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RESEARCH PAPER / 2024-09-01

Senescent endothelial cells: a potential target for diabetic retinopathy.

Ying-Lu Liao, Yi-Fan Fang, Jia-Xing Sun, Guo-Rui Dou

Department of Ophthalmology, Eye Institute of Chinese PLA, Xijing Hospital, Fourth Military Medical University, Xi'an, 710032, China.Department of Ophthalmology, Eye Institute of Chinese PLA, Xijing Hospital, Fourth Military Medical University, Xi'an, 710032, China. · pubmed

Abstract

Diabetic retinopathy (DR) is a diabetic complication that results in visual impairment and relevant retinal diseases. Current therapeutic strategies on DR primarily focus on antiangiogenic therapies, which particularly target vascular endothelial growth factor and its related signaling transduction. However, these therapies still have limitations due to the intricate pathogenesis of DR. Emerging studies have shown that premature senescence of endothelial cells (ECs) in a hyperglycemic environment is involved in the disease process of DR and plays multiple roles at different stages. Moreover, these surprising discoveries have driven the development of senotherapeutics and strategies targeting senescent endothelial cells (SECs), which present challenging but promising prospects in DR treatment. In this review, we focus on the inducers and mechanisms of EC senescence in the pathogenesis of DR and summarize the current research advances in the development of senotherapeutics and strategies that target SECs for DR treatment. Herein, we highlight the role played by key factors at different stages of EC senescence, which will be critical for facilitating the development of future innovative treatment strategies that target the different stages of senescence in DR.

The following analysis is generated by AI and may contain errors. It is separate from the authors’ abstract and is not peer review.

Research summary

The paper discusses the role of senescent endothelial cells in the pathogenesis of diabetic retinopathy, which is related to aging processes. It explores potential therapeutic strategies targeting these senescent cells, indicating a focus on addressing underlying mechanisms rather than merely treating symptoms. However, while the findings are solid and contribute to the understanding of senescence in the context of an age-related disease, the impact is limited as it primarily reviews existing research rather than presenting novel experimental data or groundbreaking insights.

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