MANF 通过 PI3K/AKT/GSK3β 通路对 6-OHDA 诱导的细胞损伤的 Nrf2 介导的神经保护作用。

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

机构信息

Department of Neurology, Shanghai Tongji Hospital, Tongji University School of Medicine, 389 Xincun Road, Shanghai 200065, PR China.

Biomedical Research Center, Tongji University Suzhou Institute, Building 2198 Jinfeng Road, Wuzhong District, Suzhou, Jiangsu 215101, PR China.

出版信息

Exp Gerontol. 2017 Dec 15;100:77-86. doi: 10.1016/j.exger.2017.10.021. Epub 2017 Oct 25.

Abstract

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 (GSK3β) activation. PI3K inhibitor (LY49002) abolished effects of MANF on AKT phosphorylation, GSK3β 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/GSK3β pathway.

摘要

氧化应激和细胞凋亡被认为广泛参与帕金森病的发病机制。我们之前报道过,脑星形胶质细胞衍生神经营养因子(MANF)具有抗氧化和抗凋亡作用,可以对抗 6-OHDA 诱导的神经毒性,但具体的分子机制尚不清楚。在这项研究中,我们表明 MANF 上调核因子红细胞 2 相关因子(Nrf2)的表达,并促进其向核内转位。Nrf2 的抑制剂或 shRNA 介导的敲低部分阻断了 MANF 的抗氧化和抗凋亡作用。此外,MANF 激活了磷酸肌醇 3-激酶(PI3K)/蛋白激酶 B(Akt)信号通路,并抑制了糖原合成酶激酶(GSK3β)的激活。PI3K 抑制剂(LY49002)消除了 MANF 对 AKT 磷酸化、GSK3β失活、Nrf2 核易位的影响,随后消除了 MANF 介导的细胞保护作用。综上所述,我们的研究结果表明,MANF 通过激活 PI3K/Akt/GSK3β 通路增强 Nrf2 相关生存机制,从而介导对抗 6-OHDA 诱导的细胞毒性的保护作用。

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