European heart journal · 2025
SCN10A-short gene therapy to restore conduction and protect against malignant cardiac arrhythmias.
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Wang Jianan, Verkerk Arie O, Wilders Ronald, Zhang Yingnan, Zhang Kelly, Prakosa Adityo, Rivaud Mathilde R, Marsman E Madelief J, Boender Arie R, Klerk Mischa, Fokkert Lianne, de Jonge Berend, Neef Klaus, Kirzner Osne F, Bezzina Connie R, Remme Carol Ann, Tan Hanno L, Boukens Bastiaan J, Devalla Harsha D, Trayanova Natalia A, Christoffels Vincent M, Barnett Phil, Boink Gerard J J
Аннотация
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 treat cardiac conduction abnormalities and associated 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 treat cardiac conduction abnormalities and associated arrhythmias.