The membrane attack complex as an inflammatory trigger

被引:142
作者
Morgan, B. Paul [1 ]
机构
[1] Cardiff Univ, Sch Med, Heath Pk, Cardiff CF14 4XN, S Glam, Wales
关键词
Complement; Membrane attack; Cell activation; PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA; COMPLEX/PERFORIN-LIKE PROTEINS; GLOMERULAR MESANGIAL CELLS; RAT THY-1 NEPHRITIS; NLRP3; INFLAMMASOME; PORE FORMATION; GPI-MICRODOMAINS; ACTIVATION; C5B-9; INJURY;
D O I
10.1016/j.imbio.2015.04.006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The final common pathway of all routes of complement activation involves the non-enzymatic assembly of a complex comprising newly formed C5b with the plasma proteins C6, C7, C8 and C9. When assembly occurs on a target cell membrane the forming complex inserts into and through the bilayer to create a pore, the membrane attack complex (MAC). On some targets, pore formation causes rapid lytic destruction; however, most nucleated cell targets resist lysis through a combination of ion pumps, membrane regulators and active recovery processes. Cells survive but not without consequence. The MAC pore causes ion fluxes and directly or indirectly impacts several important signalling pathways that in turn activate a diverse series of events in the cell, many of which are highly pro-inflammatory. Although this non-lytic, pro-inflammatory role of MAC has been recognised for thirty years, no consensus signalling pathway has emerged. Recent work, summarised here, has implicated specific signalling routes and, in some cells, inflammasome involvement, opening the door to novel approaches to therapy in complement-driven pathologies. (C) 2015 Elsevier GmbH. All rights reserved.
引用
收藏
页码:747 / 751
页数:5
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