Regulation of cAMP homeostasis by the efflux protein MRP4 in cardiac myocytes
Year: 2011
Type: article
Abstract: Recent studies indicate that members of the multidrug‐resistance protein ( MRP ) family belonging to ATP binding cassette type C ( ABCC ) membrane proteins extrude cyclic nucleotides from various cell types. This study aimed to determine whether MRP proteins regulate cardiac cAMP homeostasis. Here, we demonstrate that MRP4 is the predominant isoform present at the plasma membrane of cardiacmyocytes and that it mediates the efflux of cAMP in these cells. MRP4‐deficient mice displayed enhanced cardiac myocyte cAMP formation, contractility, and cardiac hypertrophy at 9 mo of age, an effect that was compensated transiently by increased phosphodiesterase expression at young age. These findings suggest that cAMP extrusion via MRP4 acts together with phosphodiesterases to control cAMP levels in cardiac myocytes.—Sassi, Y., Abi‐Gerges, A., Fauconnier, J., Mougenot, N., Reiken, S., Haghighi, K., Kranias, E. G., Marks, A. R., Lacampagne, A., Engelhardt, S., Hatem, S. N., Lompre, A.‐M., Hulot, J. S. Regulation of cAMP homeostasis by the efflux protein MRP4 in cardiac myocytes. FASEB J. 26, 1009‐1017 (2012). www.fasebj.org
Source: The FASEB Journal
DOI: 10.1096/fj.11-194027
Institutions: Inserm, Université Pierre-et-Marie-Curie, Technical University of Munich, Université de Montpellier, Physiologie et Médecine Expérimentale du Coeur et des Muscles, Columbia University Irving Medical Center, Columbia University, University of Cincinnati, Icahn School of Medicine at Mount Sinai
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: green
OpenAlex ID: W2111908003
