生物
NLRC4型
二十烷酸
细胞生物学
半胱氨酸蛋白酶1
炎症体
微生物学
免疫学
炎症
癌症研究
生物化学
酶
花生四烯酸
作者
Isabella Rauch,Katherine A. Deets,Daisy X. Ji,Jakob von Moltke,Jeannette L. Tenthorey,Angus Y. Lee,Naomi H. Philip,Janelle S. Ayres,Igor E. Brodsky,Karsten Gronert,Russell E. Vance
出处
期刊:Immunity
[Cell Press]
日期:2017-04-01
卷期号:46 (4): 649-659
被引量:402
标识
DOI:10.1016/j.immuni.2017.03.016
摘要
Intestinal epithelial cells (IECs) form a critical barrier against pathogen invasion. By generation of mice in which inflammasome expression is restricted to IECs, we describe a coordinated epithelium-intrinsic inflammasome response in vivo. This response was sufficient to protect against Salmonella tissue invasion and involved a previously reported IEC expulsion that was coordinated with lipid mediator and cytokine production and lytic IEC death. Excessive inflammasome activation in IECs was sufficient to result in diarrhea and pathology. Experiments with IEC organoids demonstrated that IEC expulsion did not require other cell types. IEC expulsion was accompanied by a major actin rearrangement in neighboring cells that maintained epithelium integrity but did not absolutely require Caspase-1 or Gasdermin D. Analysis of Casp1-/-Casp8-/- mice revealed a functional Caspase-8 inflammasome in vivo. Thus, a coordinated IEC-intrinsic, Caspase-1 and -8 inflammasome response plays a key role in intestinal immune defense and pathology.
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