炎症体
吡喃结构域
细胞生物学
细胞内
点头
化学
上睑下垂
NALP3
程序性细胞死亡
生物
半胱氨酸蛋白酶1
受体
生物化学
细胞凋亡
基因
作者
Karen V. Swanson,Meng Deng,Jenny P.‐Y. Ting
出处
期刊:Nature Reviews Immunology
[Springer Nature]
日期:2019-04-29
卷期号:19 (8): 477-489
被引量:3135
标识
DOI:10.1038/s41577-019-0165-0
摘要
NLRP3 (NOD-, LRR- and pyrin domain-containing protein 3) is an intracellular sensor that detects a broad range of microbial motifs, endogenous danger signals and environmental irritants, resulting in the formation and activation of the NLRP3 inflammasome. Assembly of the NLRP3 inflammasome leads to caspase 1-dependent release of the pro-inflammatory cytokines IL-1β and IL-18, as well as to gasdermin D-mediated pyroptotic cell death. Recent studies have revealed new regulators of the NLRP3 inflammasome, including new interacting or regulatory proteins, metabolic pathways and a regulatory mitochondrial hub. In this Review, we present the molecular, cell biological and biochemical bases of NLRP3 activation and regulation and describe how this mechanistic understanding is leading to potential therapeutics that target the NLRP3 inflammasome.
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