Research ArticlePharmacology

Agonist-selective NOP receptor phosphorylation correlates in vitro and in vivo and reveals differential post-activation signaling by chemically diverse agonists

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Sci. Signal.  26 Mar 2019:
Vol. 12, Issue 574, eaau8072
DOI: 10.1126/scisignal.aau8072

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Delineating NOP agonists

The nociceptin/orphanin FQ peptide (NOP) receptor is the least well-characterized member of the opioid receptor family. Mann et al. developed phosphosite-specific antibodies for the NOP receptor and then analyzed in cultured cells and in mice the physical and temporal patterns of its activation, which differed in response to various agonists. Because NOP receptors are involved in various physiological processes—from learning and food intake to cardiovascular function and pain perception—these antibody tools and initial insights into agonist-specific NOP receptor activity should have broad biological and clinical implications.

Abstract

Agonists of the nociceptin/orphanin FQ opioid peptide (NOP) receptor, a member of the opioid receptor family, are under active investigation as novel analgesics, but their modes of signaling are less well characterized than those of other members of the opioid receptor family. Therefore, we investigated whether different NOP receptor ligands showed differential signaling or functional selectivity at the NOP receptor. Using newly developed phosphosite-specific antibodies to the NOP receptor, we found that agonist-induced NOP receptor phosphorylation occurred primarily at four carboxyl-terminal serine (Ser) and threonine (Thr) residues, namely, Ser346, Ser351, Thr362, and Ser363, and proceeded with a temporal hierarchy, with Ser346 as the first site of phosphorylation. G protein–coupled receptor kinases 2 and 3 (GRK2/3) cooperated during agonist-induced phosphorylation, which, in turn, facilitated NOP receptor desensitization and internalization. A comparison of structurally distinct NOP receptor agonists revealed dissociation in functional efficacies between G protein–dependent signaling and receptor phosphorylation. Furthermore, in NOP-eGFP and NOP-eYFP mice, NOP receptor agonists induced multisite phosphorylation and internalization in a dose-dependent and agonist-selective manner that could be blocked by specific antagonists. Our study provides new tools to study ligand-activated NOP receptor signaling in vitro and in vivo. Differential agonist-selective NOP receptor phosphorylation by chemically diverse NOP receptor agonists suggests that differential signaling by NOP receptor agonists may play a role in NOP receptor ligand pharmacology.

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