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Plasma Membrane Calcium Pump (PMCA4)-Neuronal Nitric-oxide Synthase Complex Regulates Cardiac Contractility through Modulation of a Compartmentalized Cyclic Nucleotide Microdomain
Faculty
Pharmacy
Year:
2011
Type of Publication:
Article
Pages:
41520-41529
Authors:
Mohamed, Tamer M. A, Abou-Leisa, Riham, Baudoin, Florence, Neyses, Ludwig, Cartwright, Elizabeth J, Oceandy, Delvac, Zi, Min, Prehar, Sukhpal, Alatwi, Nasser, Wang, Yanwen, Shaheen, Mohamed A, Schelcher, Celine, Hegab, Zeinab, Emerson, Michael, Mamas, Mamas, Di Benedetto, Giulietta, Zaccolo, Manuela, Lei, Ming
DOI:
10.1074/jbc.M111.290411
Journal:
JOURNAL OF BIOLOGICAL CHEMISTRY AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
Volume:
286
Research Area:
Biochemistry \& Molecular Biology
ISSN
ISI:000298057500038
Keywords :
Plasma Membrane Calcium Pump (PMCA4)-Neuronal Nitric-oxide
Abstract:
Identification of the signaling pathways that regulate cyclic nucleotide microdomains is essential to our understanding of cardiac physiology and pathophysiology. Although there is growing evidence that the plasma membrane Ca2+/calmodulinde-pendent ATPase 4 (PMCA4) is a regulator of neuronal nitricoxide synthase, the physiological consequence of this regulation is unclear. We therefore tested the hypothesis that PMCA4 has a key structural role in tethering neuronal nitric-oxide synthase to a highly compartmentalized domain in the cardiac cell membrane. This structural role has functional consequences on cAMP and cGMP signaling in a PMCA4-governed microdomain, which ultimately regulates cardiac contractility. In vivo contractility and calcium amplitude were increased in PMCA4 knock-out animals (PMCA4(-/-)) with no change in diastolic relaxation or the rate of calcium decay, showing that PMCA4 has a function distinct from beat-to-beat calcium transport. Surprisingly, in PMCA4(-/-), over 36\% of membrane-associated neuronal nitric-oxide synthase (nNOS) protein and activity was delocalized to the cytosol with no change in total nNOS protein, resulting in a significant decrease in microdomain cGMP, which in turn led to a significant elevation in local cAMP levels through a decrease in PDE2 activity (measured by FRET-based sensors). This resulted in increased L-type calcium channel activity and ryanodine receptor phosphorylation and hence increased contractility. In the heart, in addition to subsarcolemmal calcium transport, PMCA4 acts as a structural molecule that maintains the spatial and functional integrity of the nNOS signaling complex in a defined microdomain. This has profound consequences for the regulation of local cyclic nucleotide and hence cardiac (beta-adrenergic signaling.
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