Prevention of Cardiac Hypertrophy in Mice by Calcineurin Inhibition

Author:

Sussman Mark A.1,Lim Hae W.1,Gude Natalie1,Taigen Tyler1,Olson Eric N.1,Robbins Jeffrey1,Colbert Melissa C.1,Gualberto Antonio1,Wieczorek David F.1,Molkentin Jeffery D.1

Affiliation:

1. M. A. Sussman, H. W. Lim, N. Gude, T. Taigen, J. Robbins, M. C. Colbert, J. D. Molkentin, Division of Molecular Cardiovascular Biology, Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229, USA. E. N. Olson, Department of Molecular Biology and Oncology, University of Texas Southwestern Medical Center, Dallas, TX 75235, USA. A. Gualberto, Department of Physiology and Biophysics, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA. D. F. Wieczorek,...

Abstract

Hypertrophic cardiomyopathy (HCM) is an inherited form of heart disease that affects 1 in 500 individuals. Here it is shown that calcineurin, a calcium-regulated phosphatase, plays a critical role in the pathogenesis of HCM. Administration of the calcineurin inhibitors cyclosporin and FK506 prevented disease in mice that were genetically predisposed to develop HCM as a result of aberrant expression of tropomodulin, myosin light chain–2, or fetal β-tropomyosin in the heart. Cyclosporin had a similar effect in a rat model of pressure-overload hypertrophy. These results suggest that calcineurin inhibitors merit investigation as potential therapeutics for certain forms of human heart disease.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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