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PMID: 17038640 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Cyclic AMP imaging in adult cardiac myocytes reveals far-reaching beta1-adrenergic but locally confined beta2-adrenergic receptor-mediated signaling.

Circulation research ·Vol. 99 ·No. 10 ·2006-11-10 ·Pages 1084-91

Nikolaev VO, Bünemann M, Schmitteckert E, Lohse MJ, Engelhardt S

Abstract

Beta(1)- and beta(2)-adrenergic receptors (betaARs) are known to differentially regulate cardiomyocyte contraction and growth. We tested the hypothesis that these differences are attributable to spatial compartmentation of the second messenger cAMP. Using a fluorescent resonance energy transfer (FRET)-based approach, we directly monitored the spatial and temporal distribution of cAMP in adult cardiomyocytes. We developed a new cAMP-FRET sensor (termed HCN2-camps) based on a single cAMP binding domain of the hyperpolarization activated cyclic nucleotide-gated potassium channel 2 (HCN2). Its cytosolic distribution, high dynamic range, and sensitivity make HCN2-camps particularly well suited to monitor subcellular localization of cardiomyocyte cAMP. We generated HCN2-camps transgenic mice and performed single-cell FRET imaging on freshly isolated cardiomyocytes. Whole-cell superfusion with isoproterenol showed a moderate elevation of cAMP. Application of various phosphodiesterase (PDE) inhibitors revealed stringent control of cAMP through PDE4>PDE2>PDE3. The beta(1)AR-mediated cAMP signals were entirely dependent on PDE4 activity, whereas beta(2)AR-mediated cAMP was under control of multiple PDE isoforms. beta(1)AR subtype-specific stimulation yielded approximately 2-fold greater cAMP responses compared with selective beta(2)-subtype stimulation, even on treatment with the nonselective PDE inhibitor 3-isobutyl-1-methylxanthine (IBMX) (DeltaFRET, 17.3+/-1.3% [beta(1)AR] versus 8.8+/-0.4% [beta(2)AR]). Treatment with pertussis toxin to inactivate G(i) did not affect cAMP production. Localized beta(1)AR stimulation generated a cAMP gradient propagating throughout the cell, whereas local beta(2)AR stimulation did not elicit marked cAMP diffusion. Our data reveal that in adult cardiac myocytes, beta(1)ARs induce far-reaching cAMP signals, whereas beta(2)AR-induced cAMP remains locally confined.

MeSH Terms
Adrenergic beta-Agonists/pharmacology Animals Biosensing Techniques/methods Cyclic AMP/genetics,metabolism Fluorescence Resonance Energy Transfer/methods Humans Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels Ion Channels/biosynthesis,genetics,metabolism Isoenzymes/metabolism Mice Mice, Transgenic Models, Molecular Myocytes, Cardiac/cytology,metabolism Phosphoric Diester Hydrolases/metabolism Potassium Channels Protein Structure, Tertiary Receptors, Adrenergic, beta-1/metabolism Receptors, Adrenergic, beta-2/metabolism Signal Transduction
Chemicals
Adrenergic beta-Agonists HCN2 protein, human Hcn2 protein, mouse Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels Ion Channels Isoenzymes Potassium Channels Receptors, Adrenergic, beta-1 Receptors, Adrenergic, beta-2 Cyclic AMP Phosphoric Diester Hydrolases
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Nikolaev Viacheslav O
Institute of Pharmacology and Toxicology, University of Wuerzburg, Germany.
Bünemann Moritz
Schmitteckert Eva
Lohse Martin J
Engelhardt Stefan
Article Info
Journal
Circulation research
Abbr.
Circ Res
ISSN
1524-4571
Published
2006-11-10
Epub
2006-00-12
Pages
1084-91
Language
English
Region
United States
NLM ID
0047103
Subset
IM
Corrections
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