Jiang H, Burdick D, Glabe C G, Cotman C W, Tenner A J
Department of Molecular Biology and Biochemistry, University of California, Irvine 92717.
J Immunol. 1994 May 15;152(10):5050-9.
beta-amyloid peptides that accumulate within the brain of individuals with Alzheimer's disease bind to C1q and activate the classical C pathway via a specific interaction with a site within the collagen-like domain of C1q (C1q-CLF). Synthetic analogues of beta-amyloid peptides, beta 1-42 and beta 1-40, bound to C1q and were strong activators of C as assessed by both total C consumption and C4 consumption. beta 1-42 was significantly more effective than beta 1-40 in binding to C1q and triggering C activation, whereas beta 1-28 demonstrated little or no binding or C activation. This C-activating capacity seems to be largely correlated with the assembly of the beta 1-42 into low speed sedimentable aggregates and/or macromolecular fibrils. Radiolabeled C1q and C1q-CLF bind specifically to these aggregates or amyloid fibrils. In addition, using synthetic C1q peptides in a solid phase binding assay, the major binding site of beta 1-42 to C1q was localized to the C1q A chain collagen-like residues 14-26, a region previously described as a novel interaction site for Ab-independent activators of C1. C1q A chain peptide 14-26 blocked the ability of beta-amyloid peptides to activate the classical C pathway, providing evidence that this relatively unrecognized mechanism of C activation (via binding to the C1q-CLF) may have crucial physiologic consequences. Finally, these observations provide further support for the hypothesis that C activation and inflammation may be a component in the pathogenesis of AD and suggest possibilities for modulating the progression of AD.
在阿尔茨海默病患者大脑中积累的β-淀粉样肽与C1q结合,并通过与C1q胶原样结构域(C1q-CLF)内的一个位点的特异性相互作用激活经典补体途径。β-淀粉样肽的合成类似物β1-42和β1-40与C1q结合,并且通过总补体消耗和C4消耗评估,它们是补体的强激活剂。β1-42在结合C1q和触发补体激活方面比β1-40显著更有效,而β1-28显示出很少或没有结合或补体激活。这种补体激活能力似乎在很大程度上与β1-42组装成低速可沉淀聚集体和/或大分子纤维有关。放射性标记的C1q和C1q-CLF特异性结合这些聚集体或淀粉样纤维。此外,在固相结合试验中使用合成的C1q肽,β1-42与C1q的主要结合位点定位于C1q A链胶原样残基14-26,该区域先前被描述为C1的非抗体依赖性激活剂的新相互作用位点。C1q A链肽14-26阻断了β-淀粉样肽激活经典补体途径的能力,提供了证据表明这种相对未被认识的补体激活机制(通过与C1q-CLF结合)可能具有关键的生理后果。最后,这些观察结果为补体激活和炎症可能是AD发病机制的一个组成部分这一假设提供了进一步支持,并提示了调节AD进展的可能性。