Published online before print November 17, 2005, doi: 10.1161/01.RES.0000196568.11624.ae
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© 2005 American Heart Association, Inc.
Integrative Physiology |
Nuclear Targeting of Akt Enhances Ventricular Function and Myocyte Contractility
From the Cardiovascular Research Institute (M.R., A.B., K.U., M.E.P.-I., T.J.K., G.F., E.H.S., E.M., A.L., P.A.), Department of Medicine, New York Medical College, Valhalla; Cardiovascular Research Center (H.K., S.R.H.), Temple University, Philadelphia, Pa; and San Diego State University Heart Institute (M.A.S.), Calif; and Tardini-Vitali-Mazza-Olivetti Stem Cell Center (E.M.), Parma, Italy.
Correspondence to Piero Anversa, MD, Cardiovascular Research Institute, Vosburgh Pavilion, Rm 302, New York Medical College, Valhalla, NY 10595. E-mail piero_anversa{at}nymc.edu
Cytoplasmic overexpression of Akt in the heart results in a myopathy characterized by organ and myocyte hypertrophy. Conversely, nuclear-targeted Akt does not lead to cardiac hypertrophy, but the cellular basis of this distinct heart phenotype remains to be determined. Similarly, whether nuclear-targeted Akt affects ventricular performance and mechanics, calcium metabolism, and electrical properties of myocytes is unknown. Moreover, whether the expression and state of phosphorylation of regulatory proteins implicated in calcium cycling and myocyte contractility are altered in nuclear-targeted Akt has not been established. We report that nuclear overexpression of Akt does not modify cardiac size and shape but results in an increased number of cardiomyocytes, which are smaller in volume. Additionally, the heart possesses enhanced systolic and diastolic function, which is paralleled by increased myocyte performance. Myocyte shortening and velocity of shortening and relengthening are increased in transgenic mice and are coupled with a more efficient reuptake of calcium by the sarcoplasmic reticulum (SR). This process increases calcium loading of the SR during relengthening. The enhanced SR function appears to be mediated by an increase in SR Ca2+-ATPase2a activity sustained by a higher degree of phosphorylation of phospholamban. This posttranslational modification was associated with an increase in phospho–protein kinase A and a decrease in protein phosphatase-1. Together, these observations provide a plausible biochemical mechanism for the potentiation of myocyte and ventricular function in Akt transgenic mice. Therefore, nuclear-targeted Akt in myocytes may have important implications for the diseased heart.
Key Words: Akt • myocyte mechanics • myocyte size and number
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