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补体系统在 AMD 中的作用。

The role of complement in AMD.

机构信息

Department of Infection Biology, Leibniz Institute for Natural Product Research and Infection Biology, Beutenbergstrasse 11a, Jena, Germany.

出版信息

Adv Exp Med Biol. 2010;703:9-24. doi: 10.1007/978-1-4419-5635-4_2.

Abstract

Age related macular degeneration (AMD) is a common form of blindness in the western world and genetic variations of several complement genes, including the complement regulator Factor H, the central complement component C3, Factor B, C2, and also Factor I confer a risk for the disease. However deletion of a chromosomal segment in the Factor H gene cluster on human chromosome 1, which results in the deficiency of the terminal pathway regulator CFHR1, and of the putative complement regulator CFHR3 has a protective effect for development of AMD. The Factor H gene encodes two proteins Factor H and FHL1 which are derived from alternatively processed transcripts. In particular a sequence variation at position 402 of both Factor H and FHL1 is associated with a risk for AMD. A tyrosine residue at position 402 represents the protective and a histidine residue the risk variant. AMD is considered a chronic inflammatory disease, which can be caused by defective and inappropriate regulation of the continuously activated alternative complement pathway. This activation generates complement effector products and inflammatory mediators that stimulate further inflammatory reactions. Defective regulation can lead to formation of immune deposits, drusen and ultimately translate into damage of retinal pigment epithelial cells, rupture of the interface between these epithelial cells and the Bruch's membrane and vision loss. Here we describe the role of complement in the retina and summarize the current concept how defective or inappropriate local complement control contributes to inflammation and the pathophysiology of AMD.

摘要

年龄相关性黄斑变性(AMD)是西方世界常见的失明形式,几种补体基因的遗传变异,包括补体调节剂因子 H、中心补体成分 C3、因子 B、C2,以及因子 I,都与疾病风险相关。然而,人类 1 号染色体上因子 H 基因簇中的一个染色体片段缺失,导致末端途径调节剂 CFHR1 和假定的补体调节剂 CFHR3 的缺乏,对 AMD 的发展具有保护作用。因子 H 基因编码两种蛋白因子 H 和 FHL1,它们来自于不同的加工转录本。特别是,因子 H 和 FHL1 在位置 402 的序列变异与 AMD 的风险相关。位置 402 的酪氨酸残基代表保护性变异,组氨酸残基代表风险变异。AMD 被认为是一种慢性炎症性疾病,可能是由于不断激活的替代补体途径的缺陷和不适当调节引起的。这种激活产生补体效应产物和炎症介质,刺激进一步的炎症反应。调节缺陷可导致免疫沉积物、玻璃膜疣的形成,最终转化为视网膜色素上皮细胞的损伤、这些上皮细胞与 Bruch 膜之间的界面破裂以及视力丧失。在这里,我们描述了补体在视网膜中的作用,并总结了当前关于局部补体控制缺陷或不适当如何导致炎症和 AMD 病理生理学的概念。

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