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c-Jun 依赖性硫氧还蛋白诱导介导脑源性神经营养因子对大鼠皮质神经元线粒体抑制的保护作用。

c-Jun-dependent sulfiredoxin induction mediates BDNF protection against mitochondrial inhibition in rat cortical neurons.

机构信息

Program in Molecular Medicine, National Yang-Ming University and Academia Sinica, Taipei, Taiwan.

出版信息

Neurobiol Dis. 2012 May;46(2):450-62. doi: 10.1016/j.nbd.2012.02.010. Epub 2012 Mar 3.

Abstract

In current study, we tested the hypothesis that c-Jun-dependent sulfiredoxin expression mediates protective effects of brain-derived neurotrophic factor (BDNF) against neurotoxicity induced by 3-nitropropionic acid (3-NP), a mitochondrial complex II inhibitor, in primary rat cortical cultures. We found that BDNF-dependent c-Jun expression and nuclear translocation required prior phosphorylation of extracellular signal-regulated kinase (ERK)1/2, but not Akt. BDNF also transiently activated the expression of sulfiredoxin, an ATP-dependent antioxidant enzyme, at both mRNA and protein levels. Furthermore, both c-Jun siRNA and ERK1/2 inhibitor PD98059 suppressed BDNF-induced sulfiredoxin expression. Finally, PD98059, c-Jun siRNA, and sulfiredoxin siRNA all abrogated BDNF-mediated 3-NP resistance. Together, these results established a signaling cascade of "BDNF → ERK1/2-Pi → c-Jun → sulfiredoxin → 3-NP resistance". We therefore conclude that c-Jun-induced sulfiredoxin mediates the BDNF-dependent neuroprotective effects against 3-NP toxicity in primary rat cortical neurons, at least in part.

摘要

在本研究中,我们验证了这样一个假设,即 c-Jun 依赖性硫氧还蛋白表达介导了脑源性神经营养因子 (BDNF) 对 3-硝基丙酸 (3-NP) 诱导的神经毒性的保护作用,3-NP 是一种线粒体复合物 II 抑制剂,在原代大鼠皮质培养物中。我们发现,BDNF 依赖性 c-Jun 表达和核易位需要细胞外信号调节激酶 (ERK)1/2 的磷酸化,但不需要 Akt。BDNF 还可瞬时激活硫氧还蛋白的表达,一种依赖 ATP 的抗氧化酶,在 mRNA 和蛋白质水平上。此外,c-Jun siRNA 和 ERK1/2 抑制剂 PD98059 均抑制 BDNF 诱导的硫氧还蛋白表达。最后,PD98059、c-Jun siRNA 和硫氧还蛋白 siRNA 均消除了 BDNF 介导的 3-NP 抗性。总之,这些结果确立了“BDNF→ERK1/2-Pi→c-Jun→硫氧还蛋白→3-NP 抗性”的信号级联。因此,我们得出结论,c-Jun 诱导的硫氧还蛋白介导了 BDNF 对原代大鼠皮质神经元中 3-NP 毒性的依赖作用,至少部分如此。

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