TY - JOUR
T1 - Activation of microtubule dynamics increases neuronal growth via the Nerve Growth Factor (NGF)- and Gαs-mediated signaling pathways
AU - Sarma, Tulika
AU - Koutsouris, Athanasia
AU - Yu, Jiang Zhu
AU - Krbanjevic, Aleksandar
AU - Hope, Thomas J.
AU - Rasenick, Mark M.
N1 - Publisher Copyright:
© 2015, American Society for Biochemistry and Molecular Biology Inc. All rights reserved.
PY - 2015/4/17
Y1 - 2015/4/17
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=84927728947&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84927728947&partnerID=8YFLogxK
U2 - 10.1074/jbc.M114.630632
DO - 10.1074/jbc.M114.630632
M3 - Article
C2 - 25691569
AN - SCOPUS:84927728947
SN - 0021-9258
VL - 290
SP - 10045
EP - 10056
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 16
ER -