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Sensing bacterial infections by NAIP receptors in NLRC4 inflammasome activation

机译:NAIP受体在NLRC4炎性小体激活中感知细菌感染

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The inflammasome is an emerging new pathway in innate immune defense against microbial infection or endogenous danger signals. The inflammasome stimulates activation of inflammatory caspases, mainly caspase-1. Caspase-1 activation is responsible for processing and secretion of IL-1β and IL-18 as well as for inducing macrophage pyroptotic death. Assembly of the large cytoplasmic inflammasome complex is thought to be mediated by members of NOD-like receptor (NLR) family. While functions of most of the NLR proteins remain to be defined, several NLR proteins including NLRC4 have been shown to assemble distinct inflammasome complexes. These inflammasome pathways, particularly the NLRC4 inflammasome, play a critical role in sensing and restricting diverse types of bacterial infections. Here we review recent advances in defining the exact bacterial ligands and the ligand-binding receptors involved in NLRC4 inflammasome activation. Implications of the discovery of the NAIP family of inflammasome receptors for bacterial flagellin and type III secretion apparatus on future inflammasome and bacterial infection studies are also discussed.
机译:炎症小体是针对微生物感染或内源性危险信号的先天免疫防御的新兴途径。炎性小体刺激炎性胱天蛋白酶,主要是胱天蛋白酶-1的活化。 Caspase-1激活负责IL-1β和IL-18的加工和分泌,并诱导巨噬细胞烧死。大细胞质炎性体复合物的组装被认为是由NOD样受体(NLR)家族成员介导的。尽管大多数NLR蛋白的功能尚待确定,但已显示包括NLRC4在内的几种NLR蛋白可组装不同的炎症小体复合物。这些炎性体途径,尤其是NLRC4炎性体,在感知和限制各种细菌感染中起着关键作用。在这里,我们回顾了在定义确切的细菌配体和参与NLRC4炎症小体激活的配体结合受体方面的最新进展。还讨论了细菌鞭毛蛋白和III型分泌装置的NAIP炎性体受体家族的发现对未来炎性体和细菌感染研究的意义。

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