Department of Microbiology and Immunology and Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Department of Microbiology and Immunology and Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Curr Opin Microbiol. 2014 Feb;17:61-6. doi: 10.1016/j.mib.2013.11.008. Epub 2013 Dec 22.
The sanctity of the cytosolic compartment is rigorously maintained by a number of innate immune mechanisms. Inflammasomes detect signatures of microbial infection and trigger caspase-1 or caspase-11 activation, culminating in cytokine secretion and obliteration of the replicative niche via pyroptosis. Recent studies have examined inflammatory caspase responses to cytosolic bacteria, including Burkholderia, Shigella, Listeria, Francisella, and Mycobacterium species. For example, caspase-11 responds to LPS introduced into the cytosol after Gram-negative bacteria escape the vacuole. Not surprisingly, bacteria antagonize these responses; for example, Shigella delivers OspC3 to inhibit caspase-4, a potential human homolog of murine caspase-11. These findings underscore bacterial coevolution with the innate immune system, which has resulted in few, but highly specialized cytosolic pathogens.
细胞质区室的神圣性受到多种先天免疫机制的严格维护。炎症小体检测微生物感染的特征,并触发 caspase-1 或 caspase-11 的激活,最终导致细胞因子的分泌和通过细胞焦亡来破坏复制龛位。最近的研究检查了炎症性 caspase 对细胞质细菌的反应,包括伯克霍尔德菌、志贺氏菌、李斯特菌、弗朗西斯菌和分枝杆菌属。例如,caspase-11 对革兰氏阴性细菌从吞噬体逃逸后进入细胞质的 LPS 作出反应。毫不奇怪,细菌会拮抗这些反应;例如,志贺氏菌递送 OspC3 以抑制潜在的人类 caspase-11 的鼠源同源物 caspase-4。这些发现强调了细菌与先天免疫系统的共同进化,这导致了少数但高度特化的细胞质病原体。