The effect of reactive oxygen species on cardiomyocyte differentiation of pluripotent stem cells
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Updated: Feb 16, 2026

Differentiation of Atrial Cardiomyocytes from Pluripotent Stem Cells Using the BMP Antagonist Grem2
Published on: March 10, 2016
1a Cardiac Signaling Center of University of South Carolina, Medical University of South Carolina and Clemson University , Charleston , SC , USA.
Abstract:
The coordination of metabolic shift with genetic circuits is critical to cell specification, but the metabolic mechanisms that drive cardiac development are largely unknown. Reactive oxygen species (ROS) are not only the by-product of mitochondrial metabolism, but play a critical role in signalling cascade of cardiac development as a second messenger. Various levels of ROS appear differential and even oppose effect on selfrenewal and cardiac differentiation of pluripotent stem cells (PSCs) at each stage of differentiation. The intracellular ROS and redox balance are meticulous regulated by several systems of ROS generation and scavenging, among which mitochondria and the NADPH oxidase (NOX) are major sources of intracellular ROS involved in cardiomyocyte differentiation. Some critical signalling modulators are activated or inactivated by oxidation, suggesting ROS can be involved in regulation of cell fate through these downstream targets. In this review, the literatures about major sources of ROS, the effect of ROS level on cardiac differentiation of PSCs, as well as the underlying mechanism of ROS in the control of cardiac fate of PSC are summarised and discussed.
Insights
Reactive oxygen species (ROS) are crucial signaling molecules in cardiac development. This review explores how ROS levels and sources impact pluripotent stem cell differentiation into cardiomyocytes.
Area of Science:
- Cardiovascular Biology
- Stem Cell Biology
- Metabolic Signaling
Background:
- Metabolic shifts are vital for cell specification, yet cardiac development mechanisms remain unclear.
- Reactive oxygen species (ROS), a byproduct of metabolism, act as signaling molecules in cardiac development.
- ROS levels differentially affect pluripotent stem cell (PSC) self-renewal and cardiac differentiation.
Purpose of the Study:
- To review the literature on ROS generation and scavenging systems.
- To discuss the impact of varying ROS levels on PSC cardiac differentiation.
- To elucidate the mechanisms by which ROS regulate cardiac cell fate.
Main Methods:
- Literature review and synthesis.
- Analysis of ROS generation sources (mitochondria, NADPH oxidase).
- Examination of ROS effects on PSCs during differentiation.
Main Results:
- Mitochondria and NADPH oxidase are key intracellular ROS sources in cardiomyocyte differentiation.
- ROS levels critically influence PSC self-renewal and differentiation.
- Oxidation by ROS modulates signaling pathways, affecting cell fate.
Conclusions:
- ROS play a significant role in regulating cardiac development through signaling cascades.
- Understanding ROS dynamics is essential for controlling PSC differentiation into cardiomyocytes.
- Further research into ROS mechanisms can advance cardiac regenerative medicine.
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