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Role of nuclear factor (erythroid-derived 2)-like 2 in the age-resistant properties of the glaucoma trabecular meshwork

机译:核因子(红细胞衍生的2)的作用 - 静电2在青光眼的抗性性能中

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摘要

Glaucoma is a major cause of irreversible blindness. Nuclear factor (erythroid-derived 2)-like 2 (Nrf2) regulates the expression of numerous antioxidants within cells and is therefore a focus of current ophthalmic research. To determine the roles of Nrf2 in mediating the glaucoma trabecular meshwork (GTM), the present study evaluated the levels of Nrf2 expression in GTM and human trabecular meshwork (HTM) cells by reverse-transcription-quantitative polymerase chain reaction and western blot analysis. It was principally observed that Nrf2 expression was downregulated in GTM cells. In addition, to determine the influence of Nrf2 on the apoptosis and proliferation of GTM and HTM cells, transfection assays and western blotting were performed to evaluate the expression of apoptosis-related proteins. The results of the current study indicated that Nrf2 may promote viability and reduce apoptosis in GTM and HTM cells. Collectively, these data suggest that Nrf2 may be a novel therapeutic target to treat glaucoma.
机译:青光眼是不可逆转的失明的主要原因。核因子(红细胞衍生的2) - 麦克风2(NRF2)调节细胞内无数抗氧化剂的表达,因此是目前眼科研究的重点。为了确定NRF2的角色在介导青光眼培养的网眼(GTM)中,本研究通过反转转录定量聚合酶链反应和Western印迹分析评估了GTM和人小梁杂交(HTM)细胞中NRF2表达的水平。主要观察到NRF2表达在GTM细胞中下调。此外,为了确定NRF2对GTM和HTM细胞的凋亡和增殖的影响,进行转染测定和蛋白质印迹,评价凋亡相关蛋白的表达。目前研究的结果表明,NRF2可以促进生存能力并降低GTM和HTM细胞中的细胞凋亡。总的来说,这些数据表明NRF2可以是治疗青光眼的新型治疗靶标。

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