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细胞内补体激活——一种警报引发机制?

Intracellular complement activation-An alarm raising mechanism?

机构信息

Sir William Dunn School of Pathology, University of Oxford, Oxford, United Kingdom.

Department of Bacteriology and Immunology, Haartman Institute, Immunobiology Research Program, University of Helsinki, Helsinki, Finland; Helsinki University Central Hospital Laboratory (HUSLAB), Helsinki, Finland.

出版信息

Semin Immunol. 2018 Aug;38:54-62. doi: 10.1016/j.smim.2018.03.003. Epub 2018 Apr 7.

Abstract

It has become increasingly apparent that the complement system, being an ancient defense mechanism, is not operative only in the extracellular milieu but also intracellularly. In addition to the known synthetic machinery in the liver and by macrophages, many other cell types, including lymphocytes, adipocytes and epithelial cells produce selected complement components. Activation of e.g. C3 and C5 inside cells may have multiple effects ranging from direct antimicrobial defense to cell differentiation and possible influence on metabolism. Intracellular activation of C3 and C5 in T cells is involved in the maintenance of immunological tolerance and promotes differentiation of T helper cells into Th1-type cells that activate cell-mediated immune responses. Adipocytes are unique in producing many complement sensor proteins (like C1q) and Factor D (adipsin), the key enzyme in promoting alternative pathway amplification. The effects of complement activation products are mediated by intracellular and cell membrane receptors, like C3aR, C5aR1, C5aR2 and the complement regulator MCP/CD46, often jointly with other receptors like the T cell receptor, Toll-like receptors and those of the inflammasomes. These recent observations link complement activation to cellular metabolic processes, intracellular defense reactions and to diverse adaptive immune responses. The complement components may thus be viewed as intracellular alarm molecules involved in the cellular danger response.

摘要

越来越明显的是,补体系统作为一种古老的防御机制,不仅在细胞外环境中起作用,而且在细胞内也起作用。除了肝脏和巨噬细胞中已知的合成机制外,许多其他细胞类型,包括淋巴细胞、脂肪细胞和上皮细胞,也会产生选定的补体成分。例如,C3 和 C5 在细胞内的激活可能具有多种效应,从直接的抗菌防御到细胞分化,以及对代谢的可能影响。T 细胞内 C3 和 C5 的激活参与了免疫耐受的维持,并促进辅助性 T 细胞向 Th1 型细胞的分化,从而激活细胞介导的免疫反应。脂肪细胞在产生许多补体传感器蛋白(如 C1q)和因子 D(脂联素)方面是独特的,因子 D 是促进替代途径放大的关键酶。补体激活产物的作用是通过细胞内和细胞膜受体介导的,如 C3aR、C5aR1、C5aR2 和补体调节剂 MCP/CD46,通常与其他受体(如 T 细胞受体、Toll 样受体和炎症小体受体)共同作用。这些最近的观察结果将补体激活与细胞代谢过程、细胞内防御反应和多种适应性免疫反应联系起来。因此,补体成分可以被视为参与细胞危险反应的细胞内警报分子。

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