Division of Viral Infection, Department of Infectious Disease Control, International Research Center for Infectious Diseases, Institute of Medical Science, The University of Tokyo, Minato-ku, Tokyo 108-8639, Japan.
Division of Viral Infection, Department of Infectious Disease Control, International Research Center for Infectious Diseases, Institute of Medical Science, The University of Tokyo, Minato-ku, Tokyo 108-8639, Japan.
Trends Microbiol. 2015 Jan;23(1):55-63. doi: 10.1016/j.tim.2014.09.007. Epub 2014 Oct 22.
Inflammasomes are multiprotein complexes that induce downstream immune responses to specific pathogens, environmental stimuli, and host cell damage. Components of specific viruses activate different inflammasomes; for example, the influenza A virus M2 protein and encephalomyocarditis virus (EMCV) 2B protein activate the nucleotide-binding oligomerization domain (NOD)-like receptor family pyrin domain (PYD)-containing 3 (NLRP3) inflammasome, whereas viral double-stranded RNA (dsRNA) activates the retinoic acid inducible gene-I (RIG-I) inflammasome. Once activated in response to viral infection, inflammasomes induce the activation of caspases and the release of mature forms of interleukin-1β (IL-1β) and IL-18. Here we review the association between viral infection and inflammasome activation. Identifying the mechanisms underlying virus-induced inflammasome activation is important if we are to develop novel therapeutic strategies to target viruses.
炎症小体是一种多蛋白复合物,可诱导针对特定病原体、环境刺激物和宿主细胞损伤的下游免疫反应。特定病毒的成分激活不同的炎症小体;例如,甲型流感病毒 M2 蛋白和脑心肌炎病毒 (EMCV) 2B 蛋白激活核苷酸结合寡聚化结构域 (NOD)-样受体家族富含吡咯烷二酮 (PYD) 的 3 (NLRP3) 炎症小体,而病毒双链 RNA (dsRNA) 激活视黄酸诱导基因-I (RIG-I) 炎症小体。一旦对病毒感染作出反应而被激活,炎症小体就会诱导半胱天冬酶的激活以及白细胞介素-1β (IL-1β) 和白细胞介素-18 的成熟形式的释放。本文我们将综述病毒感染与炎症小体激活之间的关联。如果我们要开发针对病毒的新型治疗策略,那么确定病毒诱导的炎症小体激活的机制就非常重要。