COMPARATIVE EFFECTS OF CTP-GAMMA-S AND INSULIN ON THE ACTIVATION OF RHO, PHOSPHATIDYLINOSITOL 3-KINASE, AND PROTEIN-KINASE-N IN RAT ADIPOCYTES - RELATIONSHIP TO GLUCOSE-TRANSPORT

Electroporation of rat adipocytes with guanosine 5'-3-O-(thio)triphosp hate (GTP gamma S) elicited sizable insulinlike increases in glucose t ransport and GLUT4 translocation. Like insulin, GTP gamma S activated membrane phosphatidylinositol (PI) 3-kinase in rat adipocytes, but, un like insulin, this activation was blocked by Clostridium botulinum C3 transferase, suggesting a requirement for the small G-protein, RhoA. A lso suggesting that Rho may operate upstream of PI 3-kinase during GTP gamma S action, the stable overexpression of Rho in 3T3/L1 adipocytes provoked increases in membrane PI 3-kinase activity. As with insulin treatment, GTP gamma S stimulation of glucose transport in rat adipocy tes was blocked by C3 transferase, wortmannin, LY294002, and RO 31-822 0; accordingly, the activation of glucose transport by GTP gamma S, as well as insulin, appeared to require Rho, PI S-kinase, and another do wnstream kinase, e.g. protein kinase C-zeta (PKC-zeta) and/or protein kinase N (PKN). Whereas insulin activated both PKN and PKC-zeta, GTP g amma S activated PKN but not PKC-zeta. In transfection studies in 3T3/ L1 cells, stable expression of wild-type Rho and PKN activated glucose transport, and dominant-negative forms of Rho and PKN inhibited insul in stimulated glucose transport. In transfection studies in rat adipoc ytes, transient expression of wild-type and constitutive Rho and wildt ype PI(N provoked increases in the translocation of hemagglutinin (HA) -tagged GLUT4 to the plasma membrane; in contrast, transient expressio n of dominant-negative forms of Rho and PKN inhibited the effects of b oth insulin and GTP gamma S on HA-GLUT4 translocation. Our findings su ggest that (a) GTP gamma S and insulin activate Rho, PI S-kinase, and PKN, albeit by different mechanisms; (b) each of these signaling subst ances appears to be required for, and may contribute to, increases in glucose transport; and (c) PKC-zeta may contribute to increases in glu cose transport during insulin, but not GTP gamma S, action.