# Unraveling the Complex Cellular Repair Mechanisms Following Myocardial Infarction

**Authors:** Ruiling Chen, Yalin Fu, Ling Hu, Yuqing Chen, Pengyun Li

PMC · DOI: 10.3390/ijms26136002 · International Journal of Molecular Sciences · 2025-06-23

## TL;DR

This paper reviews how different heart cells help repair damage after a heart attack and explores new cell-based treatments for improving recovery.

## Contribution

The paper provides novel insights into the regenerative roles of non-cardiac and cardiac cells in myocardial infarction repair and emphasizes the need for age-specific therapeutic strategies.

## Key findings

- Non-cardiac stem cells and cardiac cells contribute to MI repair through proliferation, angiogenesis, and immune regulation.
- Cell-based therapies show potential for preventing heart failure post-MI but require age-specific strategies for efficacy.
- The review highlights the complex mechanisms of MI repair and the translational potential of cell-based approaches.

## Abstract

Growing evidence underscores the pivotal roles of both in situ-resident and -non-resident cardiac cells in the repair mechanisms following myocardial infarction (MI). MI continues to be a predominant cause of death and disability, posing a significant threat to global health and well-being. Despite advances in medical care, current therapies remain insufficient in preventing ventricular remodeling and heart failure post-MI. We seek to clarify the underlying regenerative mechanisms by which distinct cell types contribute to the repair of MI injury and to systematically assess the translational potential and therapeutic efficacy of these cell-based approaches in clinical applications. This review conducts a comprehensive analysis of recent research progress on the roles of non-cardiac stem cells in situ and cardiac cells derived from explants in MI repair. These cells contribute to the repair process through multiple mechanisms, including cell proliferation and differentiation, angiogenesis, paracrine signaling, immune regulation and fibrosis modulation. Our analysis reveals the intricate mechanisms of MI repair and highlights the necessity for developing age-specific therapeutic strategies for certain cell types. This review offers novel insights into cell-based treatment for MI and provides a scientific foundation for future clinical trials of cardiac regenerative medicine.

## Linked entities

- **Diseases:** myocardial infarction (MONDO:0005068), heart failure (MONDO:0005252)

## Full-text entities

- **Diseases:** ventricular remodeling (MESH:D020257), death (MESH:D003643), MI (MESH:D009203), fibrosis (MESH:D005355), heart failure (MESH:D006333)

## Full text

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## Figures

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## References

108 references — full list in the complete paper: https://tomesphere.com/paper/PMC12249660/full.md

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Source: https://tomesphere.com/paper/PMC12249660