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Deciphering epiblast lumenogenesis reveals proamniotic cavity control of embryo growth and patterning
During the peri-implantation stages, the mouse embryo radically changes its appearance, transforming from a hollow-shaped blastocyst to an egg cylinder. At the same time, the epiblast gets reorganized from a simple ball of cells to a cup-shaped epithelial monolayer enclosing the proamniotic cavity....
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7946377/ https://www.ncbi.nlm.nih.gov/pubmed/33692105 http://dx.doi.org/10.1126/sciadv.abe1640 |
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author | Kim, Yung Su Fan, Rui Kremer, Ludmila Kuempel-Rink, Nannette Mildner, Karina Zeuschner, Dagmar Hekking, Liesbeth Stehling, Martin Bedzhov, Ivan |
author_facet | Kim, Yung Su Fan, Rui Kremer, Ludmila Kuempel-Rink, Nannette Mildner, Karina Zeuschner, Dagmar Hekking, Liesbeth Stehling, Martin Bedzhov, Ivan |
author_sort | Kim, Yung Su |
collection | PubMed |
description | During the peri-implantation stages, the mouse embryo radically changes its appearance, transforming from a hollow-shaped blastocyst to an egg cylinder. At the same time, the epiblast gets reorganized from a simple ball of cells to a cup-shaped epithelial monolayer enclosing the proamniotic cavity. However, the cavity’s function and mechanism of formation have so far been obscure. Through investigating the cavity formation, we found that in the epiblast, the process of lumenogenesis is driven by reorganization of intercellular adhesion, vectoral fluid transport, and mitotic paracellular water influx from the blastocoel into the emerging proamniotic cavity. By experimentally blocking lumenogenesis, we found that the proamniotic cavity functions as a hub for communication between the early lineages, enabling proper growth and patterning of the postimplantation embryo. |
format | Online Article Text |
id | pubmed-7946377 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-79463772021-03-23 Deciphering epiblast lumenogenesis reveals proamniotic cavity control of embryo growth and patterning Kim, Yung Su Fan, Rui Kremer, Ludmila Kuempel-Rink, Nannette Mildner, Karina Zeuschner, Dagmar Hekking, Liesbeth Stehling, Martin Bedzhov, Ivan Sci Adv Research Articles During the peri-implantation stages, the mouse embryo radically changes its appearance, transforming from a hollow-shaped blastocyst to an egg cylinder. At the same time, the epiblast gets reorganized from a simple ball of cells to a cup-shaped epithelial monolayer enclosing the proamniotic cavity. However, the cavity’s function and mechanism of formation have so far been obscure. Through investigating the cavity formation, we found that in the epiblast, the process of lumenogenesis is driven by reorganization of intercellular adhesion, vectoral fluid transport, and mitotic paracellular water influx from the blastocoel into the emerging proamniotic cavity. By experimentally blocking lumenogenesis, we found that the proamniotic cavity functions as a hub for communication between the early lineages, enabling proper growth and patterning of the postimplantation embryo. American Association for the Advancement of Science 2021-03-10 /pmc/articles/PMC7946377/ /pubmed/33692105 http://dx.doi.org/10.1126/sciadv.abe1640 Text en Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Kim, Yung Su Fan, Rui Kremer, Ludmila Kuempel-Rink, Nannette Mildner, Karina Zeuschner, Dagmar Hekking, Liesbeth Stehling, Martin Bedzhov, Ivan Deciphering epiblast lumenogenesis reveals proamniotic cavity control of embryo growth and patterning |
title | Deciphering epiblast lumenogenesis reveals proamniotic cavity control of embryo growth and patterning |
title_full | Deciphering epiblast lumenogenesis reveals proamniotic cavity control of embryo growth and patterning |
title_fullStr | Deciphering epiblast lumenogenesis reveals proamniotic cavity control of embryo growth and patterning |
title_full_unstemmed | Deciphering epiblast lumenogenesis reveals proamniotic cavity control of embryo growth and patterning |
title_short | Deciphering epiblast lumenogenesis reveals proamniotic cavity control of embryo growth and patterning |
title_sort | deciphering epiblast lumenogenesis reveals proamniotic cavity control of embryo growth and patterning |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7946377/ https://www.ncbi.nlm.nih.gov/pubmed/33692105 http://dx.doi.org/10.1126/sciadv.abe1640 |
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