激光生物学报摘要, 更新时间: 2007年4月29日
  由美国生科集团 (BVTech, Inc.) 主办
  
视紫红质及RPE65蛋白在光致视网膜变性疾病中的作用机制
激光生物学报摘要 2007-2

陈 鹏, 梁 洁, 钱焕文 (军事医学科学院放射与辐射医学研究所,北京 100850)

摘 要:视紫红质是感光细胞中的一种视色素,在光线的接收和视觉电位的产生方面具有重要的生理作用,由视紫红质介导的过度光信号传导是光性视网膜变性的主要原因。近年的研究表明,视网膜色素上皮细胞中的RPE65蛋白作为影响视紫红质再生的关键因素,与视网膜光损伤的易感性密切相关。就视紫红质和RPE65蛋白在光致视网膜变性中的作用机理作一探讨。


The Mechanism of Rhodopsin and RPE65 Protein in Light-induced Retina Degeneration

CHEN Peng,LIANG Jie,QIAN Huan-wen (Institute of Radiation Medicine, Academy of Military Medical Sciences, Beijing 100850, China)

Abstract:Light absorption by the visual pigment rhodopsin is required to initiate the phototransduction cascade. Absorption of excessive amount of light,however,may eventually lead to photoreceptor degeneretion by an apoptotic process.In some sense,light damage depends on the amount of rhodopsin available for bleaching during light exposure. The protein RPE65 is specifically expressed in the retinal pigment epithelium and essential for the re-isomerization of all-trans retinol in the visual cycle and thus for the regeneration of rhodopsin after bleaching. This article reviews the role of rhodopsin and RPE65 protein in retina light injury and other related retinitis pigmentosa degeneration disease.


 

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