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Published on: December 16, 2022
Morphological and molecular left-right asymmetries in the development of the proepicardium: a comparative analysis on
Inga Schulte1, Jan Schlueter, Radwan Abu-Issa
1Department of Anatomy and Embryology, Georg-August University of Göttingen, Germany.
Insights
The proepicardium (PE) develops bilaterally in mice but asymmetrically in chicks, with only the right side forming fully. This suggests the left-right pathway influences chick PE development, unlike in mice.
Area of Science:
- Developmental biology
- Embryology
- Comparative embryology
Background:
- The proepicardium (PE) is a crucial embryonic progenitor cell population.
- PE contributes to the epicardium, cardiac interstitium, and coronary vasculature.
- Understanding PE development is key to cardiac formation.
Purpose of the Study:
- To compare proepicardium (PE) development in mouse and chick embryos.
- To investigate the mechanisms underlying asymmetric PE development in chick embryos.
- To determine the role of the left-right (L-R) pathway in PE development.
Main Methods:
- Comparative morphological analysis of PE development in mouse and chick embryos.
- Gene expression analysis of PE marker genes (Tbx18, Wt1) and Bmp4.
- Experimental manipulation of chick embryos: induced topographical inversion, organ culture, and cardia bifida induction.
Main Results:
- Mouse PE development is bilateral, with simultaneous left and right anlage merging.
- Chick PE development is unilateral, with the right anlage developing fully and the left remaining rudimentary.
- Experimental manipulations in chick embryos consistently resulted in only the right PE developing the full phenotype.
- Gene expression patterns (Tbx18, Wt1, Bmp4) differed between mouse and chick PE development.
Conclusions:
- Proepicardium (PE) development exhibits species-specific differences between mice and chicks.
- Asymmetric PE development in chicks may be regulated by the left-right (L-R) pathway.
- Mouse PE development does not appear to be controlled by the L-R pathway.
- Topographical relationships and intrinsic factors likely influence PE development.
Abstract:
The proepicardium (PE) is an embryonic progenitor cell population that delivers the epicardium, the majority of the cardiac interstitium, and the coronary vasculature. In the present study, we compared PE development in mouse and chick embryos. In the mouse, a left and a right PE anlage appear simultaneously, which subsequently merge at the embryonic midline to form a single PE. In chick embryos, the right PE anlage appears earlier than the left and only the right anlage acquires the full PE-phenotype. The left anlage remains in a rudimentary state. The expression patterns of PE marker genes (Tbx18, Wt1) correspond to the morphological data, being bilateral in the mouse and unilateral in the chick. Bmp4, which is unilaterally expressed in the right PE of chick embryos, is symmetrically expressed in the sinus venosus wall cranial to the PE in mouse embryos. Asymmetric development of the chicken PE might reflect side-specific differences in topographical relationships to tissues with PE-inducing or repressing activity or might result from the PE-repressing activity of the right PE, which grows earlier. To test these hypotheses, we analyzed PE development in chick embryos, firstly, subsequent to experimentally induced inversion of PE topographical relationships to neighbouring tissues; secondly, in organ cultures; and, thirdly, subsequent to induction of cardia bifida. In all three experiments, only the right PE develops the full PE phenotype. Our results suggest that PE development might be controlled by the L-R pathway in the chick but not in the mouse embryo.
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