The valley degree of freedom of electrons in two-dimensional transition metal dichalcogenides has been extensively studied by theory (1-4), optical (5-9), and optoelectronic (10-13) experiments. However, generation and detection of pure valley current without relying on optical selection have not yet been demonstrated in these materials. Here, we report that valley current can be electrically induced and detected through the valley Hall effect and inverse valley Hall effect, respectively, in monolayer molybdenum disulfide. We compare temperature and channel length dependence of nonlocal electrical signals in monolayer and multilayer samples to distinguish the valley Hall effect from classical ohmic contributions. Notably, valley transport is observed over a distance of 4 μm in monolayer samples at room temperature. Our findings will enable a new generation of electronic devices using the valley degree of freedom, which can be used for future novel valleytronic applications.

Low-barrier nanomagnets have attracted a great deal of research interest for their use as sources of high-quality true random number generation. More recently, low-barrier nanomagnets with tunable output have been shown to be a natural hardware platform for unconventional computing paradigms such as probabilistic spin logic. Efficient generation and tunability of high-quality random bits is critical for these novel applications. However, current spintronic random number generators are based on superparamagnetic tunnel junctions with tunability obtained through spin transfer torque, which unavoidably leads to challenges in designing concatenated networks using these two terminal devices. The more recent development of utilizing spin orbit torque (SOT) allows for a three-terminal device design, but can only tune in-plane magnetization freely, which is not very energy efficient due to the needs of overcoming a large demagnetization field. In this work, we experimentally demonstrate a stochastic device with perpendicular magnetic anisotropy that is completely tunable by SOT without the aid of any external magnetic field. Our measurements lead us to hypothesize that a tilted anisotropy might be responsible for the observed tunability. We carry out stochastic Landau-Lifshitz-Gilbert simulations to confirm our experimental observation. Finally, we build an electrically coupled network of two such stochastic nanomagnet-based devices and demonstrate that finite correlation or anticorrelation can be established between their output fluctuations by a weak interconnection, despite having a large difference in their natural fluctuation timescale. Simulations based on a dynamical model for autonomous circuits composed of low-barrier nanomagnets show close agreement with the experimental results.

Chronic obstructive pulmonary disease (COPD) is a highly heterogeneous disease, and metabolomics plays a hub role in predictive, preventive, and personalized medicine (PPPM) related to COPD. This study thus aimed to reveal the role of induced sputum metabolomics in predicting COPD severity. In this pilot study, a total of 20 COPD patients were included. The induced sputum metabolites were assayed using a liquid chromatography-mass spectrometry (LC-MS/MS) system. Five oxidative stress products (myeloperoxidase (MPO), superoxide dismutase (SOD), glutathione (GSH), neutrophil elastase (NE), and 8-iso-PGF2α) in induced sputum were measured by ELISA, and the metabolomic profiles were distinguished by principal component analysis (PCA) and orthogonal projections to latent structures discriminant analysis (OPLS-DA). The Kyoto Encyclopedia of Genes and Genomes (KEGG) was used for pathway enrichment analysis, and a significant difference in induced sputum metabolomics was observed between moderate and severe COPD. The KEGG analysis revealed that the glycerophospholipid metabolism pathway was downregulated in severe COPD. Due to the critical role of glycerophospholipid metabolism in oxidative stress, significant negative correlations were discovered between glycerophospholipid metabolites and three oxidative stress products (SOD, MPO, and 8-iso-PGF2α). The diagnostic values of SOD, MPO, and 8-iso-PGF2α in induced sputum were found to exhibit high sensitivities and specificities in the prediction of COPD severity. Collectively, this study provides the first identification of the association between induced sputum metabolomic profiles and COPD severity, indicating the potential value of metabolomics in PPPM for COPD management. The study also reveals the correlation between glycerophospholipid metabolites and oxidative stress products and their value for predicting COPD severity.

Supplementary information

The online version contains supplementary material available at 10.1007/s13167-020-00227-w.

Airway dendritic cells (DCs) are recognized as important factors in the mechanisms of allergic inflammatory diseases. Suppressor of cytokine signaling 3 (SOCS3) is involved in regulating the functions of T cells and macrophages, but the roles of SOCS3-expressing DCs in the pathogeneses of allergic inflammatory diseases are still controversial. We compared the effects of adoptively transferred SOCS3^-/- and SOCS3^+/+ bone marrow-derived DCs (BMDCs) on airway inflammation in ovalbumin (OVA)-sensitized asthmatic mice. Adoptive transfer of mature DCs (lipopolysaccharide [LPS]-induced DCs, DClps) with or without SOCS3 gene expression significantly ameliorated allergic airway inflammation. SOCS3^-/- DCs slightly attenuated BMDC-induced immunogenic tolerance. DClps migrated to OVA-sensitized lungs with higher efficiency than immature DCs (DCim). DClps with or without SOCS3 greatly improved lung pathology scores and alleviated airway inflammatory cell infiltration after adoptive transfer into mice; they also increased interleukin-10 (IL-10) and transforming growth factor-β (TGF-β) production and inhibited signal transducer and activator of transcription (STAT) 4 and STAT6 signaling in the lungs after OVA sensitization. In conclusion, the BMDC adoptive transfer-induced immunogenic tolerance in OVA-sensitized mice might not be due to SOCS3 gene depletion. BMDC adoptive transfer may be developed into a new approach that alleviates asthma by modulating the balance between immune tolerance and inflammation.