Department of Immunology and Microbiology, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Laboratory of Molecular Biology and Physiology of Streptococci, Institute of Biology Roberto Alcantara Gomes, Rio de Janeiro State University (UERJ), Rio de Janeiro, Brazil.
Front Immunol. 2023 Jan 24;14:1075834. doi: 10.3389/fimmu.2023.1075834. eCollection 2023.
The inflammasomes are intracellular multimeric protein complexes consisting of an innate immune sensor, the adapter protein ASC and the inflammatory caspases-1 and/or -11 and are important for the host defense against pathogens. Activaton of the receptor leads to formation of the inflammasomes and subsequent processing and activation of caspase-1 that cleaves the proinflammatory cytokines IL-1β and IL-18. Active caspase-1, and in some instances caspase-11, cleaves gasdermin D that translocates to the cell membrane where it forms pores resulting in the cell death program called pyroptosis. Inflammasomes can detect a range of microbial ligands through direct interaction or indirectly through diverse cellular processes including changes in ion fluxes, production of reactive oxygen species and disruption of various host cell functions. In this review, we will focus on the NLRP3, NLRP6, NLRC4 and AIM2 inflammasomes and how they are activated and regulated during infections with Gram-positive bacteria, including spp., spp. and .
炎症小体是一种细胞内多聚体蛋白复合物,由先天免疫传感器、衔接蛋白 ASC 和炎症性半胱天冬酶-1 和/或 -11 组成,对于宿主防御病原体至关重要。受体的激活导致炎症小体的形成,随后半胱天冬酶-1 的加工和激活,切割前炎症细胞因子 IL-1β 和 IL-18。活性半胱天冬酶-1,在某些情况下是半胱天冬酶-11,切割出向细胞膜易位的 gasdermin D,在那里形成孔,导致称为细胞焦亡的细胞死亡程序。炎症小体可以通过直接相互作用或通过多种细胞过程(包括离子通量变化、活性氧物质产生和各种宿主细胞功能障碍)检测到一系列微生物配体。在本综述中,我们将重点介绍 NLRP3、NLRP6、NLRC4 和 AIM2 炎症小体,以及它们在与革兰氏阳性细菌(包括 spp.、 spp. 和 )感染时的激活和调节方式。