Saito Megumu K
Center for iPS Cell Research and Application, Kyoto University, Kyoto, Japan.
Nihon Rinsho Meneki Gakkai Kaishi. 2011;34(1):20-8. doi: 10.2177/jsci.34.20.
Although inflammation is important for host defense, excessive inflammation sometimes causes serious consequences. IL-1β is one of major proinflammatory cytokines. Dysregulation of IL-1β promotes development of several diseases. Mature IL-1β is produced by cleavage of its proform by a protein complex named inflammasome. Inflammasome consists of NOD-LRRs containing family (NLR proteins), an adaptor protein, and a cysteine protease caspase-1. Several NLRs can be assembled into inflammasome in response to various stimulatory signals. Genetic disorder of inflammasome-IL-1 system cause autoinflammatory diseases such as cryopyrin-associated autoinflammatory disease, familial Mediterranean fever, deficiency of IL-1 receptor antagonist, and PAPA syndrome. This article reviews recent advances in the study of inflammasome and related diseases.
尽管炎症对宿主防御很重要,但过度炎症有时会导致严重后果。白细胞介素-1β(IL-1β)是主要的促炎细胞因子之一。IL-1β的失调会促进多种疾病的发展。成熟的IL-1β是由一种名为炎性小体的蛋白质复合物切割其前体而产生的。炎性小体由含核苷酸结合寡聚化结构域样受体(NLR)家族蛋白(NLR蛋白)、一种接头蛋白和半胱氨酸蛋白酶caspase-1组成。几种NLR可响应各种刺激信号组装成炎性小体。炎性小体-IL-1系统的遗传紊乱会导致自身炎症性疾病,如冷吡啉相关的自身炎症性疾病、家族性地中海热、IL-1受体拮抗剂缺乏症和PAPA综合征。本文综述了炎性小体及相关疾病研究的最新进展。