Department of Pathophysiology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, People's Republic of China.
J Neurosci. 2010 Mar 10;30(10):3839-48. doi: 10.1523/JNEUROSCI.5174-09.2010.
Protein phosphatase 2A (PP2A) is indispensable in development, and deficits of PP2A and deterioration of neuronal axons have been observed in several neurodegenerative disorders, but the direct link between PP2A and the neuronal axon development is still missing. Here, we show that PP2A is essential for axon development in transfected rat brain and the dissociated hippocampal neurons. Upregulation of PP2A catalytic subunit (PP2Ac) not only promotes formation and elongation of the functional axons but also rescues axon retardation induced by PP2A inhibition. PP2A can dephosphorylate collapsin response mediator protein-2 (CRMP2) that implements the axon polarization, whereas constitutive expression of phosphomimic-CRMP2 abrogates the effect of PP2A upregulation. We also demonstrate that PP2Ac is enriched in the distal axon of the hippocampal neurons. Our results reveal a mechanistic link between PP2A and axonogenesis/axonopathy, suggesting that upregulation of PP2A may be a promising therapeutic for some neurodegenerative disorders.
蛋白磷酸酶 2A(PP2A)在发育过程中不可或缺,并且在几种神经退行性疾病中已经观察到 PP2A 的缺陷和神经元轴突的恶化,但 PP2A 与神经元轴突发育之间的直接联系仍然缺失。在这里,我们表明 PP2A 对于转染大鼠脑和分离的海马神经元中的轴突发育是必不可少的。PP2A 催化亚基(PP2Ac)的上调不仅促进了功能性轴突的形成和伸长,而且还挽救了由 PP2A 抑制引起的轴突迟缓。PP2A 可以去磷酸化 collapsin 反应介质蛋白-2(CRMP2),该蛋白实施轴突极化,而组成型表达磷酸模拟-CRMP2 则消除了 PP2A 上调的作用。我们还证明 PP2Ac 富含在海马神经元的远端轴突中。我们的结果揭示了 PP2A 与轴发生/轴突病之间的机制联系,表明上调 PP2A 可能是治疗某些神经退行性疾病的有前途的方法。