Inflammasomes: caspase-1-activating platforms with critical roles in host defense

被引:33
|
作者
Vande Walle, Lieselotte [1 ,2 ]
Lamkanfi, Mohamed [1 ,2 ]
机构
[1] Univ Ghent, Dept Biochem, Albert Baertsoenkaai 3, B-9000 Ghent, Belgium
[2] Vlaams Inst Biotechnol, Dept Med Prot Res, Ghent, Belgium
来源
关键词
caspase-1; inflammasome; NOD-like receptors; pathogen; interleukin; pyroptosis; infection; GAMMA-INDUCING FACTOR; VIRUS SERPIN; INTERLEUKIN-1-BETA-CONVERTING ENZYME; CASPASE-1; ACTIVATION; IMMUNE RECOGNITION; AIM2; INFLAMMASOME; CONVERTING-ENZYME; DOMAIN PROTEIN; MICE DEFICIENT; B13R SPI-2;
D O I
10.3389/fmicb.2011.00003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Activation of the inflammatory cysteine protease caspase-1 in inflammasome complexes plays a critical role in the host response to microbial infections. Inflammasome activation induces inflammation through secretion of the pro-inflammatory cytokines interleukin (IL)-1 beta and IL-18 and through extracellular release of the alarmin high mobility group box 1. Moreover, caspase-1 activation by inflammasomes counters bacterial replication and induces pyroptosis, a specialized cell death program that removes infected immune cells as part of the host defense system. It is thus not surprising that bacterial and viral pathogens evolved virulence factors targeting inflammasome activation and activity. Here, we provide an overview of the distinct inflammasome complexes that are activated in a pathogen-specific manner and discuss the diverse strategies employed by viruses and bacteria to modulate inflammasome function.
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页数:6
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