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衰老视网膜色素上皮细胞中20S蛋白酶体活性及细胞内分布的改变

Alterations of activity and intracellular distribution of the 20S proteasome in ageing retinal pigment epithelial cells.

作者信息

Li Yue, Wang Yu-Sheng, Shen Xue-Feng, Hui Yan-Nian, Han Jing, Zhao Wei, Zhu Jie

机构信息

Department of Ophthalmology, Xijing Hospital, The Fourth Military Medical University and Eye Institute of PLA, Chang-le Road 17, Xi'an, Shaanxi 710032, China.

出版信息

Exp Gerontol. 2008 Dec;43(12):1114-22. doi: 10.1016/j.exger.2008.08.052. Epub 2008 Sep 13.

Abstract

Age-related macular degeneration (AMD) remains high incidence and accounts for a main cause of blindness in ageing people, but its mechanism is still poorly understood. Ageing and associated dysfunction of retinal pigment epithelial (RPE) cells were believed to be the pathological onset of AMD. 20S proteasome has been tightly correlated with cell ageing due to its fundamental role in maintaining cellular homeostasis, but its implication in the ageing process of human RPE cells was seldom concerned. This study aimed to demonstrate the interconnections between 20S proteasome and ageing RPE cells by characterizing age-dependent alterations of the 20S proteasome in primarily cultured human RPE cells. For this purpose, a replicative ageing RPE cell model was established and validated through testing the cell viability, beta-galactosidase activity and cellular autofluorescence. Decline in chymotrypsin-like, peptidylglutamyl-peptide hydrolase and trypsin-like activities of the 20S proteasome was detected in aged RPE cells through degradation of fluorogenic substrates. Immunofluorescence assay revealed that the 20S proteasome was concentrated in RPE nucleus, and redistributed partly to the peri-nuclear regions in old RPE passages. These age-dependent changes of the 20S complex were accompanied with a significantly increased fluorescent intensity of intracellular oxidized proteins. Further analysis of the proteasome-to-oxidized protein ratio indicated a preferred protection of the RPE nuclear proteins by the 20S proteasome, which also subsided remarkably as a function of the cell ageing. In conclusion, we demonstrated functional impairment and redistribution of the 20S proteasome with age in human RPE cells and supposed these alterations impactful on the process of RPE cell ageing and furthermore on the pathogenesis of AMD. Future researches on the mechanism of these alterations and the pathways to manipulate their effects are still strongly recommended.

摘要

年龄相关性黄斑变性(AMD)仍然具有高发病率,是老年人失明的主要原因之一,但其发病机制仍未完全明确。视网膜色素上皮(RPE)细胞的衰老及相关功能障碍被认为是AMD的病理起始因素。20S蛋白酶体因其在维持细胞内稳态中的重要作用而与细胞衰老密切相关,但它在人RPE细胞衰老过程中的作用却很少受到关注。本研究旨在通过对原代培养的人RPE细胞中20S蛋白酶体的年龄依赖性变化进行表征,来揭示20S蛋白酶体与衰老RPE细胞之间的内在联系。为此,通过检测细胞活力、β-半乳糖苷酶活性和细胞自发荧光,建立并验证了一种复制性衰老RPE细胞模型。通过荧光底物降解实验,检测到衰老RPE细胞中20S蛋白酶体的胰凝乳蛋白酶样、肽基谷氨酰肽水解酶和胰蛋白酶样活性下降。免疫荧光分析显示,20S蛋白酶体集中在RPE细胞核中,在衰老的RPE传代细胞中部分重新分布到核周区域。20S复合物这些年龄依赖性变化伴随着细胞内氧化蛋白荧光强度的显著增加。对蛋白酶体与氧化蛋白比率的进一步分析表明,20S蛋白酶体对RPE核蛋白具有优先保护作用,并且这种保护作用也随着细胞衰老而显著减弱。总之,我们证明了人RPE细胞中20S蛋白酶体随年龄增长出现功能损伤和重新分布,并推测这些改变对RPE细胞衰老过程进而对AMD的发病机制具有影响。强烈建议未来对这些改变的机制以及调控其作用途径进行研究。

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