Cargando…
Initial morphological symmetry breaking in the foregut and development of the omental bursa in human embryos
Bilaterally symmetrical primordia of visceral organs undergo asymmetrical morphogenesis leading to typical arrangement of visceral organs in the adult. Asymmetrical morphogenesis within the upper abdomen leads, among others, to the formation of the omental bursa dorsally to the rotated stomach. A wi...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7930768/ https://www.ncbi.nlm.nih.gov/pubmed/33145764 http://dx.doi.org/10.1111/joa.13344 |
_version_ | 1783660154623885312 |
---|---|
author | Schäfer, Tobias Stankova, Viktoria Viebahn, Christoph de Bakker, Bernadette Tsikolia, Nikoloz |
author_facet | Schäfer, Tobias Stankova, Viktoria Viebahn, Christoph de Bakker, Bernadette Tsikolia, Nikoloz |
author_sort | Schäfer, Tobias |
collection | PubMed |
description | Bilaterally symmetrical primordia of visceral organs undergo asymmetrical morphogenesis leading to typical arrangement of visceral organs in the adult. Asymmetrical morphogenesis within the upper abdomen leads, among others, to the formation of the omental bursa dorsally to the rotated stomach. A widespread view of this process assumes kinking of thin mesenteries as a main mechanism. This view is based on a theory proposed already by Johannes Müller in 1830 and was repeatedly criticized, but some of the most plausible alternative views (initially proposed by Swaen in 1897 and Broman in 1904) still remain to be proven. Here, we analyzed serial histological sections of human embryos between stages 12 and 15 at high light microscopical resolution to reveal the succession of events giving rise to the development of the omental bursa and its relation to the emerging stomach asymmetry. Our analysis indicates that morphological symmetry breaking in the upper abdomen occurs within a wide mesenchymal plate called here mesenteric septum and is based on differential behavior of the coelomic epithelium which causes asymmetric paragastric recess formation and, importantly, precedes initial rotation of stomach. Our results thus provide the first histological evidence of breaking the symmetry of the early foregut anlage in the human embryo and pave the way for experimental studies of left‐right symmetry breaking in the upper abdomen in experimental model organisms. |
format | Online Article Text |
id | pubmed-7930768 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79307682021-03-15 Initial morphological symmetry breaking in the foregut and development of the omental bursa in human embryos Schäfer, Tobias Stankova, Viktoria Viebahn, Christoph de Bakker, Bernadette Tsikolia, Nikoloz J Anat Original Papers Bilaterally symmetrical primordia of visceral organs undergo asymmetrical morphogenesis leading to typical arrangement of visceral organs in the adult. Asymmetrical morphogenesis within the upper abdomen leads, among others, to the formation of the omental bursa dorsally to the rotated stomach. A widespread view of this process assumes kinking of thin mesenteries as a main mechanism. This view is based on a theory proposed already by Johannes Müller in 1830 and was repeatedly criticized, but some of the most plausible alternative views (initially proposed by Swaen in 1897 and Broman in 1904) still remain to be proven. Here, we analyzed serial histological sections of human embryos between stages 12 and 15 at high light microscopical resolution to reveal the succession of events giving rise to the development of the omental bursa and its relation to the emerging stomach asymmetry. Our analysis indicates that morphological symmetry breaking in the upper abdomen occurs within a wide mesenchymal plate called here mesenteric septum and is based on differential behavior of the coelomic epithelium which causes asymmetric paragastric recess formation and, importantly, precedes initial rotation of stomach. Our results thus provide the first histological evidence of breaking the symmetry of the early foregut anlage in the human embryo and pave the way for experimental studies of left‐right symmetry breaking in the upper abdomen in experimental model organisms. John Wiley and Sons Inc. 2020-11-03 2021-04 /pmc/articles/PMC7930768/ /pubmed/33145764 http://dx.doi.org/10.1111/joa.13344 Text en © 2020 The Authors. Journal of Anatomy published by John Wiley & Sons Ltd on behalf of Anatomical Society This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Papers Schäfer, Tobias Stankova, Viktoria Viebahn, Christoph de Bakker, Bernadette Tsikolia, Nikoloz Initial morphological symmetry breaking in the foregut and development of the omental bursa in human embryos |
title | Initial morphological symmetry breaking in the foregut and development of the omental bursa in human embryos |
title_full | Initial morphological symmetry breaking in the foregut and development of the omental bursa in human embryos |
title_fullStr | Initial morphological symmetry breaking in the foregut and development of the omental bursa in human embryos |
title_full_unstemmed | Initial morphological symmetry breaking in the foregut and development of the omental bursa in human embryos |
title_short | Initial morphological symmetry breaking in the foregut and development of the omental bursa in human embryos |
title_sort | initial morphological symmetry breaking in the foregut and development of the omental bursa in human embryos |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7930768/ https://www.ncbi.nlm.nih.gov/pubmed/33145764 http://dx.doi.org/10.1111/joa.13344 |
work_keys_str_mv | AT schafertobias initialmorphologicalsymmetrybreakingintheforegutanddevelopmentoftheomentalbursainhumanembryos AT stankovaviktoria initialmorphologicalsymmetrybreakingintheforegutanddevelopmentoftheomentalbursainhumanembryos AT viebahnchristoph initialmorphologicalsymmetrybreakingintheforegutanddevelopmentoftheomentalbursainhumanembryos AT debakkerbernadette initialmorphologicalsymmetrybreakingintheforegutanddevelopmentoftheomentalbursainhumanembryos AT tsikolianikoloz initialmorphologicalsymmetrybreakingintheforegutanddevelopmentoftheomentalbursainhumanembryos |