Department of Biochemistry, Ghent University, Ghent 9000, Belgium.
Annu Rev Cell Dev Biol. 2012;28:137-61. doi: 10.1146/annurev-cellbio-101011-155745. Epub 2012 Sep 10.
Inflammasomes are a set of intracellular protein complexes that enable autocatalytic activation of inflammatory caspases, which drive host and immune responses by releasing cytokines and alarmins into circulation and by inducing pyroptosis, a proinflammatory cell death mode. The inflammasome type mediating these responses varies with the microbial pathogen or stress factor that poses a threat to the organism. Since the discovery that polymorphisms in inflammasome genes are linked to common autoimmune diseases and less frequent periodic fever syndromes, inflammasome signaling has been dissected at the molecular level. In this review, we present recently gained insight on the distinct inflammasome types, their activation and effector mechanisms, and their modulation by microbial virulence factors. In addition, we discuss recently gained knowledge on the role of deregulated inflammasome activity in human autoinflammatory, autoimmune, and infectious diseases.
炎症小体是一组细胞内蛋白复合物,能够使炎症性胱天蛋白酶发生自身催化激活,通过将细胞因子和警报素释放到循环中,并通过诱导细胞焦亡(一种促炎细胞死亡模式),从而驱动宿主和免疫反应。介导这些反应的炎症小体类型因威胁生物体的微生物病原体或应激因子而异。自从发现炎症小体基因的多态性与常见的自身免疫性疾病和较少见的周期性发热综合征有关以来,炎症小体信号已在分子水平上进行了剖析。在这篇综述中,我们介绍了最近在不同炎症小体类型、它们的激活和效应机制以及它们被微生物毒力因子调节方面的新见解。此外,我们还讨论了炎症小体活性失调在人类自身炎症性、自身免疫性和感染性疾病中的作用的最新认识。