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冯俊侨, 杨柳, 周圆, 祁冰洁, 尹悦, 马乐, 张玮. 视网膜色素上皮氧化损伤SIRT1表达改变[J]. 中国公共卫生, 2018, 34(12): 1650-1653. DOI: 10.11847/zgggws1119547
引用本文: 冯俊侨, 杨柳, 周圆, 祁冰洁, 尹悦, 马乐, 张玮. 视网膜色素上皮氧化损伤SIRT1表达改变[J]. 中国公共卫生, 2018, 34(12): 1650-1653. DOI: 10.11847/zgggws1119547
Jun-qiao FENG, Liu YANG, Yuan ZHOU, . Oxidative stress-related discrepant expression of sirtuin 1 in human retinal pigment epithelial cells[J]. Chinese Journal of Public Health, 2018, 34(12): 1650-1653. DOI: 10.11847/zgggws1119547
Citation: Jun-qiao FENG, Liu YANG, Yuan ZHOU, . Oxidative stress-related discrepant expression of sirtuin 1 in human retinal pigment epithelial cells[J]. Chinese Journal of Public Health, 2018, 34(12): 1650-1653. DOI: 10.11847/zgggws1119547

视网膜色素上皮氧化损伤SIRT1表达改变

Oxidative stress-related discrepant expression of sirtuin 1 in human retinal pigment epithelial cells

  • 摘要:
      目的  明确氧化应激对视网膜色素上皮细胞(RPE)中去乙酰化酶1(SIRT1)表达的影响。
      方法  以人RPE细胞为实验对象,不同浓度H2O2(0、200、300 µmol/L)处理RPE细胞,观察处理后24 h细胞形态的改变情况,检测处理后24 h与72 h细胞中SIRT1的mRNA与蛋白表达情况。
      结果  H2O2作用后,随H2O2浓度的增加,RPE细胞的形态受损,有凋亡小体的出现;在氧化应激24 h后细胞内SIRT1的转录水平增加,而在氧化应激72 h后SIRT1的蛋白表达显著下降。
      结论  氧化应激可导致RPE细胞形态改变,SIRT1在RPE细胞内维持着氧化与抗氧化应激系统平衡,因此将SIRT1可作为临床上年龄相关性黄斑变性病(AMD)治疗的靶点。

     

    Abstract:
      Objective  To explore the effect of oxidative stress on sirtuin 1 (SIRT1) expression in retinal pigment epithelial (RPE) cells.
      Methods  Human RPE cells were treated with hydrogen peroxide (H2O2) at concentrations of 0, 200, 300 µmol/L. RPE cell morphology was observed with Giemsa staining 24 hours after the treatment. SIRT1 mRNA and protein expression were detected 24 and 72 hours after H2O2 treatment.
      Results  The morphology of RPE cells was damaged and apoptotic bodies were observed after treatment with different concentrations of H2O2; SIRT1 mRNA level was increased in a dose-dependent manner 24 hours after H2O2-induced oxidative stress. However, 72 hours after H2O2 treatment SIRT1 protein expression was reduced significantly.
      Conclusion  Oxidative stress can lead to morphological changes in RPE cells; SIRT1 maintains the balance of the oxidation reduction system in RPE cells and could be used as a therapeutic target in for clinical management of age-related macular degeneration (AMD).

     

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