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Updated: Apr 6, 2026

In Vitro Model of Coronary Angiogenesis
Published on: March 10, 2020
Hematopoietic progenitors are required for proper development of coronary vasculature
Gentian Lluri1, Vincent Huang2, Marlin Touma3
1Department of Molecular Cell and Developmental Biology, University of California, Los Angeles, Los Angeles, CA 90095, USA; Department of Medicine, Section of Cardiology, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Insights
Hematopoietic cells are crucial for coronary vessel development in the heart. Their absence leads to disorganized and underdeveloped coronary vasculature, suggesting a vital role in heart development.
Area of Science:
- Developmental biology
- Cardiovascular research
- Hematopoiesis
Background:
- Hematopoietic cells are present in the myocardium before coronary vessel formation.
- The specific role of these early hematopoietic cells in coronary development remains unclear.
Purpose of the Study:
- To investigate the necessity of pre-existing hematopoietic cells for coronary vasculature formation.
- To elucidate the role of hematopoietic progenitors in heart development.
Main Methods:
- Utilized Runx1 knockout and Vav1-cre; R26-DTA mouse models to create hematopoietic cell-deficient embryos.
- Performed whole-mount and section stainings to analyze coronary vasculature.
- Conducted ex vivo coronary explant experiments.
Main Results:
- Runx1 knockout and Vav1-cre; R26-DTA embryos displayed disorganized and hypoplastic coronary microvasculature.
- Ex vivo heart explants from these models showed impaired coronary formation.
- Epicardial to mesenchymal transition was negatively affected in the absence of hematopoietic progenitors.
Conclusions:
- Hematopoietic cells actively induce coronary growth, rather than being passively transported.
- These findings reveal a novel mechanism regulating coronary vascular development.
Rationale:
During embryogenesis, hematopoietic cells appear in the myocardium prior to the initiation of coronary formation. However, their role is unknown.
Objective:
Here we investigate whether pre-existing hematopoietic cells are required for the formation of coronary vasculature.
Methods And Results:
As a model of for hematopoietic cell deficient animals, we used Runx1 knockout embryos and Vav1-cre; R26-DTA embryos, latter of which genetically ablates 2/3 of CD45(+) hematopoietic cells. Both Runx1 knockout embryos and Vav1-cre; R26-DTA embryos revealed disorganized, hypoplastic microvasculature of coronary vessels on section and whole-mount stainings. Furthermore, coronary explant experiments showed that the mouse heart explants from Runx1 and Vav1-cre; R26-DTA embryos exhibited impaired coronary formation ex vivo. Interestingly, in both models it appears that epicardial to mesenchymal transition is adversely affected in the absence of hematopoietic progenitors.
Conclusion:
Hematopoietic cells are not merely passively transported via coronary vessel, but substantially involved in the induction of the coronary growth. Our findings suggest a novel mechanism of coronary growth.
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