Threonine 180 is required for G-protein-coupled receptor kinase 3- and beta-arrestin 2-mediated desensitization of the mu-opioid receptor in Xenopus oocytes.

Celver JP, Lowe J, Kovoor A, Gurevich VV, Chavkin C
J Biol Chem. 2001 276 (7): 4894-900

PMID: 11060299 · DOI:10.1074/jbc.M007437200

To determine the sites in the mu-opioid receptor (MOR) critical for agonist-dependent desensitization, we constructed and coexpressed MORs lacking potential phosphorylation sites along with G-protein activated inwardly rectifying potassium channels composed of K(ir)3.1 and K(ir)3.4 subunits in Xenopus oocytes. Activation of MOR by the stable enkephalin analogue, [d-Ala(2),MePhe(4),Glyol(5)]enkephalin, led to homologous MOR desensitization in oocytes coexpressing both G-protein-coupled receptor kinase 3 (GRK3) and beta-arrestin 2 (arr3). Coexpression with either GRK3 or arr3 individually did not significantly enhance desensitization of responses evoked by wild type MOR activation. Mutation of serine or threonine residues to alanines in the putative third cytoplasmic loop and truncation of the C-terminal tail did not block GRK/arr3-mediated desensitization of MOR. Instead, alanine substitution of a single threonine in the second cytoplasmic loop to produce MOR(T180A) was sufficient to block homologous desensitization. The insensitivity of MOR(T180A) might have resulted either from a block of arrestin activation or arrestin binding to MOR. To distinguish between these alternatives, we expressed a dominant positive arrestin, arr2(R169E), that desensitizes G protein-coupled receptors in an agonist-dependent but phosphorylation-independent manner. arr2(R169E) produced robust desensitization of MOR and MOR(T180A) in the absence of GRK3 coexpression. These results demonstrate that the T180A mutation probably blocks GRK3- and arr3-mediated desensitization of MOR by preventing a critical agonist-dependent receptor phosphorylation and suggest a novel GRK3 site of regulation not yet described for other G-protein-coupled receptors.

MeSH Terms (17)

Animals Arrestins beta-Arrestins Dose-Response Relationship, Drug Down-Regulation Enkephalin, Ala(2)-MePhe(4)-Gly(5)- G-Protein-Coupled Receptor Kinase 3 G Protein-Coupled Inwardly-Rectifying Potassium Channels Mutagenesis, Site-Directed Oocytes Phosphothreonine Potassium Channels Potassium Channels, Inwardly Rectifying Protein-Serine-Threonine Kinases Receptors, Opioid, mu Transfection Xenopus

Connections (1)

This publication is referenced by other Labnodes entities: