Targeting cullin 3 by miR-601 activates Nrf2 signaling to protect retinal pigment epithelium cells from hydrogen peroxide

被引:28
作者
Chen, Zhi-Jun [1 ,2 ]
Rong, Ling [1 ]
Huang, Dan [1 ]
Jiang, Qin [1 ]
机构
[1] Nanjing Med Univ, Affiliated Eye Hosp, Sch Clin Med 4, 138 Han Zhong Rd, Nanjing 210029, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Childrens Hosp, Dept Ophthalmol, Nanjing, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Retinal pigment epithelium cells; Oxidative injury; cullin; 3; Nrf2; miR-601; OXIDATIVE STRESS; BREAST-CANCER; GROWTH; SENSITIVITY; MECHANISMS; DAMAGE; KEAP1; CUL3;
D O I
10.1016/j.bbrc.2019.05.171
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Activation of Nrf2 cascade can protect retinal pigment epithelium (RPE) cells from hydrogen peroxide (H2O2) and other oxidative injury. The current study identified microRNA-601 (miR-601) as a novel cullin 3 (Cul3)-targeting miRNA that activates Nrf2 cascade. In ARPE-19 cells and primary human RPE cells, forced overexpression of miR-601 significantly inhibited Cul3 3'-UTR activity and downregulated Cul3 mRNA/protein expression, leading to Nrf2 protein stabilization and its nuclear translocation as well as expression of anti-oxidant response elements (ARE)-dependent genes (HO1, NQO1 and GCLC). H2O2 treatment increased miR-601 levels in RPE cells. Significantly, ectopic miR-601 overexpression attenuated H2O2-induced oxidative injury and apoptosis in RPE cells. In contrast, miR-601 inhibition promoted Cul3 expression, lowered basal Nrf2 activation, and enhanced H2O2-induced oxidative stress and apoptosis in RPE cells. In ARPE-19 cells, CRISPC/Cas9-mediated knockout (KO) of Cul3 or Keapl not only mimicked, but also nullified, miR-601-inudced anti-H2O2 actions. Furthermore, Nrf2 silencing by targeted shRNAs abolished miR-601-inudced cytoprotection in H2O2-treated ARPE-19 cells. Taken together, we show that miR-601 activates Nrf2 signaling to protect RPE cells from H2O2 by targeting Cul3. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:679 / 687
页数:9
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