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首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Overoxidation of peroxiredoxins in vivo in cultured human umbilical vein endothelial cells and in damaging light-exposed mouse retinal tissues.
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Overoxidation of peroxiredoxins in vivo in cultured human umbilical vein endothelial cells and in damaging light-exposed mouse retinal tissues.

机译:在培养的人脐静脉内皮细胞中和在受损的轻度暴露的小鼠视网膜组织中,过氧化物酶的体内过氧化作用。

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摘要

Reduced and overoxidized forms of peroxiredoxins (Prxs) in vivo were assessed in cultured human umbilical vein endothelial cells (HUVEC) and in damaging light-exposed mouse retinal tissues by two-dimensional (2D) gel electrophoresis and Western blot analysis. Acidic isoelectric point (pI) shift of protein spots of Prx2, 3, 4, and 6, which indicate formation of overoxidized Prx was clearly observed after treatment with H(2)O(2) but was not observed after treatment with the radical initiators 2,2'-azobis (2-amidinopropane) dihydrochloride (AAPH) and 2,2'-azobis [2-(2-imidazolin-2-yl)propane] dihydrochloride (AIPH); this finding indicated selective oxidation of Prx molecules by H(2)O(2). Following the exposure of the eyes of mice to visible light (5000lx) for up to 4h, no acidic spot shift was observed in Prx1, 2, and 6 in both retinal and retinal pigment epithelial samples; this finding indicated the possible involvement of the photosensitization reaction rather than free radicals derived from H(2)O(2) in this pathology. Detection of overoxidized Prxs may be applicable for assessing the mechanisms of cell/tissue damage caused by oxidative stress in vivo.
机译:通过二维(2D)凝胶电泳和Western印迹分析,在培养的人脐静脉内皮细胞(HUVEC)和在受损的轻度暴露的小鼠视网膜组织中评估了体内过氧化物和过氧化物的还原和过氧化形式。 Prx2、3、4和6的蛋白质斑点的酸性等电点(pI)位移表明过氧化的Prx的形成在用H(2)O(2)处理后可以清楚地观察到,但是在用自由基引发剂处理后却没有观察到2,2′-偶氮二(2-prop基丙烷)二盐酸盐(AAPH)和2,2′-偶氮二[2-(2-咪唑啉-2-基)丙烷]二盐酸盐(AIPH);该发现表明H(2)O(2)对Prx分子的选择性氧化。在将小鼠的眼睛暴露于可见光(5000lx)下长达4h之后,在视网膜和视网膜色素上皮样品中Prx1、2和6中均未观察到酸性斑点的移动。这一发现表明这种光化反应的可能参与而不是源自H(2)O(2)的自由基。过氧化的Prx的检测可能适用于评估体内氧化应激引起的细胞/组织损伤的机制。

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