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胱抑素C在黄斑和神经元变性中的作用:对年龄相关性黄斑变性机制的启示

Cystatin C in macular and neuronal degenerations: implications for mechanism(s) of age-related macular degeneration.

作者信息

Paraoan Luminita, Hiscott Paul, Gosden Christine, Grierson Ian

机构信息

Unit of Ophthalmology, School of Clinical Sciences, Liverpool L69 3GA, UK.

出版信息

Vision Res. 2010 Mar 31;50(7):737-42. doi: 10.1016/j.visres.2009.10.022. Epub 2009 Nov 14.

Abstract

Cystatin C is a strong inhibitor of cysteine proteinases expressed by diverse cells. Variant B cystatin C, which was associated with increased risk of developing age-related macular degeneration, differs from the wild type protein by a single amino acid (A25T) in the signal sequence responsible for its targeting to the secretory pathway. The same variant conveys susceptibility to Alzheimer disease. Our investigations of the trafficking and processing of variant B cystatin C in living RPE cells highlight impaired secretion of extracellular modulators and inappropriate protein retention in RPE cells as potential molecular mechanisms underpinning macular, and possibly neuronal, degeneration.

摘要

胱抑素C是一种由多种细胞表达的半胱氨酸蛋白酶的强效抑制剂。与年龄相关性黄斑变性发病风险增加相关的B型胱抑素C变体,与野生型蛋白在负责其靶向分泌途径的信号序列中有一个氨基酸不同(A25T)。相同的变体也使人易患阿尔茨海默病。我们对活的视网膜色素上皮(RPE)细胞中B型胱抑素C的运输和加工的研究强调,细胞外调节剂分泌受损以及RPE细胞中蛋白质保留不当是黄斑变性以及可能的神经元变性的潜在分子机制。

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