Article (Périodiques scientifiques)
Plasma membrane calcium ATPase and its relationship to nitric oxide signaling in the heart.
Cartwright, Elizabeth J.; Oceandy, Delvac; NEYSES, Ludwig
2007In Annals of the New York Academy of Sciences, 1099, p. 247-53
Peer reviewed
 

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Plasma Membrane Calcium ATPase and Its Relationship to Nitric Oxide Signaling in the Heart.pdf
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Mots-clés :
Calcium-Transporting ATPases/metabolism; Cell Membrane/enzymology; Myocardium/enzymology/metabolism; Nitric Oxide/metabolism; Nitric Oxide Synthase Type I/metabolism; Signal Transduction
Résumé :
[en] The plasma membrane calcium/calmodulin-dependent ATPase (PMCA) is a ubiquitously expressed calcium-extruding enzymatic pump. In the majority of cells the main function of PMCA is as the only system to extrude calcium from the cytosol, however, in the excitable cells of the heart it has only a minor role in the bulk removal of calcium compared to the sodium-calcium exchanger. There is increasing evidence to suggest that PMCA has an additional role as a potential modulator of a number of signal transduction pathways. Of key interest in the heart is the functional interaction between the calcium/calmodulin-dependent enzyme neuronal nitric oxide synthase (nNOS) and isoform 4 of PMCA. Nitric oxide production from nNOS is known to be important in the regulation of excitation-contraction (EC) coupling and subsequently contractility. This article will focus on recent evidence suggesting that PMCA4 has a regulatory role in the nitric oxide signaling pathway in the heart.
Disciplines :
Systèmes cardiovasculaire & respiratoire
Auteur, co-auteur :
Cartwright, Elizabeth J.
Oceandy, Delvac
NEYSES, Ludwig ;  University of Luxembourg > Central Administration ; University of Luxembourg > Research Office
Langue du document :
Anglais
Titre :
Plasma membrane calcium ATPase and its relationship to nitric oxide signaling in the heart.
Date de publication/diffusion :
2007
Titre du périodique :
Annals of the New York Academy of Sciences
ISSN :
0077-8923
Volume/Tome :
1099
Pagination :
247-53
Peer reviewed :
Peer reviewed
Disponible sur ORBilu :
depuis le 16 octobre 2014

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