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微管动力学的激活通过神经生长因子(NGF)和Gαs介导的信号通路增加神经元生长。

Activation of microtubule dynamics increases neuronal growth via the nerve growth factor (NGF)- and Gαs-mediated signaling pathways.

作者信息

Sarma Tulika, Koutsouris Athanasia, Yu Jiang Zhu, Krbanjevic Aleksandar, Hope Thomas J, Rasenick Mark M

机构信息

From the Department of Physiology and Biophysics and.

From the Department of Physiology and Biophysics and Psychiatry, College of Medicine, University of Illinois at Chicago, Chicago, Illinois 60612.

出版信息

J Biol Chem. 2015 Apr 17;290(16):10045-56. doi: 10.1074/jbc.M114.630632. Epub 2015 Feb 17.

Abstract

Signals that activate the G protein Gαs and promote neuronal differentiation evoke Gαs internalization in rat pheochromocytoma (PC12) cells. These agents also significantly increase Gαs association with microtubules, resulting in an increase in microtubule dynamics because of the activation of tubulin GTPase by Gαs. To determine the function of Gαs/microtubule association in neuronal development, we used real-time trafficking of a GFP-Gαs fusion protein. GFP-Gαs concentrates at the distal end of the neurites in differentiated living PC12 cells as well as in cultured hippocampal neurons. Gαs translocates to specialized membrane compartments at tips of growing neurites. A dominant-negative Gα chimera that interferes with Gαs binding to tubulin and activation of tubulin GTPase attenuates neurite elongation and neurite number both in PC12 cells and primary hippocampal neurons. This effect is greatest on differentiation induced by activated Gαs. Together, these data suggest that activated Gαs translocates from the plasma membrane and, through interaction with tubulin/microtubules in the cytosol, is important for neurite formation, development, and outgrowth. Characterization of neuronal G protein dynamics and their contribution to microtubule dynamics is important for understanding the molecular mechanisms by which G protein-coupled receptor signaling orchestrates neuronal growth and differentiation.

摘要

激活G蛋白Gαs并促进神经元分化的信号可诱发大鼠嗜铬细胞瘤(PC12)细胞中的Gαs内化。这些因子还会显著增加Gαs与微管的结合,由于Gαs激活微管蛋白GTP酶,导致微管动力学增加。为了确定Gαs/微管结合在神经元发育中的功能,我们使用了GFP-Gαs融合蛋白的实时运输。GFP-Gαs集中在分化的活PC12细胞以及培养的海马神经元的神经突远端。Gαs转运到生长中神经突尖端的特殊膜区室。一种显性负性Gα嵌合体,它干扰Gαs与微管蛋白的结合以及微管蛋白GTP酶的激活,会减弱PC12细胞和原代海马神经元中的神经突伸长和神经突数量。这种效应在由激活的Gαs诱导的分化中最为明显。总之,这些数据表明,激活的Gαs从质膜转运,通过与胞质溶胶中的微管蛋白/微管相互作用,对神经突的形成、发育和生长很重要。表征神经元G蛋白动力学及其对微管动力学的贡献,对于理解G蛋白偶联受体信号传导协调神经元生长和分化的分子机制很重要。

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