先天免疫系统
机械反应
免疫系统
炎症
机械敏感通道
免疫学
免疫
生物
背景(考古学)
压电1
经典补体途径
细胞生物学
补体系统
受体
离子通道
生物化学
古生物学
作者
Ángel G. Alpuche‐Solís,Piotr Bielecki,Holly R. Steach,Lokesh Sharma,Christian C. D. Harman,Sanguk Yun,Marcel R. de Zoete,J. Warnock,S. D. Filip To,Autumn G. York,Matthias Mack,Martin A. Schwartz,Charles S. Dela Cruz,Noah W. Palm,Ruaidhrí Jackson,Richard A. Flavell
出处
期刊:Nature
[Springer Nature]
日期:2019-08-21
卷期号:573 (7772): 69-74
被引量:438
标识
DOI:10.1038/s41586-019-1485-8
摘要
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.
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