Nrf2-mediated neuroprotection by MANF against 6-OHDA-induced cell damage via PI3K/AKT/GSK3β pathway

被引:48
作者
Zhang, Jingxing [1 ]
Tong, Weifang [1 ]
Sun, Hui [1 ]
Jiang, Ming [3 ]
Shen, Yijue [1 ]
Liu, Yigang [1 ]
Gu, Hua [2 ]
Guo, Jia [3 ]
Fang, Jianmin [2 ,3 ]
Jin, Lingjing [1 ]
机构
[1] Tongji Univ, Sch Med, Shanghai Tongji Hosp, Dept Neurol, 389 Xincun Rd, Shanghai 200065, Peoples R China
[2] Tongji Univ, Sch Life Sci & Technol, 1239 Siping Rd, Shanghai 200092, Peoples R China
[3] Tongji Univ, Suzhou Inst, Biomed Res Ctr, Bldg 2198 Jinfeng Rd, Suzhou 215101, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
MANF; Nrf2; PI3K/Akt/GSK3; beta; Apoptosis; Oxidative stress; SH-SY5Y cells; NEUROTROPHIC FACTOR MANF; PARKINSONS-DISEASE; OXIDATIVE STRESS; NEURODEGENERATIVE DISEASES; SIGNALING PATHWAY; BRAIN-INJURY; RAT MODEL; NRF2; APOPTOSIS; PATHOGENESIS;
D O I
10.1016/j.exger.2017.10.021
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Oxidative stress and apoptosis are thought to be broadly involved in the pathogenesis of Parkinson's disease. We previously reported that Mesencephalic astrocyte-derived neurotrophic factor (MANF) possesses anti-oxidation and anti-apoptotic effects against 6-OHDA-induced neurotoxicity, but the specific molecular mechanism remains unclear. In this study, we showed that MANF up-regulates the expression of nuclear factor erythroid 2-related factor (Nrf2) and promotes its translocation into the nucleus. The anti-oxidation and anti-apoptotic effects of MANF could be partially blocked by inhibitor or shRNA-mediated knockdown of Nrf2. Furthermore, MANF activated phospoinositide-3-kinase (PI3K)/Akt signaling and suppressed glycogen synthase kinase (GSK3 beta) activation. PI3K inhibitor (LY49002) abolished effects of MANF on AKT phosphorylation, GSK3 beta inactivation, Nrf2 nuclear translocation and subsequently abrogated MANF-mediates cytoprotection. Collectively, our findings indicated that MANF-mediated protection against 6-OHDA-induced cytotoxicity by potentiating the Nrf2-related survival mechanism through the PI3K/Akt/GSK3 beta pathway.
引用
收藏
页码:77 / 86
页数:10
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