AJP - Heart Calcium Transients and Cell-Sarcomere
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Am J Physiol Heart Circ Physiol 287: H1906-H1912, 2004. First published July 8, 2004; doi:10.1152/ajpheart.00356.2004
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TRANSLATIONAL PHYSIOLOGY

Adenylyl cyclase type VI corrects cardiac sarcoplasmic reticulum calcium uptake defects in cardiomyopathy

Tong Tang,1,3 Mei Hua Gao,1,3 David M. Roth,2,3 Tracy Guo,1,3 and H. Kirk Hammond1,3

1Departments of Medicine and 2Anesthesiology, University of California San Diego, San Diego 92093; and 3Veterans Affairs San Diego Healthcare System, San Diego, California 92161

Submitted 13 April 2004 ; accepted in final form 30 June 2004

Calcium malfunction plays a central role in heart failure. Here, we provide evidence that adenylyl cyclase type VI restores sarco(endo)plasmic reticulum 2a (SERCA2a) affinity for calcium and maximum velocity of cardiac calcium uptake by sarcoplasmic reticulum in murine dilated cardiomyopathy. Restoration of normal SERCA2a affinity for calcium is associated not only with decreased phospholamban protein expression but also with increased phospholamban phosphorylation by PKA activation. The ratio of phosphorylated ryanodine receptor 2 (RyR2) to RyR2 protein was increased, but the amount of phosphorylated RyR2 was unaffected. These data provide a possible mechanism by which adenylyl cyclase type VI (in contrast to other signaling elements associated with increased cAMP generation) has a salutary effect in the failing heart.

cAMP; {beta}-adrenergic receptor; myocardium; heart failure



Address for reprint requests and other correspondence: H. Kirk Hammond, 111A, VA San Diego Healthcare System, 3350 La Jolla Village Dr., San Diego, CA 92161 (E-mail: khammond{at}ucsd.edu)




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