SCN10A-short gene therapy to restore conduction and protect against malignant cardiac arrhythmias

作者：Jianan Wang, Arie O. Verkerk, Ronald Wilders, Yingnan Zhang, Kelly Zhang, Adityo Prakosa, Mathilde R. Rivaud, E Madelief J Marsman, Arnie Boender, Mischa Klerk, Lianne Fokkert, Berend de Jonge, Klaus Neef, osne kirzner, Connie R. Bezzina, Carol Ann Remme, Hanno L. Tan, Bastiaan J. Boukens, Harsha D. Devalla, Natalia A. Trayanova, Vincent M. Christoffels, Phil Barnett, Gerard J.J. Boink · 发表于：European Heart Journal · 年份：2025 · DOI：10.1093/eurheartj/ehaf053 · 被引用次数：17 · 研究领域：Cardiac electrophysiology and arrhythmias、Ion channel regulation and function、Pluripotent Stem Cells Research

BACKGROUND AND AIMS: Life-threatening arrhythmias are a well-established consequence of reduced cardiac sodium current (INa). Gene therapy approaches to increase INa have demonstrated potential benefits to prevent arrhythmias. However, the development of such therapies is hampered by the large size of sodium channels. In this study, SCN10A-short (S10s), a short transcript encoding the carboxy-terminal domain of the human neuronal sodium channel, was evaluated as a gene therapy target to increase INa and prevent arrhythmias. METHODS: Adeno-associated viral vector overexpressing S10s was injected into wild type and Scn5a-haploinsufficient mice on which patch-clamp studies, optical mapping, electrocardiogram analyses, and ischaemia reperfusion were performed. In vitro and in silico studies were conducted to further explore the effect of S10s gene therapy in the context of human hearts. RESULTS: Cardiac S10s overexpression increased cellular INa, maximal action potential upstroke velocity, and action potential amplitude in Scn5a-haploinsufficient cardiomyocytes. S10s gene therapy rescues conduction slowing in Scn5a-haploinsufficient mice and prevented ventricular tachycardia induced by ischaemia-reperfusion in wild type mice. S10s overexpression increased maximal action potential upstroke velocity in human inducible pluripotent stem cell-derived cardiomyocytes and prevented inducible arrhythmias in simulated human heart models. CONCLUSIONS: S10s gene therapy may be effective to t...