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Highlights • Ion channel gene expression changes extensively as hPSC-CM grafts mature in vivo • Targeting individual ion channels was insufficient to prevent engraftment arrhythmia • Automaticity of hPSC-CMs relies on calcium and voltage clocks • Graft automaticity is a major contributor to arrhythmias post-hPSC-CM engraftment Summary Human pluripotent stem cell-derived cardiomyocytes (hPSC-CMs) offer a promising cell-based therapy for myocardial infarction.
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