van Dijk H, de Vos Burchart H, van Leeuwen M, Willers J M
Immunol Lett. 1986 Jun;12(5-6):281-8. doi: 10.1016/0165-2478(86)90031-3.
A new type of activation of the terminal route of complement is described. It occurs in precipitates of mouse serum prepared with a critical amount of polyethylene glycol. The activation proceeds in the presence of 10 mM EDTA and in the absence of C1q and functional C2, C3, C4 and factor B, which suggests that it is classical and alternative pathway-independent. The activation is demonstrated by the generation of both thermo-labile haemolytic and thermo-stable chemotactic activity. For both activities C5 seems to be essential. The haemolytic activity does not show species restriction towards sheep erythrocytes, which suggests a similarity with C56-initiated (reactive) but not with (S)C5-9-mediated (deviated) haemolysis. The identity of the haemolytic complex and the chemoattractant and the possible use of the new activation for the functional analysis of the mouse terminal complement route will be the subject of further study.
本文描述了一种补体终末途径的新型激活方式。它发生在用临界量聚乙二醇制备的小鼠血清沉淀物中。该激活过程在10 mM乙二胺四乙酸(EDTA)存在下进行,且不存在C1q以及功能性C2、C3、C4和B因子,这表明它不依赖经典途径和替代途径。热不稳定溶血活性和热稳定趋化活性的产生证明了这种激活。对于这两种活性,C5似乎至关重要。溶血活性对绵羊红细胞没有种属限制,这表明它与C56起始的(反应性)溶血相似,但与(S)C5 - 9介导的(偏离性)溶血不同。溶血复合物和趋化因子的同一性以及这种新激活方式在小鼠补体终末途径功能分析中的可能应用将是进一步研究的主题。