Signaling mechanisms and dynamics governing the myocardial-epicardial fate switch during human cardiogenesis

The signaling mechanisms and developmental dynamics that govern the divergence of myocardial and epicardial lineages during human heart development remain poorly understood. Here, we developed a human pluripotent stem cell-based cardiac development model and employed time-course single-cell RNA sequencing to delineate cardiac lineage specification trajectories. We identified retinoic acid (RA) as a critical fate switch at the cardiac mesoderm stage. RA instructs epicardial lineage commitment of cardiac mesoderm through a primed-epicardium to proepicardium-like population and finally to epicardium, a process requiring precise BMP modulation. Conversely, RA absence directs cardiac mesoderm along a default myocardial pathway, yielding developing and mature cardiomyocytes. Both trajectories are governed by the hierarchical activation of key transcription factors. Our study integrates signaling and dynamics to elucidate the temporal regulatory network of the RA-BMP axis in human cardiac fate determination. These findings provide fundamental insights into human cardiogenesis and a crucial roadmap for modeling heart disease and advancing regenerative strategies.

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Publication Details

Journal
Science Advances
Published
2026-07-24
DOI
https://doi.org/10.1126/sciadv.aee5316
Primary Topic
Congenital heart defects research
Type
article
Field-Weighted Citation Impact
0.00

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article

Signaling mechanisms and dynamics governing the myocardial-epicardial fate switch during human cardiogenesis

Ruize Kong, Zongyong Ai, Tianqing Li, D Wang et al.
Science Advances
Congenital heart defects research
article

Signaling mechanisms and dynamics governing the myocardial-epicardial fate switch during human cardiogenesis

Ruize Kong, Zongyong Ai, Tianqing Li, D Wang, Yu Yin, Xiaobo Wang, C J Li, Zhenlin Liu, Baohua Niu, Min Zhou
article en

Abstract

The signaling mechanisms and developmental dynamics that govern the divergence of myocardial and epicardial lineages during human heart development remain poorly understood. Here, we developed a human pluripotent stem cell-based cardiac development model and employed time-course single-cell RNA sequencing to delineate cardiac lineage specification trajectories. We identified retinoic acid (RA) as a critical fate switch at the cardiac mesoderm stage. RA instructs epicardial lineage commitment of cardiac mesoderm through a primed-epicardium to proepicardium-like population and finally to epicardium, a process requiring precise BMP modulation. Conversely, RA absence directs cardiac mesoderm along a default myocardial pathway, yielding developing and mature cardiomyocytes. Both trajectories are governed by the hierarchical activation of key transcription factors. Our study integrates signaling and dynamics to elucidate the temporal regulatory network of the RA-BMP axis in human cardiac fate determination. These findings provide fundamental insights into human cardiogenesis and a crucial roadmap for modeling heart disease and advancing regenerative strategies.

Science AdvancesVol. 12(30)
Kunming University of Science and Technology (CN), First People's Hospital of Yunnan Province (CN), The First Hospital of Kunming (CN), Yunnan Yingmao Biotechnology (China) (CN), Dali University (CN)
National Natural Science Foundation of China
Good health and well-being
Openalex Percentile: Top 14%
Congenital heart defects research
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Signaling mechanisms and dynamics governing the myocardial-epicardial fate switch during human cardiogenesis — Ruize Kong, Zongyong Ai, et al. · Science Advances (2026) | TGRS Research Map | TGRS