Caveolae-Independent Activation of Protein Kinase A in Rat Neonatal Myocytes

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  • Fukutomi Masashi
    Department of Pharmacology and Toxicology, Graduate School of Pharmaceutical Sciences, Kyushu University
  • Nishida Motohiro
    Department of Pharmacology and Toxicology, Graduate School of Pharmaceutical Sciences, Kyushu University
  • Maruyama Yoshiko
    Laboratory of Cellular Signaling, Graduate School of Pharmaceutical Sciences, University of Tokyo
  • Kobayashi Hiroyuki
    Department of Pharmacology and Toxicology, Graduate School of Pharmaceutical Sciences, Kyushu University
  • Kurose Hitoshi
    Department of Pharmacology and Toxicology, Graduate School of Pharmaceutical Sciences, Kyushu University

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Cardiomyocytes express both β1- and β2-adrenergic receptors, and these receptors play a differential role in chronotropic and inotropic effects of the heart. Caveolae are known as an important regulator of G-protein-coupled receptor signaling. In the present report, we examined whether caveolae have a role in β-adrenergic receptor-stimulated cAMP production and protein kinase A activation in neonatal myocytes. Isoproterenol-stimulated cAMP production was mediated by β1- and β2-subtypes, which depends on the receptor number of each subtype. However, protein kinase A activation was exclusively mediated by the β1-subtype. Disruption of caveolae by methyl-β-cyclodextrin treatment did not affect the relative contribution of subtypes to isoproterenol-stimulated cAMP production. β1-Subtype-mediated protein kinase A activation was also not affected by the disruption of caveolae. These results suggest that β1-adrenergic receptor-mediated protein kinase A activation is compartmentalized and independent of caveolae.<br>

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