Phosphorylation of cardiac sodium channel at Ser571 anticipates manifestations of the aging myopathy

Author:

Pizzo Emanuele1ORCID,Cervantes Daniel O.1,Ketkar Harshada2,Ripa Valentina1,Nassal Drew M.34,Buck Benjamin5,Parambath Sreema P.2,Di Stefano Valeria1,Singh Kanwardeep1,Thompson Carl I.1,Mohler Peter J.356,Hund Thomas J.345,Jacobson Jason T.17,Jain Sudhir2ORCID,Rota Marcello1ORCID

Affiliation:

1. Department of Physiology, New York Medical College, Valhalla, New York, United States

2. Department of Pathology, Microbiology and Immunology, New York Medical College, Valhalla, New York, United States

3. The Frick Center for Heart Failure and Arrhythmia, Dorothy M. Davis Heart and Lung Research Institute, The Ohio State University Wexner Medical Center, Columbus, Ohio, United States

4. Department of Biomedical Engineering, College of Engineering, The Ohio State University, Columbus, Ohio, United States

5. Division of Cardiovascular Medicine, Department of Internal Medicine, The Ohio State University, Columbus, Ohio, United States

6. Department of Physiology and Cell Biology, The Ohio State University College of Medicine, Columbus, Ohio, United States

7. Department of Cardiology, Westchester Medical Center, Valhalla, New York, United States

Abstract

We have investigated the impact of the late Na current ( INa,L) on cardiac and myocyte function with aging by using genetically engineered animals with enhanced or stabilized INa,L, due to phosphomimetic or phosphoablated mutations of Nav1.5. Our findings support the notion that phosphorylation of Nav1.5 at Ser571 prolongs myocardial repolarization and impairs diastolic function, contributing to the manifestations of the aging myopathy.

Funder

University of Parma

American Heart Association

HHS | National Institutes of Health

New York Medical College

Publisher

American Physiological Society

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