Insulin stimulates phosphatidylinositol 3-phosphate production via the activation of Rab5

IJ Lodhi, D Bridges, SH Chiang, Y Zhang… - Molecular biology of …, 2008 - Am Soc Cell Biol
IJ Lodhi, D Bridges, SH Chiang, Y Zhang, A Cheng, LM Geletka, LS Weisman, AR Saltiel
Molecular biology of the cell, 2008Am Soc Cell Biol
Phosphatidylinositol 3-phosphate (PI (3) P) plays an important role in insulin-stimulated
glucose uptake. Insulin promotes the production of PI (3) P at the plasma membrane by a
process dependent on TC10 activation. Here, we report that insulin-stimulated PI (3) P
production requires the activation of Rab5, a small GTPase that plays a critical role in
phosphoinositide synthesis and turnover. This activation occurs at the plasma membrane
and is downstream of TC10. TC10 stimulates Rab5 activity via the recruitment of GAPEX-5, a …
Phosphatidylinositol 3-phosphate (PI(3)P) plays an important role in insulin-stimulated glucose uptake. Insulin promotes the production of PI(3)P at the plasma membrane by a process dependent on TC10 activation. Here, we report that insulin-stimulated PI(3)P production requires the activation of Rab5, a small GTPase that plays a critical role in phosphoinositide synthesis and turnover. This activation occurs at the plasma membrane and is downstream of TC10. TC10 stimulates Rab5 activity via the recruitment of GAPEX-5, a VPS9 domain–containing guanyl nucleotide exchange factor that forms a complex with TC10. Although overexpression of plasma membrane-localized GAPEX-5 or constitutively active Rab5 promotes PI(3)P formation, knockdown of GAPEX-5 or overexpression of a dominant negative Rab5 mutant blocks the effects of insulin or TC10 on this process. Concomitant with its effect on PI(3)P levels, the knockdown of GAPEX-5 blocks insulin-stimulated Glut4 translocation and glucose uptake. Together, these studies suggest that the TC10/GAPEX-5/Rab5 axis mediates insulin-stimulated production of PI(3)P, which regulates trafficking of Glut4 vesicles.
Am Soc Cell Biol