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Updated: Nov 6, 2025

Assessing Cardiomyocyte Subtypes Following Transcription Factor-mediated Reprogramming of Mouse Embryonic Fibroblasts
Published on: March 22, 2017
Maturing heart muscle cells: Mechanisms and transcriptomic insights
Sean A Murphy1, Elaine Zhelan Chen2, Leslie Tung2
1Division of Cardiology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA; Department of Biomedical Engineering, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA; Department of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA; Institute of Cell Engineering, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA; Cellular and Molecular Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Generating mature cardiomyocytes (CMs) from stem cells remains challenging. This review explores CM maturation, transcriptional regulation, and biomimetic strategies to improve stem cell-derived CMs for biomedical use.
Area of Science:
- Cardiovascular Biology
- Stem Cell Biology
- Developmental Biology
Background:
- Cardiomyocyte (CM) maturation is a complex process transforming fetal CMs into adult CMs.
- Pluripotent stem cell-derived CMs (PSC-CMs) exhibit incomplete maturation in culture, limiting their applications.
- Significant research efforts focus on achieving mature PSC-CMs.
Purpose of the Study:
- To review key aspects of native CM maturation.
- To discuss recent findings on factors and mechanisms regulating CM maturation.
- To explore biomimetic strategies for enhancing PSC-CM maturation.
Main Methods:
- Review of existing literature on cardiomyocyte maturation.
- Emphasis on transcriptional regulation and gene expression analysis.
- Discussion of single-cell RNA-sequencing (scRNA-seq) as a tool for studying maturation.
- Analysis of biomimetic strategies and their effects.
Main Results:
- Maturation involves significant changes in CM morphology, function, metabolism, and transcriptome.
- Transcriptional regulation plays a critical role in controlling CM maturation.
- scRNA-seq is instrumental in analyzing time-series gene regulation and maturation states.
- Biomimetic strategies show promise in improving PSC-CM maturation.
Conclusions:
- Understanding CM maturation is crucial for advancing regenerative medicine.
- Targeting transcriptional regulation and employing biomimetic approaches can enhance PSC-CM maturation.
- Mature PSC-CMs hold significant potential for biomedical applications, including disease modeling and cell therapy.
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