Characterization of sodium channel alpha- and beta-subunits in rat and mouse cardiac myocytes
- PMID: 11238277
- DOI: 10.1161/01.cir.103.9.1303
Characterization of sodium channel alpha- and beta-subunits in rat and mouse cardiac myocytes
Abstract
Background: Sodium channels isolated from mammalian brain are composed of alpha-, beta(1)-, and beta(2)-subunits. The composition of sodium channels in cardiac muscle, however, has not been defined, and disagreement exists over which beta-subunits are expressed in the myocytes. Some investigators have demonstrated beta(1) expression in heart. Others have not detected any auxiliary subunits. On the basis of Northern blot analysis of total RNA, beta(2) expression has been thought to be exclusive to neurons and absent from cardiac muscle.
Methods and results: The goal of this study was to define the subunit composition of cardiac sodium channels in myocytes. We show that cardiac sodium channels are composed of alpha-, beta(1)-, and beta(2)-subunits. Nav1.5 and Nav1.1 are expressed in myocytes and are associated with beta(1)- and beta(2)-subunits. Immunocytochemical localization of Nav1.1, beta(1), and beta(2) in adult heart sections showed that these subunits are expressed at the Z lines, as shown previously for Nav1.5. Coexpression of Nav1.5 with beta(2) in transfected cells resulted in no detectable changes in sodium current.
Conclusions: Cardiac sodium channels are composed of alpha- (Nav1.1 or Nav1.5), beta(1)-, and beta(2)-subunits. Although beta(1)-subunits modulate cardiac sodium channel current, beta(2)-subunit function in heart may be limited to cell adhesion.
Similar articles
-
Distribution and function of sodium channel subtypes in human atrial myocardium.J Mol Cell Cardiol. 2013 Aug;61:133-141. doi: 10.1016/j.yjmcc.2013.05.006. Epub 2013 May 20. J Mol Cell Cardiol. 2013. PMID: 23702286 Free PMC article.
-
Molecular differential expression of voltage-gated sodium channel α and β subunit mRNAs in five different mammalian cell lines.J Bioenerg Biomembr. 2011 Dec;43(6):729-38. doi: 10.1007/s10863-011-9399-7. Epub 2011 Nov 12. J Bioenerg Biomembr. 2011. PMID: 22081212
-
Sodium channel beta4, a new disulfide-linked auxiliary subunit with similarity to beta2.J Neurosci. 2003 Aug 20;23(20):7577-85. doi: 10.1523/JNEUROSCI.23-20-07577.2003. J Neurosci. 2003. PMID: 12930796 Free PMC article.
-
Sodium channel beta subunits: anything but auxiliary.Neuroscientist. 2001 Feb;7(1):42-54. doi: 10.1177/107385840100700108. Neuroscientist. 2001. PMID: 11486343 Review.
-
Beta subunits: players in neuronal hyperexcitability?Novartis Found Symp. 2002;241:124-38; discussion 138-43, 226-32. Novartis Found Symp. 2002. PMID: 11771642 Review.
Cited by
-
Cardiac arrhythmia in a mouse model of sodium channel SCN8A epileptic encephalopathy.Proc Natl Acad Sci U S A. 2016 Nov 8;113(45):12838-12843. doi: 10.1073/pnas.1612746113. Epub 2016 Oct 26. Proc Natl Acad Sci U S A. 2016. PMID: 27791149 Free PMC article.
-
Fhf2 gene deletion causes temperature-sensitive cardiac conduction failure.Nat Commun. 2016 Oct 4;7:12966. doi: 10.1038/ncomms12966. Nat Commun. 2016. PMID: 27701382 Free PMC article.
-
Sinus node dysfunction following targeted disruption of the murine cardiac sodium channel gene Scn5a.J Physiol. 2005 Sep 1;567(Pt 2):387-400. doi: 10.1113/jphysiol.2005.083188. Epub 2005 Jun 2. J Physiol. 2005. PMID: 15932895 Free PMC article.
-
The dispensability of 14-3-3 proteins for the regulation of human cardiac sodium channel Nav1.5.PLoS One. 2024 Mar 7;19(3):e0298820. doi: 10.1371/journal.pone.0298820. eCollection 2024. PLoS One. 2024. PMID: 38452156 Free PMC article.
-
The Kir2.1E299V mutation increases atrial fibrillation vulnerability while protecting the ventricles against arrhythmias in a mouse model of short QT syndrome type 3.Cardiovasc Res. 2024 Apr 30;120(5):490-505. doi: 10.1093/cvr/cvae019. Cardiovasc Res. 2024. PMID: 38261726 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Molecular Biology Databases