视网膜视觉周期和lc3相关吞噬:调节机制和治疗潜力。

IF 7.5
Fanfei Liu, Qiqi Li, Yang Yang, Fang Lu
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引用次数: 0

摘要

视觉循环在视网膜中起着关键的双重作用,它通过光敏的11-顺式视网膜发色团的不断再生来维持视力。它的失调对视网膜退行性疾病包括年龄相关性黄斑变性(AMD)和Stargardt病有重要作用。最近的研究已经阐明了视觉周期的多个治疗靶点,从抑制RPE65和卵磷脂视黄醇酰基转移酶(LRAT)的酶活性到调节类视黄醇转运蛋白和增强lc3相关的保护性吞噬。视觉周期的药物干预在减少毒性类视黄醇积累方面显示出有希望的结果,尽管临床应用面临着包括夜盲症、延迟暗适应和色盲在内的挑战。未来的研究方向强调需要有针对性的视觉周期调节剂,可以选择性地破坏病理过程而不损害基本的视觉功能。本文综述了视觉周期和lc3相关吞噬与各种视网膜疾病的关系,重点介绍了视觉周期的药理调节的最新进展,旨在为视网膜退行性疾病的治疗策略提供新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Visual cycle and LC3-associated phagocytosis in retina: regulatory mechanisms and therapeutic potential.

The visual cycle plays a pivotal dual role in retina, while it's essential for maintaining vision through continuous regeneration of the light-sensitive 11-cis-retinal chromophore. Its dysregulation contributes significantly to retinal degenerative disorders including age-related macular degeneration (AMD) and Stargardt disease. Recent advances have elucidated multiple therapeutic targets in visual cycle, ranging from inhibition of enzymatic activity of RPE65 and lecithin retinol acyltransferase (LRAT) to modulation of retinoid transport proteins and enhancement of protective LC3-associated phagocytosis. Pharmacological interventions of the visual cycle demonstrate promising results in reducing toxic retinoid accumulation, though clinical application faces challenges including nyctalopia, delayed dark adaptation, and dyschromatopsia. Future research directions emphasize the need for targeted visual cycle modulators that can selectively disrupt pathological processes without compromising essential visual function. This review summarizes the visual cycle and LC3-associated phagocytosis associated with various retinal diseases, highlights recent advances in pharmacological modulation of visual cycle, and aims to provide new insights into therapeutic strategies for retinal degenerative disorders.

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