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Updated: Jul 16, 2026

In Vitro Culture of Epicardial Cells From Mouse Embryonic Heart
Published on: April 27, 2016
The proepicardium delivers hemangioblasts but not lymphangioblasts to the developing heart
Jörg Wilting1, Kerstin Buttler, Inga Schulte
1Children's Hospital, Pediatrics I, University of Göttingen, Robert-Koch-Strasse 40, 37075 Göttingen, Germany. joerg.wilting@med.uni-goettingen.de
Insights
The proepicardium (PE) contributes to coronary blood vessels but not cardiac lymphatics. Cardiac lymphatics originate from immigrating lymphangioblasts, distinct from blood vessel origins.
Area of Science:
- Developmental biology
- Cardiovascular research
- Vascular biology
Background:
- The vertebrate heart's myocardium and endocardium originate from lateral plate mesoderm.
- The epicardium, cardiac interstitium, and coronary blood vessels arise from the proepicardium (PE).
- Cardiac lymphatics' origin remains unstudied despite their association with coronary vessels.
Purpose of the Study:
- To investigate the origin of cardiac lymphatic vessels.
- To determine if the proepicardium (PE) contributes to cardiac lymphatics.
- To elucidate the distinct origins of cardiac blood and lymph vessels.
Main Methods:
- Grafting of quail proepicardium (PE) into chick embryos.
- Double staining using quail endothelial cell (EC) marker QH1 and lymphatic endothelial marker Prox1.
- Analysis of cell populations in murine embryos using markers Lyve-1, CD31, and CD45.
Main Results:
- Quail PE contributed hemangioblasts to the chick heart but not lymphangioblasts.
- No quail endothelial cells (ECs) were observed in chick cardiac lymphatics, except for a potential lympho-venous anastomosis.
- A basal to apical gradient of specific cell markers in murine embryos suggests immigrating lymphangioblasts form cardiac lymphatics.
Conclusions:
- Coronary blood vessels and cardiac lymphatics originate from different sources.
- The proepicardium (PE) is a source for coronary blood vessel precursors but not cardiac lymphatics.
- Cardiac lymphatics develop from immigrating lymphangioblasts, growing from the base to the apex of the heart.
Abstract:
The mass of the myocardium and endocardium of the vertebrate heart derive from the heart-forming fields of the lateral plate mesoderm. Further components of the mature heart such as the epicardium, cardiac interstitium and coronary blood vessels originate from a primarily extracardiac progenitor cell population: the proepicardium (PE). The coronary blood vessels are accompanied by lymph vessels, suggesting a common origin of the two vessel types. However, the origin of cardiac lymphatics has not been studied yet. We have grafted PE of HH-stage 17 (day 3) quail embryos hetero- and homotopically into chick embryos, which were re-incubated until day 15. Double staining with the quail endothelial cell (EC) marker QH1 and the lymphendothelial marker Prox1 shows that the PE of avian embryos delivers hemangioblasts but not lymphangioblasts. We have never observed quail ECs in lymphatics of the chick host. However, one exception was a large lymphatic trunk at the base of the chick heart, indicating a lympho-venous anastomosis and a 'homing' mechanism of venous ECs into the lymphatic trunk. Cardiac lymphatics grow from the base toward the apex of the heart. In murine embryos, we observed a basal to apical gradient of scattered Lyve-1+/CD31+/CD45+ cells in the subepicardium at embryonic day 12.5, indicating a contribution of immigrating lymphangioblasts to the cardiac lymphatic system. Our studies show that coronary blood and lymph vessels are derived from different sources, but grow in close association with each other.
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