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首页> 外文期刊>Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research >Photooxidative damage in retinal pigment epithelial cells via GRP78 and the protective role of grape skin polyphenols
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Photooxidative damage in retinal pigment epithelial cells via GRP78 and the protective role of grape skin polyphenols

机译:通过GRP78的视网膜颜料上皮细胞的光氧化损伤和葡萄皮肤多酚的保护作用

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Blue light induced oxidative damage and ER stress are related to the pathogenesis of age-related macular degeneration (AMD). However, the mechanism of blue light-induced damage remained obscure. The objective of this work is to assess the photooxidative damage to retinal pigment epithelial cells (RPE) and oxidation-induced changes in expression of ER stress associated apoptotic proteins, and investigate the mechanism underlying the protective effects of grape skin extracts. To mimic lipofuscin-mediated photooxidation in vivo, ARPE-19 cells that accumulated A2E, one of lipofuscin fluorophores, were used as a model system to investigate the mechanism of photooxidative damage and the protective effects of grape skin polyphenols. Exposure of A2E containing ARPE-19 cells to blue light resulted in significant apoptosis and increases in levels of GRP78, CHOP, p-JNK, Bax, cleaved caspase-9, and cleaved caspase-3, indicating that photooxidative damage to RPE cells is mediated by the ER-stress-induced intrinsic apoptotic pathway. Cells in which GRP78 had been knocked down with shRNA were more vulnerable to photooxidative damage. Pre-treatment of blue-light-exposed A2E containing ARPE-19 cells, with grape skin extracts, inhibited apoptosis, in a dose dependent manner. Knockdown GRP78 blocked the protective effect of grape skin extracts. (C) 2014 Elsevier Ltd. All rights reserved.
机译:蓝光诱导氧化损伤和ER应力与年龄相关性黄斑变性(AMD)的发病机制有关。然而,蓝光诱导损伤的机制仍然模糊不清。这项工作的目的是评估视网膜色素上皮细胞(RPE)的光氧化损伤,氧化诱导的ER应激相关凋亡蛋白表达的变化,并研究葡萄皮肤提取物的保护作用的基础。为了模仿脂血清蛋白介导的体内光氧化,累积A2e的ARPE-19细胞,脂肪植物蛋白荧光团中的一种,用作模型系统,以研究光氧化损伤的机制和葡萄皮肤多酚的保护作用。将A2E的暴露于ARPE-19细胞到蓝光导致显着的细胞凋亡,并且GRP78,CHOP,P-JNK,BAX,切割的caspase-9和切割的Caspase-3的水平增加,表明对RPE细胞的光氧化损伤是介导的通过Er-rency诱导的内在凋亡途径。将GRP78被ShRNA撞击的细胞更容易受到光氧化损伤的影响。预处理含有ARPE-19细胞的蓝色曝光A2E,葡萄皮肤提取物,抑制凋亡,以剂量依赖性方式抑制细胞凋亡。敲低GRP78阻止了葡萄皮肤提取物的保护作用。 (c)2014年elestvier有限公司保留所有权利。

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