Agonist-Regulated Internalization and Desensitization of the Human Nociceptin Receptor Expressed in CHO Cells

Title: Agonist-Regulated Internalization and Desensitization of the Human Nociceptin Receptor Expressed in CHO Cells

Volume: 8 Issue: 1

Author(s): S. Spampinato, M. Baiula and M. Calienni

Affiliation:

Keywords: Internalization, recycling, CHO-K1 cells, nociceptin, nociceptin receptor, desensitization, cAMP

Abstract: In this study we examined agonist-induced internalization of the cloned human nociceptin receptor (hNOP) expressed in CHOK1 cells. Internalization was proven by receptor binding assay on viable cells and confocal microscopy. The agonists nociceptin/orphanin FQ (NC), NC-NH2, NC(1-13)-NH2, [(pF)Phe4]NC-NH2 and RO 64-6198 promote a rapid, concentration-dependent internalization of the hNOP receptor. Under the same conditions, [Phe1,ψ (CH2NH)Gly2]NC(1-13)-NH2 and [Phe1, (CH2NH)Gly2,Arg14,Lys15]NC(1-13)-NH2 failed to induce significant, concentration-dependent NOP receptor endocytosis; even when present at high concentrations (up to 1 mM) they promoted only an approximately 25-30% internalization of hNOP receptors. We also investigated hNOP receptor desensitization upon agonist challenge: ligand efficacy to inhibit forskolin-stimulated cAMP production. After 1 h exposure to NC, NC-NH2, NC(1-13)- NH2, [(pF)Phe4]NC-NH2 and RO 64-6198 (5 μM) ≉20 to 30% of receptor desensitization was observed. Moreover, we found that the blockade of hNOP receptor recycling by monensin would cause a more prolonged and relevant desensitization of this receptor. The noninternalizing agonists [Phe1,ψ (CH2NH)Gly2]NC(1-13)-NH2 and [Phe1, (CH2NH)Gly2,Arg14,Lys15]NC(1-13)-NH2 (100 μM) resulted in a strong (67 and 74 %, respectively) receptor desensitization which was not influenced by monensin. Finally, CHO-hNOP cells exposed to the receptor-internalizing agonists for 24 h resulted in a significantly higher cAMP accumulation (defined supersensitization) compared with the non-internalizing agonists. In addition, blocking of receptor recycling by monensin led to a decrease of the cAMP accumulation only in cells exposed to internalizing agonists. These data show that prolonged receptor signaling mediated by receptor endocytosis and recycling/reactivation might reduce the development of tolerance but can enhance compensatory mechanisms that lead to supersensitivity of specific signaling pathways.

Cite this article as:

Spampinato S., Baiula M. and Calienni M., Agonist-Regulated Internalization and Desensitization of the Human Nociceptin Receptor Expressed in CHO Cells, Current Drug Targets 2007; 8 (1) . https://dx.doi.org/10.2174/138945007779315641