Nicholson-Weller A, Halperin J A
Department of Medicine, Brigham and Women's Hospital, Boston, Mass.
Immunol Res. 1993;12(3):244-57. doi: 10.1007/BF02918256.
The terminal complement complexes C5b-7, C5b-8 and C5b-9 are able to generate nonlethal cell signals. One universal consequence of a cell being targeted by C5b-8 or C5b-9 is an influx of Ca2+. In addition, other second messengers, including cAMP, inositol phosphate intermediates and arachidonate metabolites, are generated by the terminal complement complexes in specific cell types. In vivo, terminal complement complexes have been found in a wide variety of inflammatory processes in humans and in experimental animal models. Some of these models of inflammation putatively induced by terminal complement complexes have been tested in complement-deficient animals, and indeed no inflammation results, which supports the critical role of the terminal complement complexes in the pathogenesis of the lesion.
终末补体复合物C5b-7、C5b-8和C5b-9能够产生非致死性细胞信号。细胞被C5b-8或C5b-9靶向作用的一个普遍结果是Ca2+内流。此外,终末补体复合物在特定细胞类型中还会产生其他第二信使,包括环磷酸腺苷(cAMP)、肌醇磷酸中间体和花生四烯酸代谢产物。在体内,已在人类多种炎症过程以及实验动物模型中发现了终末补体复合物。其中一些推测由终末补体复合物诱导的炎症模型已在补体缺陷动物中进行了测试,实际上并未引发炎症,这支持了终末补体复合物在病变发病机制中的关键作用。