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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....

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Autores principales: Kim, Yung Su, Fan, Rui, Kremer, Ludmila, Kuempel-Rink, Nannette, Mildner, Karina, Zeuschner, Dagmar, Hekking, Liesbeth, Stehling, Martin, Bedzhov, Ivan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2021
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.
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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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