Regulation of the cardiac Na+ channel NaV1.5 by post-translational modifications

• Published in: Journal of molecular and cellular cardiology Vol. 82; pp. 36 - 47
• Main Authors: Marionneau, Céline, Abriel, Hugues
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.05.2015; Elsevier
• Series: Equipe 1
• Subjects: Acetylation; Animals; Arrhythmias; Cardiac NaV1.5 channels; Gene Expression Regulation; Glycosylation; Humans; Life Sciences; Mass Spectrometry; Methylation; Native proteomics; NAV1.5 Voltage-Gated Sodium Channel - genetics; NAV1.5 Voltage-Gated Sodium Channel - metabolism; Oxidation-Reduction; Phosphorylation; Post-translational modifications; Protein Processing, Post-Translational; Proteomics - methods; Ubiquitination; Ac; BrS; pS; PKB/Akt; pT; MS; LQTS; PKA; NaV α subunit; PTM; Redox; PKC; pY; Cardiac NaV1.5 channels; INaL; CaMKII; Post-translational modifications; Native proteomics; PI3K; SGK; Me; AMPK; INa; Arrhythmias; Cardiac Na(V)1.5 channels; Cardiac Na V 15 channels
• ISSN: 0022-2828; 1095-8584; 1095-8584
• DOI: 10.1016/j.yjmcc.2015.02.013

The cardiac voltage-gated Na+ channel, NaV1.5, is responsible for the upstroke of the action potential in cardiomyocytes and for efficient propagation of the electrical impulse in the myocardium. Even subtle alterations of NaV1.5 function, as caused by mutations in its gene SCN5A, may lead to many different arrhythmic phenotypes in carrier patients. In addition, acquired malfunctions of NaV1.5 that are secondary to cardiac disorders such as heart failure and cardiomyopathies, may also play significant roles in arrhythmogenesis. While it is clear that the regulation of NaV1.5 protein expression and function tightly depends on genetic mechanisms, recent studies have demonstrated that NaV1.5 is the target of various post-translational modifications that are pivotal not only in physiological conditions, but also in disease. In this review, we examine the recent literature demonstrating glycosylation, phosphorylation by Protein Kinases A and C, Ca2+/Calmodulin-dependent protein Kinase II, Phosphatidylinositol 3-Kinase, Serum- and Glucocorticoid-inducible Kinases, Fyn and Adenosine Monophosphate-activated Protein Kinase, methylation, acetylation, redox modifications, and ubiquitylation of NaV1.5. Modern and sensitive mass spectrometry approaches, applied directly to channel proteins that were purified from native cardiac tissues, have enabled the determination of the precise location of post-translational modification sites, thus providing essential information for understanding the mechanistic details of these regulations. The current challenge is first, to understand the roles of these modifications on the expression and the function of NaV1.5, and second, to further identify other chemical modifications. It is postulated that the diversity of phenotypes observed with NaV1.5-dependent disorders may partially arise from the complex post-translational modifications of channel protein components. •The cardiac NaV1.5 channel is subject to PTMs whose roles are partially understood.•The majority of NaV1.5 PTM sites are located in the first loop of the channel.•The use of native channel proteomics is of high discovery and gain.•NaV1.5 PTMs contribute to cardiac disease, which may have therapeutic applications.