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血小板反应蛋白-1与年龄相关性黄斑变性的发病机制

Thrombospondin-1 and Pathogenesis of Age-Related Macular Degeneration.

作者信息

Housset Michael, Sennlaub Florian

机构信息

1 Sorbonne Universités , UPMC Univ Paris 06, UMR_S 968, Institut de la Vision, Paris, France .

2 CNRS , UMR_7210, Paris, France .

出版信息

J Ocul Pharmacol Ther. 2015 Sep;31(7):406-12. doi: 10.1089/jop.2015.0023. Epub 2015 May 18.

Abstract

The cardinal features of age-related macular degeneration (AMD) are the accumulation of subretinal debris, subretinal inflammation, neovascularization, and degeneration of the photoreceptors and retinal pigment epithelium (RPE). Thrombospondin-1 (TSP-1) is a major matricellular protein that is physiologically expressed in the RPE and choroid, but severely diminished in eyes with AMD. TSP-1 plays an important role in phagocytosis, potently inhibits neovascularization, and mediates immune suppression and immune privilege. The lack of TSP-1 could have a central role in the pathogenesis of AMD as it is implicated in the major pathways that seem to be deficient in the disease. We here give an overview of the major functions of TSP-1 and how it could intervene in AMD pathogenesis.

摘要

年龄相关性黄斑变性(AMD)的主要特征是视网膜下碎片堆积、视网膜下炎症、新生血管形成以及光感受器和视网膜色素上皮(RPE)变性。血小板反应蛋白-1(TSP-1)是一种主要的基质细胞蛋白,在RPE和脉络膜中生理性表达,但在AMD患者眼中显著减少。TSP-1在吞噬作用中起重要作用,能有效抑制新生血管形成,并介导免疫抑制和免疫赦免。TSP-1的缺乏可能在AMD的发病机制中起核心作用,因为它涉及到该疾病中似乎存在缺陷的主要途径。我们在此概述TSP-1的主要功能以及它如何干预AMD的发病机制。

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