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补体系统的末端复合物:新的结构见解及其与功能的相关性。

Terminal complexes of the complement system: new structural insights and their relevance to function.

机构信息

Systems Immunity Research Institute, Division of Infection and Immunity, School of Medicine, Cardiff University, Cardiff, UK.

Faculty of Natural Sciences, Department of Life Sciences, Imperial College, London, UK.

出版信息

Immunol Rev. 2016 Nov;274(1):141-151. doi: 10.1111/imr.12461.

Abstract

Complement is a key component of innate immunity in health and a powerful driver of inflammation and tissue injury in disease. The biological and pathological effects of complement activation are mediated by activation products. These come in two flavors: (i) proteolytic fragments of complement proteins (C3, C4, C5) generated during activation that bind specific receptors on target cells to mediate effects; (ii) the multimolecular membrane attack complex generated from the five terminal complement proteins that directly binds to and penetrates target cell membranes. Several recent publications have described structural insights that have changed perceptions of the nature of this membrane attack complex. This review will describe these recent advances in understanding of the structure of the membrane attack complex and its by-product the fluid-phase terminal complement complex and relate these new structural insights to functional consequences and cell responses to complement membrane attack.

摘要

补体是健康状态下固有免疫的关键组成部分,也是疾病中炎症和组织损伤的强大驱动因素。补体激活的生物学和病理学效应是由激活产物介导的。这些产物有两种形式:(i) 激活过程中产生的补体蛋白 (C3、C4、C5) 的蛋白水解片段,与靶细胞上的特定受体结合以介导效应;(ii) 从五个末端补体蛋白产生的多分子膜攻击复合物,直接与靶细胞膜结合并穿透。最近有几篇出版物描述了改变人们对这种膜攻击复合物性质的认识的结构见解。本综述将描述对膜攻击复合物及其副产物液相末端补体复合物结构的这些最新理解,并将这些新的结构见解与功能后果和细胞对补体膜攻击的反应联系起来。

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