bioRxivPhysiologyPreprint
AAV6-HCN4t-mediated biological pacing as a potential life-saving therapy for congenital complete heart block
Jianan WangiD, Evelien E. BirzaiD, Veronique M.F. MeijborgiD, Arie O. VerkerkiD, Aina Cervera-BareaiD, Timo JonkeriD, Ruud N. VisseriD, Rinske SparriusiD, Mischa KlerkiD, Arnie BoenderiD, Yuting Yang, Emiel J.M. Kramer, Ganghyun Kwak, Kyungho ParkiD, Larry C. ParkiD, Joyce Visser, Marlijn S. Jansen, Silke SchrödeliD, Mudit MishraiD, Christian ThirioniD, Joost P. G. SluijteriD, Saskia C.A. de JageriD, Klaus NeefiD, Nico A. BlomiD, Monique C. HaakiD, , Gerard J.J. BoinkiD
- Citations
- 0
Abstract
Congenital complete heart block (CCHB) is a life-threatening condition in fetuses due to severe bradycardia. Maternal administration of {beta}-adrenergic agonists is used to increase fetal heart rates, but its effectiveness is limited and lost over time most likely due to insufficient expression of HCN channels in some individuals. We report the development of an injectable gene therapy that produces reliable cardiac pacemaker function in the presence of {beta}-adrenergic stimulation. Intramyocardial injection of adeno-associated viral serotype 6 vectors expressing HCN4t (AAV6-HCN4t) into the left ventricular apex significantly increased ectopic pacing frequency and heart rate in response to isoproterenol in rats with complete heart block, and this effect remained stable throughout the 4 weeks of follow-up. Injection of AAV6-HCN4t showed similar reliable biological pacing in complete heart block pigs. These results suggest that AAV6-HCN4t generates robust biological pacing in the presence of isoproterenol, providing the foundation for a potentially life-saving therapy for in utero CCHB.
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Human pluripotent stem cell-derived atrioventricular node-like pacemaker cells exhibit biological conduction bridge properties in vitro and in vivo
Michelle Lohbihler, Amos A. Lim, … Stephanie I. Protze·bioRxiv·Sep 4, 2025
- Adeno-associated virus (AAV)-TBX18 does not generate biological pacemaker activity, unlike AAV-Hcn2
Jianan Wang, Mathilde R. Rivaud, … Gerard J.J. Boink·Journal of Clinical InvestigationPeer-reviewed·Jun 11, 2026
- Thermogenetics for cardiac pacing
Alexander V. Balatskiy, Alexey M. Nesterenko, … Vsevolod Vadimovich Belousov·bioRxiv·Jan 2, 2024
- Control of cytokinesis by β-adrenergic receptors indicates an approach for regulating cardiomyocyte endowment
H. Liu, C.-H. Zhang, … B. Kuhn·bioRxiv·Oct 4, 2019
- Cav1.3-C-terminus Restores Electrical and Contractile Functions in hiPSC-derived Cardiomyocytes Model of Heart Failure
Yvonne Sleiman, Jean‐Baptiste Reisqs, Mohamed Boutjdir·bioRxiv·Oct 28, 2026
- Pharmacologic Therapy for Engraftment Arrhythmia Induced by Transplantation of Human Cardiomyocytes
K. Nakamura, L. E. Neidig, … C. E. Murry·Stem Cell ReportsPeer-reviewed·Oct 1, 2021