Uittenbogaard Martine, Chiaramello Anne
Department of Anatomy and Cell Biology, George Washington University Medical Center, 2300 I Street NW, Washington, DC 20037, USA.
J Neurochem. 2005 Feb;92(3):585-96. doi: 10.1111/j.1471-4159.2004.02886.x.
The basic helix-loop-helix transcription factor Nex1/Math-2 belongs to the NeuroD subfamily, which plays a critical role during neuronal differentiation and maintenance of the differentiated state. Previously, we demonstrated that Nex1 is a key regulatory component of the nerve growth factor (NGF) pathway. Further supporting this hypothesis, this study shows that Nex1 has survival-inducing properties similar to NGF, as Nex1-overexpressing PC12 cells survive in the absence of trophic factors. We dissected the molecular mechanism by which Nex1 confers neuroprotection upon serum removal and found that constitutive expression of Nex1 maintained the expression of specific G1 phase cyclin-dependent kinase inhibitors and concomitantly induced a dynamic expression profile of key anti-apoptotic regulators. This study provides the first evidence of the underlying mechanism by which a member of the NeuroD-subfamily promotes an active anti-apoptotic program essential to the survival of neurons. Our results suggest that the survival program may be viewed as an integral component of the intrinsic programming of the differentiated state.
基本螺旋-环-螺旋转录因子Nex1/Math-2属于NeuroD亚家族,该亚家族在神经元分化和维持分化状态过程中发挥关键作用。此前,我们证明Nex1是神经生长因子(NGF)通路的关键调控成分。本研究进一步支持了这一假说,结果表明Nex1具有与NGF相似的促存活特性,因为过表达Nex1的PC12细胞在无营养因子的情况下仍能存活。我们剖析了Nex1在血清去除后赋予神经保护作用的分子机制,发现Nex1的组成型表达维持了特定G1期细胞周期蛋白依赖性激酶抑制剂的表达,并同时诱导了关键抗凋亡调节因子的动态表达谱。本研究首次提供了证据,证明NeuroD亚家族的一个成员促进对神经元存活至关重要的主动抗凋亡程序的潜在机制。我们的结果表明,存活程序可被视为分化状态固有编程的一个组成部分。