黄斑变性
发病机制
德鲁森
豁免特权
视网膜色素上皮
基质细胞蛋白
ABCA4型
脉络膜新生血管
血栓反应素
新生血管
医学
吞噬作用
脉络膜
脂褐素
血栓反应蛋白1
免疫系统
视网膜
生物
视网膜
免疫学
眼科
病理
血管生成
细胞生物学
癌症研究
神经科学
内科学
遗传学
细胞外基质
基因
基质金属蛋白酶
表型
金属蛋白酶
作者
Michael Housset,Florian Sennlaub
标识
DOI:10.1089/jop.2015.0023
摘要
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.
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