Trends in Cardiovascular Medicine
Volume 15, Issue 1 , Pages 35-40, January 2005

Regulation of the Voltage-Gated Cardiac Sodium Channel Nav1.5 by Interacting Proteins

  • Hugues Abriel

      Affiliations

    • Corresponding Author InformationAddress correspondence to: H. Abriel, MD, PhD, SNF-Professor, University of Lausanne, Department of Pharmacology and Toxicology and Service of Cardiology, Bugnon, 27, 1005 Lausanne, Switzerland. Tel.: +41 21 6925364; fax: +41 21 6935355
  • ,
  • Robert S. Kass

Hugues Abriel is at the Department of Pharmacology and Toxicology, Service of Cardiology, University of Lausanne, Switzerland. Robert S. Kass is at the Department of Pharmacology, College of Physicians and Surgeons of Columbia University, New York, New York

Nav1.5, the major cardiac voltage-gated Na+ channel, plays a central role in the generation of the cardiac action potential and in the propagation of electrical impulses in the heart. Its importance for normal heart function has been recently exemplified by reports of numerous mutations found in the gene SCN5A—which encodes Nav1.5—in patients with various pathologic cardiac phenotypes, indicating that even subtle alterations of Nav1.5 cell biology and function may underlie human diseases. Similar to other ion channels, Nav1.5 is most likely part of dynamic multiprotein complexes located in the different cellular compartments. This review focuses on five intracellular proteins that have been recently reported to directly bind to and contribute to the regulation of Nav1.5: ankyrin proteins, fibroblast growth factor homologous factor 1B, calmodulin, Nedd4-like ubiquitin-protein ligases, and syntrophin proteins.

 

PII: S1050-1738(05)00002-2

doi:10.1016/j.tcm.2005.01.001

Trends in Cardiovascular Medicine
Volume 15, Issue 1 , Pages 35-40, January 2005