Interaction between the inflammasome and commensal microorganisms in gastrointestinal health and disease

被引:36
作者
Watanabe, Daisuke [1 ]
Guo, Yijie [1 ]
Kamada, Nobuhiko [1 ]
机构
[1] Univ Michigan, Dept Internal Med, Div Gastroenterol & Hepatol, Ann Arbor, MI 48109 USA
基金
日本学术振兴会; 美国国家卫生研究院; 中国国家自然科学基金;
关键词
gut microbiota; inflammasome; interleukin; 18; 1; beta; AIM2; INFLAMMASOME; INTESTINAL HOMEOSTASIS; MACROPHAGE ACTIVATION; CASPASE-1; ACTIVATION; IMMUNE RECOGNITION; ULCERATIVE-COLITIS; NLRP3; INNATE IMMUNITY; HOST-DEFENSE; MICROBIOTA;
D O I
10.15252/emmm.202013452
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The inflammasome is a cytosolic multiprotein complex that plays a crucial role in inflammation and cell death. The sensor proteins in the inflammasome complex detect various microbial and endogenous stimuli, leading to subsequent caspase activation. The activation of caspases results in the maturation of pro-inflammatory cytokines IL-1 beta and IL-18 or pyroptosis. Inflammasome dysfunction is associated with the pathogenesis of various diseases, including autoimmune disease and cancer. It appears that the interactions between the gut microbiota and the inflammasome play crucial roles in the gastrointestinal tract. The gut microbiota induces the expression and activation of inflammasome proteins, which contribute to both homeostasis and disease in the gut. Likewise, although controversial, mounting evidence suggests that inflammasome activation can modulate the composition of the gut microbiota, which, in turn, affects disease progression. In this review, we summarize the current concepts and recent insights linking the inflammasome and gut commensal microorganisms. We describe how the reciprocal interaction between the inflammasome and the commensal microbiota relates to physiological and pathophysiological consequences in the host.
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页数:11
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