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敲低 FOXO6 抑制高糖诱导的视网膜色素上皮细胞氧化应激和细胞凋亡。

Knockdown of FOXO6 inhibits high glucose-induced oxidative stress and apoptosis in retinal pigment epithelial cells.

机构信息

Department of Ophthalmology, Xi'an No. 4 Hospital, Guangren Hospital of Xi'an Jiaotong University, Xi'an, China.

Department of Endocrinology, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.

出版信息

J Cell Biochem. 2019 Jun;120(6):9716-9723. doi: 10.1002/jcb.28252. Epub 2018 Dec 12.

DOI:10.1002/jcb.28252
PMID:30548643
Abstract

Oxidative stress and apoptosis in retinal pigment epithelium cells are involved in the pathogenesis of diabetic retinopathy (DR). Forkhead box class O 6 (FOXO6) is a member of the FOXO family that can regulate diabetes-induced oxidative stress. However, the role of FOXO6 in DR has not been clarified. The aim of the present study was to investigate the effects of FOXO6 on high glucose (HG)-induced oxidative stress and apoptosis in ARPE-19 cells. The results showed that FOXO6 was overexpressed in clinical vitreous samples from DR patients and in HG-induced ARPE-19 cells. Knockdown of FOXO6 by small interfeing RNA targeting FOXO6 (si-FOXO6) mitigated the HG-induced the production of reactive oxygen species and malondialdehyde, as well as the inhibition of superoxide dismutase activity. Knockdown of FOXO6 reduced the rate of cell apoptosis in HG-induced ARPE-19 cells. The increase in bax expression and decrease in bcl-2 expression caused by HG stimulation were reversed by si-FOXO6 transfection. Furthermore, knockdown of FOXO6 enhanced the activation of Akt/Nrf2 pathway in HG-stimulated ARPE-19 cells. Taken together, suppression of FOXO6 protects ARPE-19 cells from HG-induced oxidative stress and apoptosis, which is in part mediated by the activation of Akt/Nrf2 pathway.

摘要

氧化应激和视网膜色素上皮细胞凋亡参与糖尿病性视网膜病变(DR)的发病机制。叉头框 O 类 6(FOXO6)是 FOXO 家族的一员,可调节糖尿病诱导的氧化应激。然而,FOXO6 在 DR 中的作用尚未阐明。本研究旨在探讨 FOXO6 对高葡萄糖(HG)诱导的 ARPE-19 细胞氧化应激和凋亡的影响。结果表明,DR 患者的临床玻璃体样本和 HG 诱导的 ARPE-19 细胞中过表达 FOXO6。靶向 FOXO6 的小干扰 RNA(si-FOXO6)敲低 FOXO6 减轻了 HG 诱导的活性氧和丙二醛的产生,以及超氧化物歧化酶活性的抑制。FOXO6 敲低减少了 HG 诱导的 ARPE-19 细胞中的细胞凋亡率。HG 刺激引起的 bax 表达增加和 bcl-2 表达减少被 si-FOXO6 转染逆转。此外,FOXO6 敲低增强了 HG 刺激的 ARPE-19 细胞中 Akt/Nrf2 通路的激活。综上所述,抑制 FOXO6 可保护 ARPE-19 细胞免受 HG 诱导的氧化应激和凋亡,部分是通过激活 Akt/Nrf2 通路介导的。

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