Functional protein expression of multiple sodium channel α- and β-subunit isoforms in neonatal cardiomyocytes

Susann G. Kaufmann, Ruth E. Westenbroek, Christoph Zechner, Alexander H. Maass, Sebastian Bischoff, Jenny Muck, Erhard Wischmeyer, Todd Scheuer, Sebastian K.G. Maier

Research output: Contribution to journalArticle

27 Citations (Scopus)

Abstract

Voltage-gated sodium channels are composed of pore-forming α- and auxiliary β-subunits and are responsible for the rapid depolarization of cardiac action potentials. Recent evidence indicates that neuronal tetrodotoxin (TTX) sensitive sodium channel α-subunits are expressed in the heart in addition to the predominant cardiac TTX-resistant Nav1.5 sodium channel α-subunit. These TTX-sensitive isoforms are preferentially localized in the transverse tubules of rodents. Since neonatal cardiomyocytes have yet to develop transverse tubules, we determined the complement of sodium channel subunits expressed in these cells. Neonatal rat ventricular cardiomyocytes were stained with antibodies specific for individual isoforms of sodium channel α- and β-subunits. α-actinin, a component of the z-line, was used as an intracellular marker of sarcomere boundaries. TTX-sensitive sodium channel α-subunit isoforms Nav1.1, Nav1.2, Nav1.3, Nav1.4 and Nav1.6 were detected in neonatal rat heart but at levels reduced compared to the predominant cardiac α-subunit isoform, Nav1.5. Each of the β-subunit isoforms (β1-β4) was also expressed in neonatal cardiac cells. In contrast to adult cardiomyocytes, the α-subunits are distributed in punctate clusters across the membrane surface of neonatal cardiomyocytes; no isoform-specific subcellular localization is observed. Voltage clamp recordings in the absence and presence of 20 nM TTX provided functional evidence for the presence of TTX-sensitive sodium current in neonatal ventricular myocardium which represents between 20 and 30% of the current, depending on membrane potential and experimental conditions. Thus, as in the adult heart, a range of sodium channel α-subunits are expressed in neonatal myocytes in addition to the predominant TTX-resistant Nav1.5 α-subunit and they contribute to the total sodium current.

Original languageEnglish (US)
Pages (from-to)261-269
Number of pages9
JournalJournal of Molecular and Cellular Cardiology
Volume48
Issue number1
DOIs
StatePublished - Jan 1 2010

Fingerprint

Sodium Channels
Tetrodotoxin
Cardiac Myocytes
Protein Isoforms
Proteins
Sodium
Voltage-Gated Sodium Channels
Actinin
Sarcomeres
Membrane Potentials
Muscle Cells
Action Potentials
Rodentia
Myocardium
Membranes
Antibodies

Keywords

  • Immunocytochemistry
  • Ion channels
  • Myocytes
  • Na-channel
  • Tetrodotoxin

ASJC Scopus subject areas

  • Molecular Biology
  • Cardiology and Cardiovascular Medicine

Cite this

Functional protein expression of multiple sodium channel α- and β-subunit isoforms in neonatal cardiomyocytes. / Kaufmann, Susann G.; Westenbroek, Ruth E.; Zechner, Christoph; Maass, Alexander H.; Bischoff, Sebastian; Muck, Jenny; Wischmeyer, Erhard; Scheuer, Todd; Maier, Sebastian K.G.

In: Journal of Molecular and Cellular Cardiology, Vol. 48, No. 1, 01.01.2010, p. 261-269.

Research output: Contribution to journalArticle

Kaufmann, SG, Westenbroek, RE, Zechner, C, Maass, AH, Bischoff, S, Muck, J, Wischmeyer, E, Scheuer, T & Maier, SKG 2010, 'Functional protein expression of multiple sodium channel α- and β-subunit isoforms in neonatal cardiomyocytes', Journal of Molecular and Cellular Cardiology, vol. 48, no. 1, pp. 261-269. https://doi.org/10.1016/j.yjmcc.2009.04.017
Kaufmann, Susann G. ; Westenbroek, Ruth E. ; Zechner, Christoph ; Maass, Alexander H. ; Bischoff, Sebastian ; Muck, Jenny ; Wischmeyer, Erhard ; Scheuer, Todd ; Maier, Sebastian K.G. / Functional protein expression of multiple sodium channel α- and β-subunit isoforms in neonatal cardiomyocytes. In: Journal of Molecular and Cellular Cardiology. 2010 ; Vol. 48, No. 1. pp. 261-269.
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