National Institute of Biological Sciences, Beijing, 102206, China.
Protein Cell. 2012 Feb;3(2):98-105. doi: 10.1007/s13238-012-2028-3. Epub 2012 Mar 17.
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.
炎症小体是先天免疫防御微生物感染或内源性危险信号的新兴新途径。炎症小体刺激炎症半胱天冬酶的激活,主要是半胱天冬酶-1。半胱天冬酶-1 的激活负责加工和分泌白细胞介素-1β和白细胞介素-18 ,并诱导巨噬细胞焦亡死亡。大细胞质炎症小体复合物的组装被认为是由 NOD 样受体 (NLR) 家族成员介导的。虽然大多数 NLR 蛋白的功能仍有待确定,但已经证明包括 NLRC4 在内的几种 NLR 蛋白组装了不同的炎症小体复合物。这些炎症小体途径,特别是 NLRC4 炎症小体,在感知和限制多种类型的细菌感染方面起着至关重要的作用。本文综述了最近在确定 NLRC4 炎症小体激活中涉及的特定细菌配体和配体结合受体方面的进展。还讨论了 NAIP 家族炎症小体受体对细菌鞭毛和 III 型分泌装置的发现对未来炎症小体和细菌感染研究的意义。