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炎症是如何引发的?白细胞介素-1、白细胞介素-18和高迁移率族蛋白B1的个体影响。

How is inflammation initiated? Individual influences of IL-1, IL-18 and HMGB1.

作者信息

Keyel Peter A

机构信息

Department of Biological Sciences, Texas Tech University, Biology Rm 108, Box 43131, Lubbock, TX 79409-3131, United States.

出版信息

Cytokine. 2014 Sep;69(1):136-45. doi: 10.1016/j.cyto.2014.03.007. Epub 2014 Apr 16.

Abstract

Pro-inflammatory cytokines are crucial for fighting infection and establishing immunity. Recently, other proteins, such as danger-associated molecular patterns (DAMPs), have also been appreciated for their role in inflammation and immunity. Following the formation and activation of multiprotein complexes, termed inflammasomes, two cytokines, IL-1β and IL-18, along with the DAMP High Mobility Group Box 1 (HMGB1), are released from cells. Although these proteins all lack classical secretion signals and are released by inflammasome activation, they each lead to different downstream consequences. This review examines how various inflammasomes promote the release of IL-1β, IL-18 and HMGB1 to combat pathogenic situations. Each of these effector molecules plays distinct roles during sterile inflammation, responding to viral, bacterial and parasite infection, and tailoring the innate immune response to specific threats.

摘要

促炎细胞因子对于对抗感染和建立免疫至关重要。最近,其他蛋白质,如危险相关分子模式(DAMPs),在炎症和免疫中的作用也得到了认可。在称为炎性小体的多蛋白复合物形成并激活后,两种细胞因子白细胞介素-1β(IL-1β)和白细胞介素-18(IL-18),以及DAMP高迁移率族蛋白B1(HMGB1)从细胞中释放出来。尽管这些蛋白质都缺乏经典的分泌信号,并且通过炎性小体激活而释放,但它们各自会导致不同的下游后果。本综述探讨了各种炎性小体如何促进IL-1β、IL-18和HMGB1的释放以应对致病情况。这些效应分子中的每一个在无菌性炎症、应对病毒、细菌和寄生虫感染以及针对特定威胁调整固有免疫反应过程中都发挥着独特作用。

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