MRAP2 inhibits ?-arrestin recruitment to the ghrelin receptor by preventing GHSR1a phosphorylation

The melanocortin receptor accessory protein 2 (MRAP2) is essential for several physiological functions of the ghrelin receptor growth hormone secretagogue receptor 1a (GHSR1a), including increasing appetite and suppressing insulin secretion. In the absence of MRAP2, GHSR1a displays high constitutive activity and a weak G-protein-mediated response to ghrelin and readily recruits fl-arrestin. In the presence of MRAP2, however, G-protein-mediated signaling via GHSR1a is strongly dependent on ghrelin stimulation and the recruitment of fl-arrestin is significantly diminished. To better understand how MRAP2 modifies GHSR1a signaling, here we investigated the role of several phosphorylation sites within the C-terminal tail and third intracellular loop of GHSR1a, as well as the mechanism behind MRAP2-mediated inhibition of fl-arrestin recruitment. We show that Ser252 and Thr261 in the third intracellular loop of GHSR1a contribute to fl-arrestin recruitment, whereas the Cterminal region is not essential for fl-arrestin interaction. Additionally, we found that MRAP2 inhibits GHSR1a phosphorylation by blocking the interaction of GRK2 and PKC with the receptor. Taken together, these data suggest that MRAP2 alters GHSR1a signaling by directly impacting the phosphorylation state of the receptor and that the C-terminal tail of GHSR1a prevents rather than contribute to flarrestin recruitment.

Automated summary

The melanocortin receptor accessory protein 2 (MRAP2) plays a crucial role in modulating the signaling pathway of the ghrelin receptor growth hormone secretagogue receptor 1a (GHSR1a), affecting appetite and insulin secretion. By altering the phosphorylation state of GHSR1a and inhibiting the interaction of GRK2 and PKC with the receptor, MRAP2 modifies GHSR1a signaling and diminishes the recruitment of fl-arrestin.