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Role of CFTR expressed by neutrophils in modulating acute lung inflammation and injury in mice.
- Author(s): Su, Xiao;
- Looney, Mark R;
- Su, Hang Emily;
- Lee, Jae Woo;
- Song, Yuanlin;
- Matthay, Michael A
- et al.
Published Web Locationhttps://doi.org/10.1007/s00011-011-0313-x
Objective and designCystic fibrosis transmembrane conductance regulator (CFTR) regulates infection and inflammation. In this study, we investigated whether a lack of functional CFTR in neutrophils would promote lipopolysaccharide (LPS)-induced lung inflammation and injury.
Materials and methodsCFTR-inhibited or F508del-CFTR-mutated neutrophils were stimulated with LPS and cultured to evaluate production of cytokines and NF-κB activation. Wild-type mice were reconstituted with F508del neutrophils or bone marrow and then intratracheally challenged with LPS to observe lung inflammatory response.
ResultsPharmacologic inhibition and genetic mutation of CFTR in neutrophils activated NF-κB and facilitated macrophage inflammatory protein-2 (MIP-2) and tumor necrosis factor-α (TNF-α) production. Wild-type mice reconstituted with F508del neutrophils and bone marrow had more severe lung inflammation and injury after LPS challenge compared to wild-type mice receiving wild-type neutrophils or bone marrow reconstitution.
ConclusionsLack of functional CFTR in neutrophils can promote LPS-induced acute lung inflammation and injury.
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