>
        <name>Deaton, Michelle K</name>
      </author>
      <author>
        <name>Spengler, Jessica R</name>
      </author>
      <author>
        <name>Welch, Stephen R</name>
      </author>
      <author>
        <name>Nichol, Stuart T</name>
      </author>
      <author>
        <name>Pegan, Scott D</name>
        <uri>https://orcid.org/0000-0002-2958-5319</uri>
      </author>
      <author>
        <name>Spiropoulou, Christina F</name>
      </author>
      <author>
        <name>Bergeron, Éric</name>
      </author>
    </item>
    <item>
      <title>ISG15: It's Complicated</title>
      <link>https://escholarship.org/uc/item/40z020m1</link>
      <description>Interferon-stimulated gene product 15 (ISG15) is a key component of host responses to microbial infection. Despite having been known for four decades, grasping the functions and features of ISG15 has been a slow and elusive process. Substantial work over the past two decades has greatly enhanced this understanding, revealing the complex and variable nature of this protein. This has unveiled multiple mechanisms of action that are only now beginning to be understood. In addition, it has uncovered diversity not only between how ISG15 affects different pathogens but also between the function and structure of ISG15 itself between different host species. Here we review the complexity of ISG15 within the context of viral infection, focusing primarily on its antiviral function and the mechanisms viruses employ to thwart its effects. We highlight what is known regarding the impact of ISG15 sequence and structural diversity on these interactions and discuss the aspects presenting the next...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/40z020m1</guid>
      <pubDate>Mon, 24 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Dzimianski, John V</name>
      </author>
      <author>
        <name>Scholte, Florine EM</name>
      </author>
      <author>
        <name>Bergeron, Éric</name>
      </author>
      <author>
        <name>Pegan, Scott D</name>
        <uri>https://orcid.org/0000-0002-2958-5319</uri>
      </author>
    </item>
    <item>
      <title>Probing the impact of nairovirus genomic diversity on viral ovarian tumor domain protease (vOTU) structure and deubiquitinase activity</title>
      <link>https://escholarship.org/uc/item/3pn1v36m</link>
      <description>Post-translational modification of host and viral proteins by ubiquitin (Ub) and Ub-like proteins, such as interferon stimulated gene product 15 (ISG15), plays a key role in response to infection. Viruses have been increasingly identified that contain proteases possessing deubiquitinase (DUB) and/or deISGylase functions. This includes viruses in the Nairoviridae family that encode a viral homologue of the ovarian tumor protease (vOTU). vOTU activity was recently demonstrated to be critical for replication of the often-fatal Crimean-Congo hemorrhagic fever virus, with DUB activity suppressing the type I interferon responses and deISGylase activity broadly removing ISG15 conjugated proteins. There are currently about 40 known nairoviruses classified into fourteen species. Recent genomic characterization has revealed a high degree of diversity, with vOTUs showing less than 25% amino acids identities within the family. Previous investigations have been limited to only a few closely...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3pn1v36m</guid>
      <pubDate>Mon, 24 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Dzimianski, John V</name>
      </author>
      <author>
        <name>Beldon, Brianna S</name>
      </author>
      <author>
        <name>Daczkowski, Courtney M</name>
      </author>
      <author>
        <name>Goodwin, Octavia Y</name>
      </author>
      <author>
        <name>Scholte, Florine EM</name>
      </author>
      <author>
        <name>Bergeron, Éric</name>
      </author>
      <author>
        <name>Pegan, Scott D</name>
        <uri>https://orcid.org/0000-0002-2958-5319</uri>
      </author>
    </item>
    <item>
      <title>Determining the molecular drivers of species-specific interferon-stimulated gene product 15 interactions with nairovirus ovarian tumor domain proteases</title>
      <link>https://escholarship.org/uc/item/3hf896hb</link>
      <description>Tick-borne nairoviruses (order Bunyavirales) encode an ovarian tumor domain protease (OTU) that suppresses the innate immune response by reversing the post-translational modification of proteins by ubiquitin (Ub) and interferon-stimulated gene product 15 (ISG15). Ub is highly conserved across eukaryotes, whereas ISG15 is only present in vertebrates and shows substantial sequence diversity. Prior attempts to address the effect of ISG15 diversity on viral protein-ISG15 interactions have focused on only a single species' ISG15 or a limited selection of nairovirus OTUs. To gain a more complete perspective of OTU-ISG15 interactions, we biochemically assessed the relative activities of 14 diverse nairovirus OTUs for 12 species' ISG15 and found that ISG15 activity is predominantly restricted to particular nairovirus lineages reflecting, in general, known virus-host associations. To uncover the underlying molecular factors driving OTUs affinity for ISG15, X-ray crystal structures of Kupe...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3hf896hb</guid>
      <pubDate>Mon, 24 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Dzimianski, John V</name>
      </author>
      <author>
        <name>Scholte, Florine EM</name>
      </author>
      <author>
        <name>Williams, Isabelle L</name>
      </author>
      <author>
        <name>Langley, Caroline</name>
      </author>
      <author>
        <name>Freitas, Brendan T</name>
      </author>
      <author>
        <name>Spengler, Jessica R</name>
      </author>
      <author>
        <name>Bergeron, Éric</name>
      </author>
      <author>
        <name>Pegan, Scott D</name>
        <uri>https://orcid.org/0000-0002-2958-5319</uri>
      </author>
    </item>
    <item>
      <title>Structure of interferon-stimulated gene product 15 (ISG15) from the bat species Myotis davidii and the impact of interdomain ISG15 interactions on viral protein engagement</title>
      <link>https://escholarship.org/uc/item/2n93x18v</link>
      <description>Bats have long been observed to be the hosts and the origin of numerous human diseases. Bats, like all mammals, rely on a number of innate immune mechanisms to combat invading pathogens, including the interferon type I, II and III responses. Ubiquitin-like interferon-stimulated gene product 15 (ISG15) is a key modulator of these interferon responses. Within these pathways, ISG15 can serve to stabilize host proteins modulating innate immune responses and act as a cytokine. Post-translational modifications of viral proteins introduced by ISG15 have also been observed to directly affect the function of numerous viral proteins. Unlike ubiquitin, which is virtually identical across all animals, comparison of ISG15s across species reveals that they are relatively divergent, with sequence identity dropping to as low as ∼58% among mammals. In addition to serving as an obstacle to the zoonotic transmission of influenza, these ISG15 species-species differences have also long been shown...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2n93x18v</guid>
      <pubDate>Mon, 24 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Langley, Caroline</name>
      </author>
      <author>
        <name>Goodwin, Octavia</name>
      </author>
      <author>
        <name>Dzimianski, John V</name>
      </author>
      <author>
        <name>Daczkowski, Courtney M</name>
      </author>
      <author>
        <name>Pegan, Scott D</name>
        <uri>https://orcid.org/0000-0002-2958-5319</uri>
      </author>
    </item>
    <item>
      <title>Biochemical and Structural Insights into the Preference of Nairoviral DeISGylases for Interferon-Stimulated Gene Product 15 Originating from Certain Species</title>
      <link>https://escholarship.org/uc/item/1j92r0md</link>
      <description>The regulation of the interferon type I (IFN-I) response has been shown to rely on posttranslational modification by ubiquitin (Ub) and Ub-like interferon-stimulated gene product 15 (ISG15) to stabilize, or activate, a variety of IFN-I signaling and downstream effector proteins. Unlike Ub, which is almost perfectly conserved among eukaryotes, ISG15 is highly divergent, even among mammals. Since zoonotic viruses rely on viral proteins to recognize, or cleave, ISG15 conjugates in order to evade, or suppress, innate immunity, the impact of ISG15 biodiversity on deISGylating proteases of the ovarian tumor family (vOTU) from nairoviruses was evaluated. The enzymatic activities of vOTUs originating from the Crimean-Congo hemorrhagic fever virus, Erve virus, and Nairobi sheep disease virus were tested against ISG15s from humans, mice, shrews, sheep, bats, and camels, which are mammalian species known to be infected by nairoviruses. This along with investigation of binding by isothermal...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1j92r0md</guid>
      <pubDate>Mon, 24 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Deaton, MK</name>
      </author>
      <author>
        <name>Dzimianski, JV</name>
      </author>
      <author>
        <name>Daczkowski, CM</name>
      </author>
      <author>
        <name>Whitney, GK</name>
      </author>
      <author>
        <name>Mank, NJ</name>
      </author>
      <author>
        <name>Parham, MM</name>
      </author>
      <author>
        <name>Bergeron, E</name>
      </author>
      <author>
        <name>Pegan, SD</name>
        <uri>https://orcid.org/0000-0002-2958-5319</uri>
      </author>
    </item>
    <item>
      <title>A Novel, Noninvasive, Predictive Epilepsy Biomarker with Clinical Potential</title>
      <link>https://escholarship.org/uc/item/8kq1x8hm</link>
      <description>A significant proportion of temporal lobe epilepsy (TLE), a common, intractable brain disorder, arises in children with febrile status epilepticus (FSE). Preventative therapy development is hampered by our inability to identify early the FSE individuals who will develop TLE. In a naturalistic rat model of FSE, we used high-magnetic-field MRI and long-term video EEG to seek clinically relevant noninvasive markers of epileptogenesis and found that reduced amygdala T2 relaxation times in high-magnetic-field MRI hours after FSE predicted experimental TLE. Reduced T2 values likely represented paramagnetic susceptibility effects derived from increased unsaturated venous hemoglobin, suggesting augmented oxygen utilization after FSE termination. Indeed, T2 correlated with energy-demanding intracellular translocation of the injury-sensor high-mobility group box 1 (HMGB1), a trigger of inflammatory cascades implicated in epileptogenesis. Use of deoxyhemoglobin-sensitive MRI sequences enabled...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8kq1x8hm</guid>
      <pubDate>Mon, 17 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Choy, ManKin</name>
      </author>
      <author>
        <name>Dubé, Celine M</name>
      </author>
      <author>
        <name>Patterson, Katelin</name>
      </author>
      <author>
        <name>Barnes, Samuel R</name>
      </author>
      <author>
        <name>Maras, Pamela</name>
      </author>
      <author>
        <name>Blood, Arlin B</name>
      </author>
      <author>
        <name>Hasso, Anton N</name>
      </author>
      <author>
        <name>Obenaus, Andre</name>
        <uri>https://orcid.org/0000-0003-0081-6950</uri>
      </author>
      <author>
        <name>Baram, Tallie Z</name>
        <uri>https://orcid.org/0000-0003-0771-8616</uri>
      </author>
    </item>
    <item>
      <title>Intravital Multiphoton Examination of Implant-Associated Staphylococcus aureus Biofilm Infection</title>
      <link>https://escholarship.org/uc/item/7wz458w3</link>
      <description>Bacterial infections associated with implanted medical devices represents a healthcare crisis due to their persistence, antibiotic tolerance, and immune avoidance. Indwelling devices are rapidly coated with host plasma and extracellular matrix proteins which can then be exploited by bacterial pathogens for adherence and subsequent biofilm development. Our understanding of the host-pathogen interface that determines the fate of biofilm-mediated infections is limited to the experimental models employed by laboratories studying these organisms. Current &lt;i&gt;in vivo&lt;/i&gt; models of biofilm-mediated infection, while certainly useful, are typically limited to end-point analyses of bacterial burden enumeration, immune cell profiling, and cytokine/chemokine analysis. Thus, with these models, the complex, real-time assessment of biofilm development and innate immune cell activity remains imperceptible. Here, we describe a novel murine biofilm infection model employing time-lapse intravital...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7wz458w3</guid>
      <pubDate>Mon, 27 May 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Gries, Casey M</name>
      </author>
      <author>
        <name>Rivas, Zuivanna</name>
      </author>
      <author>
        <name>Chen, Justin</name>
      </author>
      <author>
        <name>Lo, David D</name>
        <uri>https://orcid.org/0000-0002-5962-9458</uri>
      </author>
    </item>
    <item>
      <title>Novel Mechanical Strain Characterization of Ventilated ex vivo Porcine and Murine Lung using Digital Image Correlation</title>
      <link>https://escholarship.org/uc/item/7bk49651</link>
      <description>Respiratory illnesses, such as bronchitis, emphysema, asthma, and COVID-19, substantially remodel lung tissue, deteriorate function, and culminate in a compromised breathing ability. Yet, the structural mechanics of the lung is significantly understudied. Classical pressure-volume air or saline inflation studies of the lung have attempted to characterize the organ's elasticity and compliance, measuring deviatory responses in diseased states; however, these investigations are exclusively limited to the bulk composite or global response of the entire lung and disregard local expansion and stretch phenomena within the lung lobes, overlooking potentially valuable physiological insights, as particularly related to mechanical ventilation. Here, we present a method to collect the first non-contact, full-field deformation measures of &lt;i&gt;ex vivo&lt;/i&gt; porcine and murine lungs and interface with a pressure-volume ventilation system to investigate lung behavior in real time. We share preliminary...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7bk49651</guid>
      <pubDate>Mon, 27 May 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Mariano, Crystal A</name>
      </author>
      <author>
        <name>Sattari, Samaneh</name>
      </author>
      <author>
        <name>Maghsoudi-Ganjeh, Mohammad</name>
      </author>
      <author>
        <name>Tartibi, Mehrzad</name>
      </author>
      <author>
        <name>Lo, David D</name>
        <uri>https://orcid.org/0000-0002-5962-9458</uri>
      </author>
      <author>
        <name>Eskandari, Mona</name>
      </author>
    </item>
    <item>
      <title>CD137 signaling enhances tight junction resistance in intestinal epithelial cells</title>
      <link>https://escholarship.org/uc/item/6618w281</link>
      <description>Treatment of Caco-2-BBe intestinal epithelial cells (BBe) with TNF-α and lymphotoxin-β (LT-β) receptor agonists induced the expression of the TNF receptor superfamily gene TNFRSF9/CD137. In the gut, these cytokines are known to be involved in both inflammatory responses and development of organized lymphoid tissues; thus, it was notable that in CD137-deficient mice Peyer's patch M cells lacked transcytosis function. To examine the direct effect of CD137 expression on epithelial cell function independent of other cytokine effects including CD137L triggering, we stably transfected BBe cells to express CD137. CD137 was found at the cell surface as well as the cytoplasm, and confocal microscopy suggested that aggregates of CD137 at the lateral and basolateral surface may be associated with cytoplasmic actin filament termini. Many of the CD137 clusters were colocalized with extracellular fibronectin providing a possible alternative ligand for CD137. Interestingly, we found that CD137-expressing...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6618w281</guid>
      <pubDate>Mon, 27 May 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Gusti, Veronica</name>
      </author>
      <author>
        <name>Bennett, Kaila M</name>
      </author>
      <author>
        <name>Lo, David D</name>
        <uri>https://orcid.org/0000-0002-5962-9458</uri>
      </author>
    </item>
    <item>
      <title>Inducible Colonic M Cells Are Dependent on TNFR2 but Not Ltβr, Identifying Distinct Signalling Requirements for Constitutive Versus Inducible M Cells</title>
      <link>https://escholarship.org/uc/item/5d2532ct</link>
      <description>BACKGROUND AND AIMS: M cells associated with organised lymphoid tissues such as intestinal Peyer's patches provide surveillance of the intestinal lumen. Inflammation or infection in the colon can induce an M cell population associated with lymphoid infiltrates; paradoxically, induction is dependent on the inflammatory cytokine tumour necrosis factor [TNF]-α. Anti-TNFα blockade is an important therapeutic in inflammatory bowel disease, so understanding the effects of TNFα signalling is important in refining therapeutics.
METHODS: To dissect pro-inflammatory signals from M cell inductive signals, we used confocal microscopy image analysis to assess requirements for specific cytokine receptor signals using TNF receptor 1 [TNFR1] and 2 [TNFR2] knockouts [ko] back-crossed to the PGRP-S-dsRed transgene; separate groups were treated with soluble lymphotoxin β receptor [sLTβR] to block LTβR signalling. All groups were treated with dextran sodium sulphate [DSS] to induce colitis.
RESULTS:...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5d2532ct</guid>
      <pubDate>Mon, 27 May 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Parnell, Erinn A</name>
      </author>
      <author>
        <name>Walch, Erin M</name>
      </author>
      <author>
        <name>Lo, David D</name>
        <uri>https://orcid.org/0000-0002-5962-9458</uri>
      </author>
    </item>
    <item>
      <title>Staphylococcus aureus Fibronectin Binding Protein A Mediates Biofilm Development and Infection</title>
      <link>https://escholarship.org/uc/item/5992q7gz</link>
      <description>Implanted medical device-associated infections pose significant health risks, as they are often the result of bacterial biofilm formation. &lt;i&gt;Staphylococcus aureus&lt;/i&gt; is a leading cause of biofilm-associated infections which persist due to mechanisms of device surface adhesion, biofilm accumulation, and reprogramming of host innate immune responses. We found that the &lt;i&gt;S. aureus&lt;/i&gt; fibronectin binding protein A (FnBPA) is required for normal biofilm development in mammalian serum and that the SaeRS two-component system is required for functional FnBPA activity in serum. Furthermore, serum-developed biofilms deficient in FnBPA were more susceptible to macrophage invasion, and in a model of biofilm-associated implant infection, we found that FnBPA is crucial for the establishment of infection. Together, these findings show that &lt;i&gt;S. aureus&lt;/i&gt; FnBPA plays an important role in physical biofilm development and represents a potential therapeutic target for the prevention and treatment...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5992q7gz</guid>
      <pubDate>Mon, 27 May 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Gries, Casey M</name>
      </author>
      <author>
        <name>Biddle, Trevor</name>
      </author>
      <author>
        <name>Bose, Jeffrey L</name>
      </author>
      <author>
        <name>Kielian, Tammy</name>
      </author>
      <author>
        <name>Lo, David D</name>
        <uri>https://orcid.org/0000-0002-5962-9458</uri>
      </author>
    </item>
    <item>
      <title>M Cells: Intelligent Engineering of Mucosal Immune Surveillance</title>
      <link>https://escholarship.org/uc/item/2tm8t51t</link>
      <description>M cells are specialized intestinal epithelial cells that provide the main machinery for sampling luminal microbes for mucosal immune surveillance. M cells are usually found in the epithelium overlying organized mucosal lymphoid tissues, but studies have identified multiple distinct lineages of M cells that are produced under different conditions, including intestinal inflammation. Among these lineages there is a common morphology that helps explain the efficiency of M cells in capturing luminal bacteria and viruses; in addition, M cells recruit novel cellular mechanisms to transport the particles across the mucosal barrier into the lamina propria, a process known as transcytosis. These specializations used by M cells point to a novel engineering of cellular machinery to selectively capture and transport microbial particles of interest. Because of the ability of M cells to effectively violate the mucosal barrier, the circumstances of M cell induction have important consequences....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2tm8t51t</guid>
      <pubDate>Mon, 27 May 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Dillon, Andrea</name>
      </author>
      <author>
        <name>Lo, David D</name>
        <uri>https://orcid.org/0000-0002-5962-9458</uri>
      </author>
    </item>
    <item>
      <title>Route of administration significantly affects particle deposition and cellular recruitment</title>
      <link>https://escholarship.org/uc/item/18r9h332</link>
      <description>Lung exposures to dusts, pollutants, and other aerosol particulates are known to be associated with pulmonary diseases such as asthma and Chronic Obstructive Pulmonary Disease. These health impacts are attributed to the ability of aerosol components to induce pulmonary inflammation, which promotes tissue remodeling, including fibrosis, tissue degradation, and smooth muscle proliferation. Consequently, the distribution of these effects can have a significant impact on the physiologic function of the lung. In order to study the impact of distribution of inhaled particulates on lung pathogenesis, we compared the effect of different methods of particle delivery. By comparing intranasal versus aerosol delivery of fluorescent microspheres, we observed strikingly distinct patterns of particle deposition; intranasal delivery provided focused deposition concentrated on larger airways, while aerosol delivery showed unform deposition throughout the lung parenchyma. Recognizing that the impacts...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/18r9h332</guid>
      <pubDate>Mon, 27 May 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Yisrael, Keziyah</name>
      </author>
      <author>
        <name>Drover, Ryan W</name>
      </author>
      <author>
        <name>Shapiro, Malia L</name>
      </author>
      <author>
        <name>Anguiano, Martha</name>
      </author>
      <author>
        <name>Kachour, Nala</name>
      </author>
      <author>
        <name>Li, Qi</name>
      </author>
      <author>
        <name>Tran, Emily</name>
      </author>
      <author>
        <name>Cocker, David R</name>
      </author>
      <author>
        <name>Lo, David D</name>
        <uri>https://orcid.org/0000-0002-5962-9458</uri>
      </author>
    </item>
    <item>
      <title>Selective Targeting of Tumour Necrosis Factor Receptor 1 Induces Stable Protection from Crohn’s-Like Ileitis in TNFΔARE Mice</title>
      <link>https://escholarship.org/uc/item/0gd0015n</link>
      <description>BACKGROUND AND AIMS: Crohn's disease is a debilitating chronic inflammatory disorder of the mammalian gastrointestinal tract. Current interventions using anti-tumour necrosis factor [anti-TNF] biologics show long-term benefit in only half of patients. This study focused on the role of the TNF receptor 1 [TNFR1] in pathogenesis in a TNF-driven model of ileitis.
METHODS: We studied TNFΔAU-rich element [ARE]/+ [TNFdARE] mice, which develop progressive ileitis similar to Crohn's ileitis. Histopathological analysis and gene expression profiling were used to characterize disease progression from 5 to 16 weeks. Mice with TNFR1 hemizygosity [TNFdARE/R1het] allowed us to assess gene dosage effects. Transcriptional profiling established inflection points in disease progression; inflammatory gene expression increased at 8 weeks with a plateau by 10 weeks, so these were selected as endpoints of treatment using the TNF biologic infliximab and the TNFR1-specific XPro1595. Differences in recruitment...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0gd0015n</guid>
      <pubDate>Mon, 27 May 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Chakraborty, Rajrupa</name>
      </author>
      <author>
        <name>Maltz, Mia R</name>
      </author>
      <author>
        <name>Del Castillo, Diana</name>
      </author>
      <author>
        <name>Tandel, Purvi N</name>
      </author>
      <author>
        <name>Messih, Nathalie</name>
      </author>
      <author>
        <name>Anguiano, Martha</name>
      </author>
      <author>
        <name>Lo, David D</name>
        <uri>https://orcid.org/0000-0002-5962-9458</uri>
      </author>
    </item>
    <item>
      <title>Epistatic interactions between NMD and TRP53 control progenitor cell maintenance and brain size</title>
      <link>https://escholarship.org/uc/item/9742k8ch</link>
      <description>Mutations in human nonsense-mediated mRNA decay (NMD) factors are enriched in neurodevelopmental disorders. We show that deletion of key NMD factor Upf2 in mouse embryonic neural progenitor cells causes perinatal microcephaly but deletion in immature neurons does not, indicating NMD's critical roles in progenitors. Upf2 knockout (KO) prolongs the cell cycle of radial glia progenitor cells, promotes their transition into intermediate progenitors, and leads to reduced upper-layer neurons. CRISPRi screening identified Trp53 knockdown rescuing Upf2KO progenitors without globally reversing NMD inhibition, implying marginal contributions&amp;nbsp;of most NMD targets to the cell cycle defect. Integrated functional genomics shows that NMD degrades selective TRP53 downstream targets, including Cdkn1a, which, without NMD suppression, slow the cell cycle. Trp53KO restores the progenitor cell pool and rescues the microcephaly of Upf2KO mice. Therefore, one physiological role of NMD in the developing...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9742k8ch</guid>
      <pubDate>Thu, 23 May 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Lin, Lin</name>
      </author>
      <author>
        <name>Zhao, Jingrong</name>
      </author>
      <author>
        <name>Kubota, Naoto</name>
        <uri>https://orcid.org/0000-0003-0612-2300</uri>
      </author>
      <author>
        <name>Li, Zhelin</name>
      </author>
      <author>
        <name>Lam, Yi-Li</name>
      </author>
      <author>
        <name>Nguyen, Lauren P</name>
      </author>
      <author>
        <name>Yang, Lu</name>
      </author>
      <author>
        <name>Pokharel, Sheela P</name>
      </author>
      <author>
        <name>Blue, Steven M</name>
      </author>
      <author>
        <name>Yee, Brian A</name>
      </author>
      <author>
        <name>Chen, Renee</name>
      </author>
      <author>
        <name>Yeo, Gene W</name>
      </author>
      <author>
        <name>Chen, Chun-Wei</name>
      </author>
      <author>
        <name>Chen, Liang</name>
      </author>
      <author>
        <name>Zheng, Sika</name>
        <uri>https://orcid.org/0000-0002-0573-4981</uri>
      </author>
    </item>
    <item>
      <title>Sex Differences in Opioid and Psychostimulant Craving and Relapse: A Critical Review</title>
      <link>https://escholarship.org/uc/item/836694fh</link>
      <description>A widely held dogma in the preclinical addiction field is that females are more vulnerable than males to drug craving and relapse. Here, we first review clinical studies on sex differences in psychostimulant and opioid craving and relapse. Next, we review preclinical studies on sex differences in psychostimulant and opioid reinstatement of drug seeking after extinction of drug self-administration, and incubation of drug craving (time-dependent increase in drug seeking during abstinence). We also discuss ovarian hormones' role in relapse and craving in humans and animal models and speculate on brain mechanisms underlying their role in cocaine craving and relapse in rodent models. Finally, we discuss imaging studies on brain responses to cocaine cues and stress in men and women.The results of the clinical studies reviewed do not appear to support the notion that women are more vulnerable to psychostimulant and opioid craving and relapse. However, this conclusion is tentative because...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/836694fh</guid>
      <pubDate>Sat, 11 May 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Nicolas, Céline</name>
      </author>
      <author>
        <name>Zlebnik, Natalie E</name>
      </author>
      <author>
        <name>Farokhnia, Mehdi</name>
      </author>
      <author>
        <name>Leggio, Lorenzo</name>
      </author>
      <author>
        <name>Ikemoto, Satoshi</name>
      </author>
      <author>
        <name>Shaham, Yavin</name>
      </author>
      <author>
        <name>Nader, Michael</name>
      </author>
    </item>
    <item>
      <title>Mechanisms underlying HIV-associated cognitive impairment and emerging therapies for its management</title>
      <link>https://escholarship.org/uc/item/0tt0x846</link>
      <description>People living with HIV are affected by the chronic consequences of neurocognitive impairment (NCI) despite antiretroviral therapies that suppress viral replication, improve health and extend life. Furthermore, viral suppression does not eliminate the virus, and remaining infected cells may continue to produce viral proteins that trigger neurodegeneration. Comorbidities such as diabetes mellitus are likely to contribute substantially to CNS injury in people living with HIV, and some components of antiretroviral therapy exert undesirable side effects on the nervous system. No treatment for HIV-associated NCI has been approved by the European Medicines Agency or the US Food and Drug Administration. Historically, roadblocks to developing effective treatments have included a limited understanding of the pathophysiology of HIV-associated NCI and heterogeneity in its clinical manifestations. This heterogeneity might reflect multiple underlying causes that differ among individuals, rather...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0tt0x846</guid>
      <pubDate>Sat, 11 May 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Ellis, Ronald J</name>
      </author>
      <author>
        <name>Marquine, María J</name>
      </author>
      <author>
        <name>Kaul, Marcus</name>
      </author>
      <author>
        <name>Fields, Jerel Adam</name>
      </author>
      <author>
        <name>Schlachetzki, Johannes CM</name>
        <uri>https://orcid.org/0000-0002-7801-9743</uri>
      </author>
    </item>
    <item>
      <title>Numb positively regulates Hedgehog signaling at the ciliary pocket</title>
      <link>https://escholarship.org/uc/item/6b09s5bd</link>
      <description>Hedgehog (Hh) signaling relies on the primary cilium, a cell surface organelle that serves as a signaling hub for the cell. Using proximity labeling and quantitative proteomics, we identify Numb as a ciliary protein that positively regulates Hh signaling. Numb localizes to the ciliary pocket and acts as an endocytic adaptor to incorporate Ptch1 into clathrin-coated vesicles, thereby promoting Ptch1 exit from the cilium, a key step in Hh signaling activation. Numb loss impedes Sonic hedgehog (Shh)-induced Ptch1 exit from the cilium, resulting in reduced Hh signaling. Numb loss in spinal neural progenitors reduces Shh-induced differentiation into cell fates reliant on high Hh activity. Genetic ablation of Numb in the developing cerebellum impairs the proliferation of granule cell precursors, a Hh-dependent process, resulting in reduced cerebellar size. This study highlights Numb as a regulator of ciliary Ptch1 levels during Hh signal activation and demonstrates the key role of ciliary...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6b09s5bd</guid>
      <pubDate>Fri, 3 May 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Liu, Xiaoliang</name>
        <uri>https://orcid.org/0009-0008-9296-9025</uri>
      </author>
      <author>
        <name>Yam, Patricia T</name>
      </author>
      <author>
        <name>Schlienger, Sabrina</name>
      </author>
      <author>
        <name>Cai, Eva</name>
      </author>
      <author>
        <name>Zhang, Jingyi</name>
      </author>
      <author>
        <name>Chen, Wei-Ju</name>
      </author>
      <author>
        <name>Torres Gutierrez, Oscar</name>
      </author>
      <author>
        <name>Jimenez Amilburu, Vanesa</name>
      </author>
      <author>
        <name>Ramamurthy, Vasanth</name>
      </author>
      <author>
        <name>Ting, Alice Y</name>
      </author>
      <author>
        <name>Branon, Tess C</name>
      </author>
      <author>
        <name>Cayouette, Michel</name>
      </author>
      <author>
        <name>Gen, Risako</name>
      </author>
      <author>
        <name>Marks, Tessa</name>
      </author>
      <author>
        <name>Kong, Jennifer H</name>
      </author>
      <author>
        <name>Charron, Frédéric</name>
      </author>
      <author>
        <name>Ge, Xuecai</name>
        <uri>https://orcid.org/0000-0002-5896-0800</uri>
      </author>
    </item>
    <item>
      <title>Toward decolonized fiscal relationships between universities and community organizations: lessons learned from the California community engagement alliance against COVID-19</title>
      <link>https://escholarship.org/uc/item/0g5421g9</link>
      <description>In September 2020 the US National Institutes of Health (NIH) allocated $12 million to support engagement with historically marginalized communities hardest hit by COVID-19. The award was designed to mobilize community-engagement in pandemic response, and to support partnerships as part of the NIH Community Engagement Alliance (CEAL) Against COVID-19 Disparities. All aspects of the award were fast-tracked and NIH utilized a 'more flexible' funding mechanism (OTA) to facilitate swift distribution of funds. In this paper, we draw upon an analysis of findings from a 2021 survey conducted with 11 California CEAL sites representing urban and rural settings, private and public universities, and established and new community partners and qualitative analysis of 2020-2022 site-wide meeting minutes. We describe challenges posed at the federal (e.g., NIH funding), university, and community-university partnership levels as well as opportunities and creative workarounds. Challenges include...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0g5421g9</guid>
      <pubDate>Fri, 26 Apr 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Burke, Nancy J</name>
        <uri>https://orcid.org/0000-0002-2269-3341</uri>
      </author>
      <author>
        <name>Espinosa, Patricia Rodriguez</name>
      </author>
      <author>
        <name>Corchado, Claudia C</name>
      </author>
      <author>
        <name>Vázquez, Evelyn</name>
      </author>
      <author>
        <name>Rosas, Lisa G</name>
      </author>
      <author>
        <name>Wooe, Kent J</name>
      </author>
      <author>
        <name>LeSarre, Monique</name>
      </author>
      <author>
        <name>Gallegos-Castillo, Angela</name>
      </author>
      <author>
        <name>Cheney, Ann</name>
        <uri>https://orcid.org/0000-0002-4032-6692</uri>
      </author>
      <author>
        <name>Lo, David D</name>
        <uri>https://orcid.org/0000-0002-5962-9458</uri>
      </author>
      <author>
        <name>Hintz, Rachel</name>
      </author>
      <author>
        <name>Vassar, Stefanie D</name>
      </author>
      <author>
        <name>Brown, Arleen F</name>
        <uri>https://orcid.org/0000-0001-9948-8955</uri>
      </author>
    </item>
    <item>
      <title>Cholinergic Neurotransmission Controls Orexigenic Endocannabinoid Signaling in the Gut in Diet-Induced Obesity.</title>
      <link>https://escholarship.org/uc/item/06m8h7sm</link>
      <description>The brain bidirectionally communicates with the gut to control food intake and energy balance, which becomes dysregulated in obesity. For example, endocannabinoid (eCB) signaling in the small-intestinal (SI) epithelium is upregulated in diet-induced obese (DIO) mice and promotes overeating by a mechanism that includes inhibiting gut-brain satiation signaling. Upstream neural and molecular mechanism(s) involved in overproduction of orexigenic gut eCBs in DIO, however, are unknown. We tested the hypothesis that overactive parasympathetic signaling at the muscarinic acetylcholine receptors (mAChRs) in the SI increases biosynthesis of the eCB, 2-arachidonoyl-&lt;i&gt;sn&lt;/i&gt;-glycerol (2-AG), which drives hyperphagia via local CB&lt;sub&gt;1&lt;/sub&gt;Rs in DIO. Male mice were maintained on a high-fat/high-sucrose Western-style diet for 60 d, then administered several mAChR antagonists 30 min prior to tissue harvest or a food intake test. Levels of 2-AG and the activity of its metabolic enzymes in the...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/06m8h7sm</guid>
      <pubDate>Thu, 25 Apr 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Wood, Courtney P</name>
      </author>
      <author>
        <name>Alvarez, Camila</name>
      </author>
      <author>
        <name>DiPatrizio, Nicholas V</name>
        <uri>https://orcid.org/0000-0001-8423-0695</uri>
      </author>
    </item>
    <item>
      <title>Advances in AI for Protein Structure Prediction: Implications for Cancer Drug Discovery and Development</title>
      <link>https://escholarship.org/uc/item/94p5s58p</link>
      <description>Recent advancements in AI-driven technologies, particularly in protein structure prediction, are significantly reshaping the landscape of drug discovery and development. This review focuses on the question of how these technological breakthroughs, exemplified by AlphaFold2, are revolutionizing our understanding of protein structure and function changes underlying cancer and improve our approaches to counter them. By enhancing the precision and speed at which drug targets are identified and drug candidates can be designed and optimized, these technologies are streamlining the entire drug development process. We explore the use of AlphaFold2 in cancer drug development, scrutinizing its efficacy, limitations, and potential challenges. We also compare AlphaFold2 with other algorithms like ESMFold, explaining the diverse methodologies employed in this field and the practical effects of these differences for the application of specific algorithms. Additionally, we discuss the broader...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/94p5s58p</guid>
      <pubDate>Mon, 15 Apr 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Qiu, Xinru</name>
      </author>
      <author>
        <name>Li, Han</name>
      </author>
      <author>
        <name>Steeg, Greg Ver</name>
      </author>
      <author>
        <name>Godzik, Adam</name>
      </author>
    </item>
    <item>
      <title>Acute pharmacological inhibition of matrix metalloproteinase‐9 activity during development restores perineuronal net formation and normalizes auditory processing in Fmr1 KO mice</title>
      <link>https://escholarship.org/uc/item/9nt9d53g</link>
      <description>Individuals with Fragile X Syndrome (FXS) and autism spectrum disorder (ASD) exhibit cognitive impairments, social deficits, increased anxiety, and sensory hyperexcitability. Previously, we showed that elevated levels of matrix metalloproteinase-9 (MMP-9) may contribute to abnormal development of parvalbumin (PV) interneurons and perineuronal nets (PNNs) in the developing auditory cortex (AC) of Fmr1 knock-out (KO) mice, which likely underlie auditory hypersensitivity. Thus, MMP-9 may serve as a potential target for treatment of auditory hypersensitivity in FXS. Here, we used the MMP-2/9 inhibitor, SB-3CT, to pharmacologically inhibit MMP-9 activity during a specific developmental period and to test whether inhibition of MMP-9 activity reverses neural oscillation deficits and behavioral impairments by enhancing PNN formation around PV cells in Fmr1 KO mice. Electroencephalography (EEG) was used to measure resting state and sound-evoked electrocortical activity in auditory and...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9nt9d53g</guid>
      <pubDate>Mon, 8 Apr 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Pirbhoy, Patricia S</name>
      </author>
      <author>
        <name>Rais, Maham</name>
      </author>
      <author>
        <name>Lovelace, Jonathan W</name>
      </author>
      <author>
        <name>Woodard, Walker</name>
      </author>
      <author>
        <name>Razak, Khaleel A</name>
      </author>
      <author>
        <name>Binder, Devin K</name>
      </author>
      <author>
        <name>Ethell, Iryna M</name>
        <uri>https://orcid.org/0000-0002-1324-6611</uri>
      </author>
    </item>
    <item>
      <title>A Twist between ROS and Sperm-Mediated Intergenerational Epigenetic Inheritance</title>
      <link>https://escholarship.org/uc/item/7qm7p5p5</link>
      <description>Yoshida et&amp;nbsp;al. (2020) report in this issue of Molecular Cell that a paternal low-protein diet elevates ROS in the testicular germ cells, altering ATF7 activity and H3K9me2 abundance on target genes, including tRNA loci. These changes are maintained in spermatozoa, regulating tsRNA biogenesis, and together transmit intergenerational effects.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7qm7p5p5</guid>
      <pubDate>Mon, 8 Apr 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Zhang, Xudong</name>
      </author>
      <author>
        <name>Chen, Qi</name>
        <uri>https://orcid.org/0000-0001-6353-9589</uri>
      </author>
    </item>
    <item>
      <title>Retraction: Site‐specific recombination of nitrogen‐fixation genes in cyanobacteria by XisF–XisH–XisI complex: Structures and models, William C. Hwang, James W. Golden, Jaime Pascual, Dong Xu, Anton Cheltsov, Adam Godzik</title>
      <link>https://escholarship.org/uc/item/49b686kz</link>
      <description>The above article from the Proteins: Structure, Function, and Bioinformatics, published online on 1 September 2014 in Wiley Online Library as Accepted Article (http://onlinelibrary.wiley.com/doi/10.1002/prot.24679/full), has been retracted by agreement between William C. Hwang, James W. Golden, Jaime Pascual, Dong Xu, Anton Cheltsov, Adam Godzik, the Editor‐in‐Chief, Bertrand E. Garcia‐Moreno, and Wiley Periodicals, Inc. The retraction has been agreed because submission was made without agreement from co‐author Adam Godzik.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/49b686kz</guid>
      <pubDate>Sun, 7 Apr 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Hwang, William C</name>
      </author>
      <author>
        <name>Golden, James W</name>
        <uri>https://orcid.org/0000-0001-5463-3207</uri>
      </author>
      <author>
        <name>Pascual, Jaime</name>
      </author>
      <author>
        <name>Xu, Dong</name>
      </author>
      <author>
        <name>Cheltsov, Anton</name>
      </author>
      <author>
        <name>Godzik, Adam</name>
      </author>
    </item>
    <item>
      <title>Developmental Attenuation of Neuronal Apoptosis by Neural-Specific Splicing of Bak1 Microexon</title>
      <link>https://escholarship.org/uc/item/2nf1g7z1</link>
      <description>Continuous neuronal survival is vital for mammals because mammalian brains have limited regeneration capability. After neurogenesis, suppression of apoptosis is needed to ensure a neuron's long-term survival. Here we describe a robust genetic program that intrinsically attenuates apoptosis competence in neurons. Developmental downregulation of the splicing regulator PTBP1 in immature neurons allows neural-specific splicing of the evolutionarily conserved Bak1 microexon 5. Exon 5 inclusion triggers nonsense-mediated mRNA decay (NMD) and unproductive translation of Bak1 transcripts (N-Bak mRNA), leading to suppression of pro-apoptotic BAK1 proteins and allowing neurons to reduce apoptosis. Germline heterozygous ablation of exon 5 increases BAK1 proteins exclusively in the brain, inflates neuronal apoptosis, and leads to early postnatal mortality. Therefore, neural-specific exon 5 splicing and depletion of BAK1 proteins uniquely repress neuronal apoptosis. Although apoptosis is important...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2nf1g7z1</guid>
      <pubDate>Fri, 22 Mar 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Lin, Lin</name>
      </author>
      <author>
        <name>Zhang, Min</name>
      </author>
      <author>
        <name>Stoilov, Peter</name>
      </author>
      <author>
        <name>Chen, Liang</name>
      </author>
      <author>
        <name>Zheng, Sika</name>
      </author>
    </item>
    <item>
      <title>A critical role for Macrophage-derived Cysteinyl-Leukotrienes in HIV-1 induced neuronal injury</title>
      <link>https://escholarship.org/uc/item/6887n486</link>
      <description>Macrophages (MΦ) infected with human immunodeficiency virus (HIV)-1 or activated by its envelope protein gp120 exert neurotoxicity. We found previously that signaling via p38 mitogen-activated protein kinase (p38 MAPK) is essential to the neurotoxicity of HIVgp120-stimulated MΦ. However, the associated downstream pathways remained elusive. Here we show that cysteinyl-leukotrienes (CysLT) released by HIV-infected or HIVgp120 stimulated MΦ downstream of p38 MAPK critically contribute to neurotoxicity. SiRNA-mediated or pharmacological inhibition of p38 MAPK deprives MΦ of CysLT synthase (LTC4S) and, pharmacological inhibition of the cysteinyl-leukotriene receptor 1 (CYSLTR1) protects cerebrocortical neurons against toxicity of both gp120-stimulated and HIV-infected MΦ. Components of the CysLT pathway are differentially regulated in brains of HIV-infected individuals and a transgenic mouse model of NeuroHIV (HIVgp120tg). Moreover, genetic ablation of LTC4S or CysLTR1 prevents neuronal...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6887n486</guid>
      <pubDate>Thu, 21 Mar 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Yuan, Nina Y</name>
      </author>
      <author>
        <name>Medders, Kathryn E</name>
      </author>
      <author>
        <name>Sanchez, Ana B</name>
      </author>
      <author>
        <name>Shah, Rohan</name>
      </author>
      <author>
        <name>de Rozieres, Cyrus M</name>
      </author>
      <author>
        <name>Ojeda-Juárez, Daniel</name>
      </author>
      <author>
        <name>Maung, Ricky</name>
      </author>
      <author>
        <name>Williams, Roy</name>
      </author>
      <author>
        <name>Gelman, Benjamin B</name>
      </author>
      <author>
        <name>Baaten, Bas J</name>
      </author>
      <author>
        <name>Roberts, Amanda J</name>
      </author>
      <author>
        <name>Kaul, Marcus</name>
      </author>
    </item>
    <item>
      <title>A standardized ontology for naming tRNA-derived RNAs based on molecular origin</title>
      <link>https://escholarship.org/uc/item/5rt6308c</link>
      <description>A standardized ontology for naming tRNA-derived RNAs based on molecular origin</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5rt6308c</guid>
      <pubDate>Mon, 11 Mar 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Holmes, Andrew D</name>
      </author>
      <author>
        <name>Chan, Patricia P</name>
        <uri>https://orcid.org/0000-0003-0810-1642</uri>
      </author>
      <author>
        <name>Chen, Qi</name>
        <uri>https://orcid.org/0000-0001-6353-9589</uri>
      </author>
      <author>
        <name>Ivanov, Pavel</name>
      </author>
      <author>
        <name>Drouard, Laurence</name>
      </author>
      <author>
        <name>Polacek, Norbert</name>
      </author>
      <author>
        <name>Kay, Mark A</name>
      </author>
      <author>
        <name>Lowe, Todd M</name>
      </author>
    </item>
    <item>
      <title>Harnessing preexisting influenza virus-specific immunity increases antibody responses against SARS-CoV-2</title>
      <link>https://escholarship.org/uc/item/1056c8gq</link>
      <description>In pandemic scenarios involving novel human pathogenic viruses, it is highly desirable that vaccines induce strong neutralizing antibodies as quickly as possible. However, current vaccine strategies require multiple immunization doses to produce high titers of neutralizing antibodies and are poorly protective after a single vaccination. We therefore wished to design a vaccine candidate that would induce increased protective immune responses following the first vaccine dose. We hypothesized that antibodies against the receptor-binding domain (RBD) of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike glycoprotein could be increased by drawing upon immunity to a previous infection. We generated a fusion protein containing the influenza H1N1 PR8 virus nucleoprotein (NP) and the SARS-CoV-2 spike RBD. Mice with or without preexisting immunity to PR8 were then vaccinated with NP/RBD. We observed significantly increased SARS-CoV-2 neutralizing antibodies in mice with...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1056c8gq</guid>
      <pubDate>Fri, 1 Mar 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Dulin, Harrison</name>
      </author>
      <author>
        <name>Barre, Ramya S</name>
      </author>
      <author>
        <name>Xu, Duo</name>
      </author>
      <author>
        <name>Neal, Arrmund</name>
      </author>
      <author>
        <name>Vizcarra, Edward</name>
      </author>
      <author>
        <name>Chavez, Jerald</name>
      </author>
      <author>
        <name>Ulu, Arzu</name>
      </author>
      <author>
        <name>Yang, Myeon-Sik</name>
      </author>
      <author>
        <name>Khan, Siddiqur Rahman</name>
      </author>
      <author>
        <name>Wuang, Keidy</name>
      </author>
      <author>
        <name>Bhakta, Nikhil</name>
      </author>
      <author>
        <name>Chea, Chanvoraboth</name>
      </author>
      <author>
        <name>Wilson, Emma H</name>
        <uri>https://orcid.org/0000-0002-6054-9981</uri>
      </author>
      <author>
        <name>Martinez-Sobrido, Luis</name>
      </author>
      <author>
        <name>Hai, Rong</name>
        <uri>https://orcid.org/0000-0003-4173-4521</uri>
      </author>
    </item>
    <item>
      <title>Impacts of Caffeine during Pregnancy</title>
      <link>https://escholarship.org/uc/item/4p52t7h5</link>
      <description>Epidemiological studies have revealed that caffeine consumption during pregnancy is associated with adverse gestational outcomes, yet the underlying mechanisms remain obscure. Recent animal studies with physiologically relevant dosages have begun to dissect adverse effects of caffeine during pregnancy with respect to oviduct contractility, embryo development, uterine receptivity, and placentation that jointly contribute to pregnancy complications. Interestingly, caffeine's effects are highly variable between individual animals under well-controlled experimental settings, suggesting the possibility of epigenetic regulation of these phenotypes, in addition to genetic variants. Moreover, caffeine exposure during sensitive windows of pregnancy may induce epigenetic changes in the developing fetus or even the germ cells to cause adult-onset diseases in subsequent generations. We discuss these research frontiers in light of emerging data.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4p52t7h5</guid>
      <pubDate>Sun, 25 Feb 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Qian, Jingjing</name>
      </author>
      <author>
        <name>Chen, Qi</name>
        <uri>https://orcid.org/0000-0001-6353-9589</uri>
      </author>
      <author>
        <name>Ward, Sean M</name>
      </author>
      <author>
        <name>Duan, Enkui</name>
      </author>
      <author>
        <name>Zhang, Ying</name>
      </author>
    </item>
    <item>
      <title>Acute Simian Varicella Virus Infection Causes Robust and Sustained Changes in Gene Expression in the Sensory Ganglia</title>
      <link>https://escholarship.org/uc/item/1km9s981</link>
      <description>Primary infection with varicella-zoster virus (VZV), a neurotropic alphaherpesvirus, results in varicella. VZV establishes latency in the sensory ganglia and can reactivate later in life to cause herpes zoster. The relationship between VZV and its host during acute infection in the sensory ganglia is not well understood due to limited access to clinical specimens. Intrabronchial inoculation of rhesus macaques with simian varicella virus (SVV) recapitulates the hallmarks of VZV infection in humans. We leveraged this animal model to characterize the host-pathogen interactions in the ganglia during both acute and latent infection by measuring both viral and host transcriptomes on days postinfection (dpi) 3, 7, 10, 14, and 100. SVV DNA and transcripts were detected in sensory ganglia 3 dpi, before the appearance of rash. CD4 and CD8 T cells were also detected in the sensory ganglia 3 dpi. Moreover, lung-resident T cells isolated from the same animals 3 dpi also harbored SVV DNA and...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1km9s981</guid>
      <pubDate>Fri, 16 Feb 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Arnold, Nicole</name>
      </author>
      <author>
        <name>Girke, Thomas</name>
        <uri>https://orcid.org/0000-0003-0710-3777</uri>
      </author>
      <author>
        <name>Sureshchandra, Suhas</name>
      </author>
      <author>
        <name>Messaoudi, Ilhem</name>
      </author>
    </item>
    <item>
      <title>Alcohol Consumption Modulates Host Defense in Rhesus Macaques by Altering Gene Expression in Circulating Leukocytes</title>
      <link>https://escholarship.org/uc/item/0gj5h3pb</link>
      <description>Several lines of evidence indicate that chronic alcohol use disorder leads to increased susceptibility to several viral and bacterial infections, whereas moderate alcohol consumption decreases the incidence of colds and improves immune responses to some pathogens. In line with these observations, we recently showed that heavy ethanol intake (average blood ethanol concentrations &amp;gt; 80 mg/dl) suppressed, whereas moderate alcohol consumption (blood ethanol concentrations &amp;lt; 50 mg/dl) enhanced, T and B cell responses to modified vaccinia Ankara vaccination in a nonhuman primate model of voluntary ethanol consumption. To uncover the molecular basis for impaired immunity with heavy alcohol consumption and enhanced immune response with moderate alcohol consumption, we performed a transcriptome analysis using PBMCs isolated on day 7 post-modified vaccinia Ankara vaccination, the earliest time point at which we detected differences in T cell and Ab responses. Overall, chronic heavy...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0gj5h3pb</guid>
      <pubDate>Fri, 16 Feb 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Barr, Tasha</name>
      </author>
      <author>
        <name>Girke, Thomas</name>
        <uri>https://orcid.org/0000-0003-0710-3777</uri>
      </author>
      <author>
        <name>Sureshchandra, Suhas</name>
      </author>
      <author>
        <name>Nguyen, Christina</name>
      </author>
      <author>
        <name>Grant, Kathleen</name>
      </author>
      <author>
        <name>Messaoudi, Ilhem</name>
      </author>
    </item>
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