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Updated: Jun 30, 2026

In Vitro Culture of Epicardial Cells From Mouse Embryonic Heart
Published on: April 27, 2016
Development of the proepicardium in Xenopus laevis
Maike Jahr1, Jan Schlueter, Thomas Brand
1Department of Anatomy and Embryology, Georg-August University of Göttingen, Germany.
Insights
The proepicardium (PE) in Xenopus laevis develops asymmetrically, originating only from the right sinus venosus. This finding suggests PE development is right-sided and may be influenced by left-right signaling pathways.
Area of Science:
- Developmental biology
- Embryology
- Comparative anatomy
Background:
- The proepicardium (PE) is a crucial embryonic progenitor cell population.
- It contributes to the epicardium, cardiac interstitium, and coronary vasculature.
- Recent research highlights paired PE anlagen and species-specific left-right differences.
Purpose of the Study:
- To document proepicardium (PE) development in Xenopus laevis.
- To investigate the origin and pattern of PE development in this species.
- To explore the role of left-right signaling in asymmetric PE development.
Main Methods:
- Morphological observation of PE development in Xenopus laevis embryos (stages 37-46).
- In vivo imaging of tissue bridge formation.
- Expression analysis of the PE marker gene Tbx18.
- Left-right lineage tracing experiments.
Main Results:
- The PE forms as a cone-shaped structure on the right sinus venosus at stage 41, with no left-sided counterpart.
- A tissue bridge forms between the PE and the ventricle, facilitating cell transfer.
- Tbx18 expression and lineage tracing confirm a right-sided origin of the PE.
- Xenopus PE development exhibits a bilaterally asymmetric pattern.
Conclusions:
- Proepicardium development in Xenopus laevis is a bilaterally asymmetric process, originating from the right sinus venosus.
- Asymmetric PE development may be regulated by left-right signaling pathways.
- Xenopus serves as a valuable model for studying asymmetric PE development and its genetic control.
Abstract:
The proepicardium (PE) is an embryonic progenitor cell population, which provides the epicardium, the majority of the cardiac interstitium, the coronary vasculature and possibly some cardiomyocytes. Recent studies have documented (1) the presence of bilaterally paired PE anlagen in several vertebrates, and (2) species-specific differences in the fate of the left and right PE anlagen. Here, we document PE development in Xenopus laevis (stages 37-46). The PE appears at stage 41 in the form of a cone-shaped accumulation of mesothelial cells covering the pericardial surface of the right horn of the sinus venosus. No such structure appears on the left sinus horn. At the end of stage 41, the tip of the PE establishes a firm contact with the developing ventricle. A secondary tissue bridge is established facilitating the transfer of PE cells to the heart. During stages 41-46, this tissue bridge is visible in vivo through the transparent body wall. Corresponding to the morphological data, the PE marker gene Tbx18 is expressed only on the right sinus horn suggesting a right-sided origin of the PE. Left-right lineage tracing has confirmed this idea. These results show that Xenopus PE development proceeds in a bilaterally asymmetric pattern as previously observed in chicks. We speculate that asymmetric PE development is controlled by signals from left-right signaling pathways and that the PE is an indicator for right-sidedness in Xenopus embryos. Xenopus might be a good model to uncover the role of left-right signaling pathways in the control of asymmetric PE development.
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