Melanocortin-3 receptor activates MAP kinase via PI3 kinase

Abstract

HEK 293 cells stably expressing human melanocortin-3 receptor (MC3R) were exposed to melanocortin receptor agonist, NDP-MSH (10 − 10–10 − 6 M). ERK1/2 was phosphorylated in a dose-dependent manner with an EC 50 of 3.3 ± 1.5 × 10 − 9 M, similar to the IC 50 of NDP-MSH binding to the MC3R. ERK1/2 phosphorylation was blocked by the melanocortin receptor antagonists SHU9119. NDP-MSH-induced ERK1/2 phosphorylation was sensitive to pertussis toxin and the PI3K inhibitor, wortmannin. Rp-cAMPS, BAPTA-AM and Myr-PKC did not inhibit the NDP-MSH-induced ERK1/2 phosphorylation. NDP-MSH stimulated cellular proliferation in a dose-dependent manner with a similar EC 50 to ERK1/2 phosphorylation, 2.1 ± 0.6 × 10 − 9 M. Cellular proliferation was blocked by AGRP (86–132) and by the MEK inhibitor, PD98059. The NDP-MSH did not inhibit serum deprivation-induced apoptosis. MC3R activation induces ERK1/2 phosphorylation via PI3K and this pathway is involved in cellular proliferation in HEK cells expressing MC3R.