Influenza virus activates inflammasomes via its intracellular M2 ion channel

被引:583
作者
Ichinohe, Takeshi [1 ]
Pang, Iris K. [1 ]
Iwasaki, Akiko [1 ]
机构
[1] Yale Univ, Sch Med, Dept Immunobiol, New Haven, CT 06520 USA
基金
日本学术振兴会; 美国国家卫生研究院;
关键词
A VIRUS; STRANDED-RNA; NALP3; INFLAMMASOME; IMMUNE-RESPONSES; CYTOPLASMIC DNA; RIG-I; INNATE; CASPASE-1; INFECTION; PROTEIN;
D O I
10.1038/ni.1861
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Influenza virus, a negative-stranded RNA virus that causes severe illness in humans and animals, stimulates the inflammasome through the Nod-like receptor NLRP3. However, the mechanism by which influenza virus activates the NLRP3 inflammasome is unknown. Here we show that the influenza virus M2 protein, a proton-selective ion channel important in viral pathogenesis, stimulates the NLRP3 inflammasome pathway. M2 channel activity was required for the activation of inflammasomes by influenza and was sufficient to activate inflammasomes in primed macrophages and dendritic cells. M2-induced activation of inflammasomes required its localization to the Golgi apparatus and was dependent on the pH gradient. Our results show a mechanism by which influenza virus infection activates inflammasomes and identify the sensing of disturbances in intracellular ionic concentrations as a previously unknown pathogen-recognition pathway.
引用
收藏
页码:404 / U61
页数:8
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