Stimulation of protein kinase C modulates insulin-like growth factor-1-induced Akt activation in PC12 cells

Activation of protein kinase C (PKC) plays an important role in the negativ e regulation of receptor signaling, but its effect on insulin-like growth f actor-1 (IGF-1) receptor signaling remains unclear. In this study, we chara cterized the intracellular pathways involved in IGF-1-induced activation of Akt and evaluated the effects of the PKC activator phorbol 12-myristate 13 -acetate (PMA) on the Akt activation by IGF-1. IGF-1 induced a time- and co ncentration-dependent activation of Akt. The effect of IGF-1 was blocked by the phosphatidylinositide 3-kinase (PI3K) inhibitors LY294002 (50 mu M) an d wortmannin (0.5 mu M), but not by the MEK inhibitor PD98059 (50 mu M) or the p70 S6 kinase pathway inhibitor rapamycin (50 nM), suggesting that the stimulation of Akt by IGF-1 is mediated by the PI3K pathway. Interestingly, cotreatment with PIMA (400 nM) attenuated IGF-1-induced activation of Akt. The attenuation was blocked completely by the PKC inhibitor GO6983 (0.5 mu M), but only partially by the MEK inhibitor PD98059 (50 mu M), indicating that MAPK-dependent and -independent pathways are involved. PMA induced the activation of PKC in PC12 cells, and this induction was blocked by GO6983. These data further support the role of PKC in the effect of PMA. Moreover, PKC delta is likely involved in the action of PMA on the basis of data obt ained using isoform-specific inhibitors such as rottlerin. PMA also decreas ed IGF-1-induced tyrosine phosphorylation of insulin receptor substrate-1 a nd its association with PI3K. Taken together, these results suggest, for th e first time, that stimulation of PKC modulates IGF-1-induced activation of Akt.