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bioRxiv · 10.1101/2025.05.19.654350

Selectivity filter mutation in NaV1.5 promotes ventricular tachycardia

Abstract

Loss-of-Function (LoF) mutations in the SCN5A gene, which encodes for the predominant cardiac NaV isoform, NaV1.5 result in either deficiency in the channel expression or function. Impaired NaV1.5 expression and function underlie reduced peak Na+ current (INa) and result in ventricular conduction velocity slowing, predisposing the heart to conduction block and ventricular arrhythmias clinically associated with Brugada syndrome (BrS). Recently, a missense mutation in NaV1.5 selectivity filter (DEKA motif), K1419E (DEEA) has been identified in patients with BrS. Despite early characterization of mutations in selectivity filter of other NaV isoforms, little is known about the impact of DEEA on NaV1.5 function as well as on cardiac electrophysiology. Therefore, we generated a mouse heterozygous for NaV1.5 DEEA to characterize the mutation and investigate the outcome of this functionally deficient NaV1.5 variant on cardiac electrophysiology and arrhythmias. Heterologous expression system and isolated cardiomyocytes revealed lower current density and unchanged NaV1.5 expression in DEEA vs. wild type (DEKA). On the organ level, optical mapping revealed conduction velocity slowing in DEEA hearts, which was accentuated by flecainide resulting in vivo ventricular arrhythmias. Overall, to our knowledge, we provide the first mechanistic insight into the proarrhythmic consequences of a functionally deficient BrS mutation in NaV1.5. Condensed abstractNaV1.5 mutations have been associated with life-threatening arrhythmias. Recently, a selectivity filter mutation (K1419E-NaV1.5, DEKA[->]DEEA), has been linked to Brugada Syndrome (BrS). While DEKA mutations in other NaV isoforms affected channel conductance, the impact of DEEA on NaV1.5 and arrhythmogenesis is unknown. Therefore, we generated mice heterozygous for NaV1.5-DEEA. Cardiomyocytes isolated from DEEA hearts exhibited substantial reduction in sodium current, ventricular conduction slowing and susceptibility to ventricular arrhythmias in vivo that were unmasked by flecainide. Together, DEEA murine model is the first to recapitulate a functional deficiency in NaV1.5, and thus offers insight into the proarrhythmic mechanism of BrS.

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Selimi, Z., Tarasov, M., Meng, X., Dias, P., Moise, B., Veeraraghavan, R., Radwanski, P.. 2025-05-24. Selectivity filter mutation in NaV1.5 promotes ventricular tachycardia. https://doi.org/10.1101/2025.05.19.654350

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