Journal
MOLECULAR PHARMACOLOGY
Volume 77, Issue 3, Pages 327-338Publisher
AMER SOC PHARMACOLOGY EXPERIMENTAL THERAPEUTICS
DOI: 10.1124/mol.109.061440
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Funding
- National Institutes of Health National Institute of Mental Health Psychoactive Drug Screening Program [R01-MH61887, U19-MH82441]
- Michael Hooker Chair for Therapeutics and Translational Proteomics
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The concept of functional selectivity has now thoroughly supplanted the previously entrenched notion of intrinsic efficacy by explaining how agonists and antagonists exhibit a range of efficacies for distinct receptor-mediated responses. It is noteworthy that functional selectivity accommodates significant changes in efficacy resulting from differential expression of G protein-coupled receptor modifying proteins (i.e., conditional efficacy)-a phenomenon with profound implications for drug discovery. We have uncovered a novel regulatory mechanism whereby p90 ribosomal S6 kinase 2 (RSK2) interacts with 5-hydroxytryptamine(2A) (5-HT2A) serotonin receptors and attenuates receptor signaling via direct receptor phosphorylation (Proc Natl Acad Sci U S A 103: 4717-4722, 2006; J Biol Chem 284: 5557-5573, 2009). This discovery, together with the mounting evidence for conditional efficacy, suggested to us that 5-HT2A agonist signaling might be disproportionately affected by alterations in RSK2 expression. To test this hypothesis, we evaluated a chemically diverse set of 5-HT2A agonists at three readouts of 5-HT2A receptor activation in both wild-type (WT) and RSK2 knockout (KO) mouse embryonic fibroblasts (MEFs). Here we report that 5-HT2A receptor agonist efficacies were significantly and variably augmented in RSK2 KO MEFs compared with WT MEFs. As a result, relative agonist efficacies were significantly altered, and even reversed, between WT and RSK2 KO MEFs for a single effector readout. This study provides the first evidence that deletion of a single kinase can elicit profound changes in patterns of agonist functional selectivity.
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