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细胞衰老与年龄相关性黄斑变性

刘威 龚莉莉

眼科学报2024,Vol.39Issue(7):332-344,13.
眼科学报2024,Vol.39Issue(7):332-344,13.DOI:10.12419/24071505

细胞衰老与年龄相关性黄斑变性

Cellular senescence in the pathogenesis of age-related macular degeneration

刘威 1龚莉莉1

作者信息

  • 1. 中山大学中山眼科中心,眼病防治全国重点实验室,广东省眼科视觉科学重点实验室,广州 510060
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摘要

Abstract

Age-related macular degeneration(AMD)is a leading cause of blindness among the elderly,characterized by the degeneration of retinal pigment epithelial cells and the death of photoreceptors.The pathogenesis of AMD is complex,involving a multitude of factors,including genetic,environmental,and metabolic influences.Cellular senescence serves as a significant risk factor for AMD,where cells enter a permanent state of cell cycle arrest after a limited number of divisions.As age increases,the accumulation of senescent cells is closely associated with various age-related chronic diseases.Key mechanisms underlying cellular senescence include oxidative stress,DNA damage,mitochondrial dysfunction,defects in autophagy and mitophagy,and epigenetic alterations.In the context of AMD,various cell types-including pigment epithelial cells,vascular endothelial cells,cells of Bruch's membrane,photoreceptors,and microglia-exhibit signs of senescence and related changes.Cellular senescence plays a pivotal role in the pathogenesis of AMD,contributing to the degeneration of different retinal cell types and supporting vascular systems.By thoroughly investigating these mechanisms,there is hope for the development of more effective therapies aimed at restoring and protecting vision in affected patients.This article reviews the biological mechanisms of cellular senescence and its role in AMD,exploring how different cell types contribute to the disease's onset,with the goal of providing new insights into the pathogenesis and treatment of AMD.

关键词

衰老/细胞衰老/年龄相关性黄斑变性/衰老相关分泌表型

Key words

aging/cellular senescence/age-related macular degeneration/senescence-associated secretory phenotype

分类

医药卫生

引用本文复制引用

刘威,龚莉莉..细胞衰老与年龄相关性黄斑变性[J].眼科学报,2024,39(7):332-344,13.

基金项目

广东省自然科学基金(2024A1515010518),广州市市校(院)企联合资助专题(2023A03J0184).This work was supported by the Natural Science Foundation of Guangdong Province(2024A1515010518)and Guangzhou Municipal-University(Institute)-Enterprise Jointly Funded Projects(2023A03J0184). (2024A1515010518)

眼科学报

1000-4432

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