死孢子体1
脂褐素
视网膜色素上皮
生物
自噬
发病机制
细胞生物学
脉络膜新生血管
氧化应激
地理萎缩
炎症
黄斑变性
德鲁森
病理
视网膜
免疫学
医学
神经科学
视网膜
内分泌学
遗传学
细胞凋亡
眼科
生物化学
作者
Kai Kaarniranta,Janusz Błasiak,Paloma B. Liton,Michael E. Boulton,Daniel J. Klionsky,Debasish Sinha
出处
期刊:Autophagy
[Taylor & Francis]
日期:2022-04-25
卷期号:19 (2): 388-400
被引量:126
标识
DOI:10.1080/15548627.2022.2069437
摘要
Age-related macular degeneration (AMD) is the leading cause of visual impairment in the aging population with limited understanding of its pathogenesis and a lack of effective treatment. The progression of AMD is initially characterized by atrophic alterations in the retinal pigment epithelium, as well as the formation of lysosomal lipofuscin and extracellular drusen deposits. Damage caused by chronic oxidative stress, protein aggregation and inflammatory processes may lead to geographic atrophy and/or choroidal neovascularization and fibrosis. The role of macroautophagy/autophagy in AMD pathology is steadily emerging. This review describes selective and secretory autophagy and their role in drusen biogenesis, senescence-associated secretory phenotype, inflammation and epithelial-mesenchymal transition in the pathogenesis of AMD.
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