Program in Molecular Medicine, National Yang-Ming University and Academia Sinica, Taipei, Taiwan.
Neurobiol Dis. 2012 May;46(2):450-62. doi: 10.1016/j.nbd.2012.02.010. Epub 2012 Mar 3.
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.
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。