Mohamed-Yassine Amarouch
Elena V. Zaklyazminskaya
Jean-Sébastien Rougier- 1R.N.E Laboratory, Multidisciplinary Faculty of Taza, University Sidi Mohamed Ben Abdellah, Fez, Morocco
- 2Medical Genetics Laboratory, Petrovsky National Research Centre of Surgery, Moscow, Russia
- 3Institute of Biochemistry and Molecular Medicine, University of Bern, Bern, Switzerland
Editorial on the Research Topic
Inherited Arrhythmias of the Cardiac Sodium Channel Nav1.5
Ion channels are pore-forming transmembrane proteins involved in the transport of ions across cell membranes according to their electrochemical gradients. In cardiomyocytes, the activity of these proteins maintains the resting membrane potential and generates action potentials. Thereby, ion channels play a key role in the excitability of the heart.
Ion channel dysfunction is linked with a broad range of inherited arrhythmias that may lead to sudden cardiac death. These disorders are formerly known as channelopathies and are commonly associated with the presence of mutations in genes encoding cardiac ion channels and/or their interacting proteins (Skinner et al., 2019). As a consequence, functional alterations or mislocalization of ion channels or their regulatory proteins might deeply affect the action potential and promote life-threatening ventricular arrhythmias through changes in intracellular calcium handling (Landstrom et al., 2017).
In the heart, Nav1.5 represents the preponderant isoform of the voltage-gated sodium channels. It is responsible for the fast-initial depolarization phase of action potential and as such represents a critical determinant of the excitability and conduction of the electrical impulse through the myocardium. Therefore, Nav1.5 dysfunction has been linked with several inherited cardiac arrhythmias. On the one hand, a gain-of-function mutations of the SCN5A gene, which encodes the α-subunit of Nav1.5, are associated with the congenital long QT syndrome, atrial fibrillation, multifocal ectopic Purkinje-related premature contractions, and exercise-induced polymorphic ventricular tachycardia (Amarouch and Abriel, 2015; Verkerk et al., 2018). On the other hand, loss-of-function mutations of this channel are linked with Brugada Syndrome (BrS), sick sinus syndrome, and cardiac conduction diseases (Verkerk et al., 2018). Moreover, Nav1.5 malfunction may also lead to structural heart diseases such as dilated cardiomyopathy and arrhythmogenic right ventricular cardiomyopathy/dysplasia (Verkerk et al., 2018; Jordan et al., 2021).
The purpose of this Frontiers Research Topic on inherited arrhythmias of the cardiac sodium channel Nav1.5 is to present recent findings, leading us to have a better understanding of the cardiac sodium channel physiology, and highlighting the pathophysiological mechanisms underlying arrhythmias related to cardiac sodium channelopathies. These investigations can contribute significantly to improving decision-making along the whole patient pathway by targeting the biological effects of the disease-causing mutations.
In this Frontiers Research Topic Dong et al. provide a review on the life cycle of the cardiac voltage-gated sodium channel Nav1.5. These authors focused on the different phases of the Nav1.5 life cycle and summarized SCN5A-related diseases and novel therapeutic strategies targeting Nav1.5.
Tse et al. present a territory-wide study from Hong Kong and analyzed the genetic composition of BrS patients, who underwent genetic testing over a 21-year period. For this purpose, a total of 65 patients were included and analyzed retrospectively. This study identifies six novel variants in the SCN5A gene, which have not been reported in cohorts outside of the Hong Kong region.
Regarding original research articles, Hichri et al. developed a novel computational approach to address an important topic related to a recent finding in the field of sodium channel biophysics. Clatot et al. (2017) report that sodium channels, including Nav1.5, act as a dimer. Their α-subunits interact physically with each other via the cytoplasmic protein 14-3-3, leading to coupled channel gating. These findings strongly suggest that sodium channels operate and gate as dimers rather than non-interacting entities. In this context, Hichri et al. developed a novel approach, integrating the notion of sodium channel dimer as the functional unit of the sodium current. The authors investigated whether the newly identified channel-channel interactions can contribute to the negative dominant effect of cardiac sodium channel variants such as Nav1.5-p.L325R. The simulation results suggest that interactions with the variant channel may contribute to the negative-dominant effect.
In the same context, Zheng et al. investigate the dominant negative effect mechanisms produced by the SCN5A splice variant E28D. This variant results in the truncated sodium channel Nav1.5-p.G1642X, which is significantly upregulated in human Heart Failure (HF). These authors demonstrate that the Nav1.5-p.G1642X channel interacts with the WT-Nav1.5 and thereby exerts a dominant-negative effect, contributing to the decrease in INa seen in HF. Furthermore, Zheng et al. show that the sodium channel polymorphism p.H558R can rescue the loss-of-function related to the Nav1.5-p.G1642X dominant-negative effect by impairing the biophysical coupling between the splice variant and the WT channel.
Also related to the same topic, Doisne et al. investigate the dominant-negative effect of the BrS Nav1.5-p.R104W variant in a murine model using adeno-associated viruses. The cardiac sodium current of p.R104W injected mice was significantly decreased. Moreover, the overexpression of this variant in normal hearts led to a decreased expression of Nav1.5. Altogether, these results demonstrated an in-vivo dominant-negative effect of Nav1.5-p.R104W channels on the endogenous ones.
Finally, Ghovanloo et al. characterize a novel SCN5A variant, p.T1857I, identified in a family with a CPVT-like phenotype, and located in the C-terminus of Nav1.5. The functional characterization of Nav1.5-p.T1857I revealed significant positive shifts in voltage-dependences of both activation and inactivation. Moreover, a delayed recovery from fast inactivation was observed in the mutated condition, while action potential simulations suggest the occurrence of ventricular after depolarization, predisposing carriers to cardiac arrhythmias.
Conclusion
This Research Topic underscores the pathophysiological implications of rare SCN5A variants in cardiac arrhythmia. Many of the published studies highlight the molecular complexity underlying the effect of some rare SCN5A variants, especially the contribution of the newly identified α-α subunit interactions to Nav1.5 gating and the negative dominant effect.
Author Contributions
M-YA, EZ, and J-SR have made a direct contribution to the work and approved it for publication. All authors contributed to the article and approved the submitted version.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher's Note
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References
Amarouch, M. Y., and Abriel, H. (2015). Cellular hyper-excitability caused by mutations that alter the activation process of voltage-gated sodium channels. Front. Physiol. 6:45. doi: 10.3389/fphys.2015.00045
Clatot, J., Hoshi, M., Wan, X., Liu, H., Jain, A., Shinlapawittayatorn, K., et al. (2017). Voltage-gated sodium channels assemble and gate as dimers. Nat. Commun. 8:2077. doi: 10.1038/s41467-017-02262-0
Jordan, E., Peterson, L., Ai, T., Asatryan, B., Bronicki, L., Brown, E., et al. (2021). An evidence-based assessment of genes in dilated cardiomyopathy. Circulation 144, 7–19. doi: 10.1161/CIRCULATIONAHA.120.053033
Landstrom, A. P., Dobrev, D., and Wehrens, X. H. T. (2017). Calcium signaling and cardiac arrhythmias. Circ. Res. 120, 1969–1993. doi: 10.1161/CIRCRESAHA.117.310083
Skinner, J. R., Winbo, A., Abrams, D., Vohra, J., and Wilde, A. A. (2019). Channelopathies that lead to sudden cardiac death: clinical and genetic aspects. Heart Lung Circ. 28, 22–30. doi: 10.1016/j.hlc.2018.09.007
Keywords: cardiac channelopathies, electrophysiology, inherited arrhythmias, SCN5A, Nav1.5
Citation: Amarouch M-Y, Zaklyazminskaya EV and Rougier J-S (2021) Editorial: Inherited Arrhythmias of the Cardiac Sodium Channel Nav1.5. Front. Physiol. 12:716553. doi: 10.3389/fphys.2021.716553
Received: 28 May 2021; Accepted: 04 June 2021;
Published: 04 August 2021.
Edited and reviewed by: Ruben Coronel, University of Amsterdam, Netherlands
Copyright © 2021 Amarouch, Zaklyazminskaya and Rougier. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Mohamed-Yassine Amarouch, bW9oYW1lZC5hbWFyb3VjaCYjeDAwMDQwO3VzbWJhLmFjLm1h