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Oxidative stress and autophagy-related changes during retinal degeneration and development

机译:视网膜变性和发育过程中的氧化应激和自噬相关变化

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Retinitis pigmentosa (RP) is an inherited retinopathy that leads to photoreceptor loss. RP has been related to oxidative stress, autophagy, and inflammation. This study aimed to identify changes in the levels of oxidative stress and autophagy markers in the retina of control and rd10 mice during different phases of retinal development. Changes in the retinal oxidation system were investigated by measuring the levels of oxidized and reduced glutathione (GSH/GSSG), retinal avidin-positive cells, and 4-hydroxynonenal (4-HNE) staining intensity. Autophagy characterization was explored by measuring the levels of microtubule-associated protein 1 light chain 3 (LC3), beclin, autophagy-related proteins 5 and 7 (Atg5 and Atg7), and lysosomal associated membrane protein-2A (LAMP-2A). At P28 retinal GSH concentrations decreased in rd10 mice compared to the controls. No differences were found in retinal GSSG concentrations between the control and rd10 mice. There was an increase in retinal GSSG concentrations and a decrease in the GSH/GSSG ratio in the control and rd10 mice at P21 and P28 compared to P13. We observed an increase in avidin-positive cells in rd10 retinas. 4-HNE was increased in rd10 retinas at P13, and it also increased in control mice with age. We did not observe any differences in the retinal levels of LC3II/I ratio, Beclin, Atg5, or Atg7 in the rd10 mice compared to the controls. There was an increase in the LAMP-2A concentrations in the control and rd10 mice with development age (P28 concentrations vs. P13). Although only slight differences were found in the oxidative stress and autophagy markers between the control and rd10 mice, there were increases in the GSSG, 4-HNE, and LAMP-2A with age. This increase in the oxidative stress and chaperone-mediated autophagy has not been described before and occurred just after the mice opened their eyes, potentially indicating a retinal response to light exposure.
机译:色素性视网膜炎(RP)是一种遗传性视网膜病,可导致光感受器丧失。 RP与氧化应激,自噬和炎症有关。这项研究旨在确定在视网膜发育不同阶段,对照组和rd10小鼠视网膜中氧化应激和自噬标记物水平的变化。通过测量氧化和还原型谷胱甘肽(GSH / GSSG),视网膜亲和素阳性细胞和4-羟壬烯醛(4-HNE)染色强度的水平来研究视网膜氧化系统的变化。通过测量微管相关蛋白1轻链3(LC3),beclin,自噬相关蛋白5和7(Atg5和Atg7)以及溶酶体相关膜蛋白2A(LAMP-2A)的水平来探索自噬表征。与对照组相比,在P28时,rd10小鼠的视网膜GSH浓度降低。对照组和rd10小鼠之间的视网膜GSSG浓度未发现差异。与P13相比,在P21和P28的对照组和rd10小鼠的视网膜GSSG浓度增加,而GSH / GSSG比率降低。我们观察到rd10视网膜中抗生物素蛋白阳性细胞的增加。 4-HNE在P13的rd10视网膜中增加,并且在同龄小鼠中也增加。与对照组相比,我们在rd10小鼠中未观察到LC3II / I比,Beclin,Atg5或Atg7的视网膜水平有任何差异。对照和rd10小鼠的LAMP-2A浓度随发育年龄的增加而增加(P28浓度对P13)。尽管在对照组和rd10小鼠之间的氧化应激和自噬标记只有很小的差异,但是GSSG,4-HNE和LAMP-2A随年龄增加而增加。氧化应激和伴侣介导的自噬的这种增加在小鼠睁开眼睛之前并没有描述过,并且仅在小鼠睁开眼睛后才发生,这可能表明视网膜对光照的反应。

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