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PMID: 8663433 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, P.H.S.

G protein-coupled receptor kinase specificity for phosphorylation and desensitization of alpha2-adrenergic receptor subtypes.

The Journal of biological chemistry ·Vol. 271 ·No. 30 ·1996-07-26 ·Pages 18082-7

Jewell-Motz EA, Liggett SB

Abstract

The alpha2-adrenergic receptor (alpha2AR) subtype alpha2C10 undergoes rapid agonist-promoted desensitization which is due to phosphorylation of the receptor. One kinase that has been shown to phosphorylate alpha2C10 in an agonist-dependent manner is the betaAR kinase (betaARK), a member of the family of G protein-coupled receptor kinases (GRKs). In contrast, the alpha2C4 subtype has not been observed to undergo agonist-promoted desensitization or phosphorylation by betaARK. However, the substrate specificities of the GRKs for phosphorylating alpha2AR subtypes are not known. We considered that differential capacities of various GRKs to phosphorylate alpha2C10 and alpha2C4 might be a key factor in dictating in a given cell the presence or extent of agonist-promoted desensitization of these receptors. COS-7 cells were co-transfected with alpha2C10 or alpha2C4 without or with the following GRKs: betaARK, betaARK2, GRK5, or GRK6. Intact cell phosphorylation studies were carried out by labeling cells with 32Pi, exposing some to agonist, and purifying the alpha2AR by immunoprecipitation and SDS-polyacrylamide gel electrophoresis. BetaARK and betaARK2 were both found to phosphorylate alpha2C10 to equal extents (>2-fold over that of the endogenous kinases). On the other hand, GRK5 and GRK6 did not phosphorylate alpha2C10. In contrast to the findings with alpha2C10, alpha2C4 was not phosphorylated by any of these kinases. Functional studies carried out in transfected HEK293 cells expressing alpha2C10 or alpha2C4 and selected GRKs were consistent with these phosphorylation results. With the marked expression of these receptors, no agonist-promoted desensitization was observed in the absence of GRK co-expression. However, desensitization was imparted to alpha2C10 by co-expression of betaARK but not GRK6, while alpha2C4 failed to desensitize with co-expression of betaARK. These results indicate that short term agonist-promoted desensitization of alpha2ARs by phosphorylation is dependent on both the receptor subtype and the expressed GRK isoform.

MeSH Terms
Adrenergic beta-Agonists/pharmacology Animals Cattle Cyclic AMP-Dependent Protein Kinases/genetics,metabolism GTP-Binding Proteins/metabolism Humans Isoenzymes/metabolism Phosphorylation Receptor Protein-Tyrosine Kinases/genetics,metabolism Receptors, Adrenergic, alpha-2/metabolism Recombinant Proteins/metabolism Signal Transduction beta-Adrenergic Receptor Kinases
Chemicals
Adrenergic beta-Agonists Isoenzymes Receptors, Adrenergic, alpha-2 Recombinant Proteins Receptor Protein-Tyrosine Kinases Cyclic AMP-Dependent Protein Kinases beta-Adrenergic Receptor Kinases GTP-Binding Proteins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Jewell-Motz E A
Department of Medicine, University of Cincinnati, Cincinnati, Ohio 45267-0564, USA.
Liggett S B
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1996-07-26
Pages
18082-7
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NHLBI NIH HHS · HL07382 · United States
NHLBI NIH HHS · HL41496 · United States
NHLBI NIH HHS · HL53436 · United States
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