| Literature DB >> 31435009 |
Angel G Solis1, Piotr Bielecki1, Holly R Steach1, Lokesh Sharma2, Christian C D Harman3, Sanguk Yun4,5,6, Marcel R de Zoete7, James N Warnock8, S D Filip To9, Autumn G York1, Matthias Mack10, Martin A Schwartz4,5,6, Charles S Dela Cruz2, Noah W Palm1, Ruaidhrí Jackson11, Richard A Flavell12,13.
Abstract
Direct recognition of invading pathogens by innate immune cells is a critical driver of the inflammatory response. However, cells of the innate immune system can also sense their local microenvironment and respond to physiological fluctuations in temperature, pH, oxygen and nutrient availability, which are altered during inflammation. Although cells of the immune system experience force and pressure throughout their life cycle, little is known about how these mechanical processes regulate the immune response. Here we show that cyclical hydrostatic pressure, similar to that experienced by immune cells in the lung, initiates an inflammatory response via the mechanically activated ion channel PIEZO1. Mice lacking PIEZO1 in innate immune cells showed ablated pulmonary inflammation in the context of bacterial infection or fibrotic autoinflammation. Our results reveal an environmental sensory axis that stimulates innate immune cells to mount an inflammatory response, and demonstrate a physiological role for PIEZO1 and mechanosensation in immunity.Entities:
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Year: 2019 PMID: 31435009 PMCID: PMC6939392 DOI: 10.1038/s41586-019-1485-8
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962