Bacterial exotoxins and the inflammasome

被引:83
|
作者
Greaney, Allison J. [1 ]
Leppla, Stephen H. [1 ]
Moayeri, Mahtab [1 ]
机构
[1] NIAID, Microbial Pathogenesis Sect, Parasit Dis Lab, NIH, Bethesda, MD 20892 USA
来源
FRONTIERS IN IMMUNOLOGY | 2015年 / 6卷
基金
美国国家卫生研究院;
关键词
inflammasome; caspase-1; interleukin-1; pyroptosis; exotoxins; NLRP3; Nod-like receptors; anthrax lethal toxin; ANTHRAX LETHAL TOXIN; PHENOL-SOLUBLE MODULINS; TUMOR-NECROSIS-FACTOR; NLRP3; INFLAMMASOME; CASPASE-1; AUTOPROTEOLYSIS; TH17; RESPONSES; CELL-DEATH; RHO GTPASES; K+ EFFLUX; ACTIVATION;
D O I
10.3389/fimmu.2015.00570
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The inflammasomes are intracellular protein complexes that play an important role in innate immune sensing. Activation of inflammasomes leads to activation of caspase-1 and maturation and secretion of the pro-inflammatory cytokines interleukin (IL)-1 alpha and IL-18. In certain myeloid cells, this activation can also lead to an inflammatory cell death (pyroptosis). Inflammasome sensor proteins have evolved to detect a range of microbial ligands and bacterial exotoxins either through direct interaction or by detection of host cell changes elicited by these effectors. Bacterial exotoxins activate the inflammasomes through diverse processes, including direct sensor cleavage, modulation of ion fluxes through plasma membrane pore formation, and perturbation of various host cell functions. In this review, we summarize the findings on some of the bacterial exotoxins that activate the inflammasomes.
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页数:10
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