Matured hiPSC-derived cardiomyocytes possess dematuration plasticity

Human induced Pluripotent Stem Cell-derived cardiomyocytes (hiPSC-CMs) are increasingly used to identify potential factors capable of inducing endogenous cardiomyocyte proliferation to regenerate the injured heart. L-type calcium channel blockers have previously been identified as a class of factors capable of inducing matured hiPSC-CMs to proliferate. However, the mechanism by which L-type calcium channel blockers promote hiPSC-CM proliferation remains unclear. Here we provide evidence that matured hiPSC-CMs possess plasticity to undergo dematuration in response to certain pharmacological compounds. Consistent with primary cardiomyocyte maturation during perinatal development, we found that centrosome disassembly occurs in hiPSC-CMs during plate-based, temporal, maturation. A small molecule screen identified nitrendipine, an L-type calcium channel blocker, and 1-NA-PP1, a Src kinase inhibitor, as factors capable of inducing centrosome reassembly in a subpopulation of hiPSC-CMs. Furthermore, centrosome-positive hiPSC-CMs were more likely to exhibit cell cycle activity than centrosome-negative hiPSC-CMs. In contrast, neither nitrendipine or 1-NA-PP1 induced centrosome reassembly, or cell cycle activity, in neonatal rat ventricular myocytes (NRVMs). Differential bulk transcriptome analysis indicated that matured hiPSC-CMs, but not NRVMs, treated with nitrendipine or 1-NA-PP1 undergo dematuration. ScRNA transcriptome analysis supported that matured hiPSC-CMs treated with either nitrendipine or 1-NA-PP1 undergo dematuration. Collectively, our results indicate that matured hiPSC-CMs, but not primary NRVMs, possess plasticity to undergo dematuration in response to certain pharmacological compounds such as L-type calcium channel blockers and Src-kinase inhibitors. This study shows that once mature, hiPSC-CMs may not maintain their maturity under experimental conditions which may have implications for experimental systems where the state of hiPSC-CM maturation is relevant.

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Publication Details

Journal
Journal of Molecular and Cellular Cardiology Plus
Published
2025-04-01
DOI
https://doi.org/10.1016/j.jmccpl.2025.100295
Citations
3
Primary Topic
Pluripotent Stem Cells Research
Type
article
Field-Weighted Citation Impact
2.42

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article

Matured hiPSC-derived cardiomyocytes possess dematuration plasticity

Henrik Andersson, Anna Walentinsson, Daniela Später, Ruofan Wei et al.
3 citations
Journal of Molecular and Cellular Cardiology Plus
Pluripotent Stem Cells Research
2.42
article

Matured hiPSC-derived cardiomyocytes possess dematuration plasticity

Henrik Andersson, Anna Walentinsson, Daniela Später, Ruofan Wei, Alejandro Hidalgo, Ellen Poon, Maxwell Kwok, David C. Zebrowski, Frederik Adam Bjerre, Ditte Caroline Andersen, Yen Chin Hui, Meng Fang, Qing‐Dong Wang
article en
3 citations

Abstract

Human induced Pluripotent Stem Cell-derived cardiomyocytes (hiPSC-CMs) are increasingly used to identify potential factors capable of inducing endogenous cardiomyocyte proliferation to regenerate the injured heart. L-type calcium channel blockers have previously been identified as a class of factors capable of inducing matured hiPSC-CMs to proliferate. However, the mechanism by which L-type calcium channel blockers promote hiPSC-CM proliferation remains unclear. Here we provide evidence that matured hiPSC-CMs possess plasticity to undergo dematuration in response to certain pharmacological compounds. Consistent with primary cardiomyocyte maturation during perinatal development, we found that centrosome disassembly occurs in hiPSC-CMs during plate-based, temporal, maturation. A small molecule screen identified nitrendipine, an L-type calcium channel blocker, and 1-NA-PP1, a Src kinase inhibitor, as factors capable of inducing centrosome reassembly in a subpopulation of hiPSC-CMs. Furthermore, centrosome-positive hiPSC-CMs were more likely to exhibit cell cycle activity than centrosome-negative hiPSC-CMs. In contrast, neither nitrendipine or 1-NA-PP1 induced centrosome reassembly, or cell cycle activity, in neonatal rat ventricular myocytes (NRVMs). Differential bulk transcriptome analysis indicated that matured hiPSC-CMs, but not NRVMs, treated with nitrendipine or 1-NA-PP1 undergo dematuration. ScRNA transcriptome analysis supported that matured hiPSC-CMs treated with either nitrendipine or 1-NA-PP1 undergo dematuration. Collectively, our results indicate that matured hiPSC-CMs, but not primary NRVMs, possess plasticity to undergo dematuration in response to certain pharmacological compounds such as L-type calcium channel blockers and Src-kinase inhibitors. This study shows that once mature, hiPSC-CMs may not maintain their maturity under experimental conditions which may have implications for experimental systems where the state of hiPSC-CM maturation is relevant.

Journal of Molecular and Cellular Cardiology PlusVol. 12
The University of Melbourne (AU), Chinese University of Hong Kong (HK), University of Southern Denmark (DK), Odense University Hospital (DK), Karolinska Institutet (SE), Integrated Cardio Metabolic Centre (SE), Gen-9 (United States) (US), AstraZeneca (Sweden) (SE), Murdoch Children's Research Institute (AU), New York University (US)
AstraZeneca, Lundbeckfonden, Novo Nordisk, Odense Universitetshospital, Chinese University of Hong Kong, Novo Nordisk Fonden, H. Lundbeck A/S, Health and Medical Research Fund
Zero hunger
Openalex Percentile: Top 12%
Pluripotent Stem Cells Research
2.42
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