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A pendulum of induction between the epiblast and extra-embryonic endoderm supports post-implantation progression
Embryogenesis is supported by dynamic loops of cellular interactions. Here, we create a partial mouse embryo model to elucidate the principles of epiblast (Epi) and extra-embryonic endoderm co-development (XEn). We trigger naive mouse embryonic stem cells to form a blastocyst-stage niche of Epi-like...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9534490/ https://www.ncbi.nlm.nih.gov/pubmed/35993866 http://dx.doi.org/10.1242/dev.192310 |
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author | Vrij, Erik J. Scholte op Reimer, Yvonne S. Fuentes, Laury Roa Guerreiro, Isabel Misteli Holzmann, Viktoria Aldeguer, Javier Frias Sestini, Giovanni Koo, Bon-Kyoung Kind, Jop van Blitterswijk, Clemens A. Rivron, Nicolas C. |
author_facet | Vrij, Erik J. Scholte op Reimer, Yvonne S. Fuentes, Laury Roa Guerreiro, Isabel Misteli Holzmann, Viktoria Aldeguer, Javier Frias Sestini, Giovanni Koo, Bon-Kyoung Kind, Jop van Blitterswijk, Clemens A. Rivron, Nicolas C. |
author_sort | Vrij, Erik J. |
collection | PubMed |
description | Embryogenesis is supported by dynamic loops of cellular interactions. Here, we create a partial mouse embryo model to elucidate the principles of epiblast (Epi) and extra-embryonic endoderm co-development (XEn). We trigger naive mouse embryonic stem cells to form a blastocyst-stage niche of Epi-like cells and XEn-like cells (3D, hydrogel free and serum free). Once established, these two lineages autonomously progress in minimal medium to form an inner pro-amniotic-like cavity surrounded by polarized Epi-like cells covered with visceral endoderm (VE)-like cells. The progression occurs through reciprocal inductions by which the Epi supports the primitive endoderm (PrE) to produce a basal lamina that subsequently regulates Epi polarization and/or cavitation, which, in return, channels the transcriptomic progression to VE. This VE then contributes to Epi bifurcation into anterior- and posterior-like states. Similarly, boosting the formation of PrE-like cells within blastoids supports developmental progression. We argue that self-organization can arise from lineage bifurcation followed by a pendulum of induction that propagates over time. |
format | Online Article Text |
id | pubmed-9534490 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-95344902022-10-25 A pendulum of induction between the epiblast and extra-embryonic endoderm supports post-implantation progression Vrij, Erik J. Scholte op Reimer, Yvonne S. Fuentes, Laury Roa Guerreiro, Isabel Misteli Holzmann, Viktoria Aldeguer, Javier Frias Sestini, Giovanni Koo, Bon-Kyoung Kind, Jop van Blitterswijk, Clemens A. Rivron, Nicolas C. Development Stem Cells and Regeneration Embryogenesis is supported by dynamic loops of cellular interactions. Here, we create a partial mouse embryo model to elucidate the principles of epiblast (Epi) and extra-embryonic endoderm co-development (XEn). We trigger naive mouse embryonic stem cells to form a blastocyst-stage niche of Epi-like cells and XEn-like cells (3D, hydrogel free and serum free). Once established, these two lineages autonomously progress in minimal medium to form an inner pro-amniotic-like cavity surrounded by polarized Epi-like cells covered with visceral endoderm (VE)-like cells. The progression occurs through reciprocal inductions by which the Epi supports the primitive endoderm (PrE) to produce a basal lamina that subsequently regulates Epi polarization and/or cavitation, which, in return, channels the transcriptomic progression to VE. This VE then contributes to Epi bifurcation into anterior- and posterior-like states. Similarly, boosting the formation of PrE-like cells within blastoids supports developmental progression. We argue that self-organization can arise from lineage bifurcation followed by a pendulum of induction that propagates over time. The Company of Biologists Ltd 2022-08-22 /pmc/articles/PMC9534490/ /pubmed/35993866 http://dx.doi.org/10.1242/dev.192310 Text en © 2022. Published by The Company of Biologists Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Stem Cells and Regeneration Vrij, Erik J. Scholte op Reimer, Yvonne S. Fuentes, Laury Roa Guerreiro, Isabel Misteli Holzmann, Viktoria Aldeguer, Javier Frias Sestini, Giovanni Koo, Bon-Kyoung Kind, Jop van Blitterswijk, Clemens A. Rivron, Nicolas C. A pendulum of induction between the epiblast and extra-embryonic endoderm supports post-implantation progression |
title | A pendulum of induction between the epiblast and extra-embryonic endoderm supports post-implantation progression |
title_full | A pendulum of induction between the epiblast and extra-embryonic endoderm supports post-implantation progression |
title_fullStr | A pendulum of induction between the epiblast and extra-embryonic endoderm supports post-implantation progression |
title_full_unstemmed | A pendulum of induction between the epiblast and extra-embryonic endoderm supports post-implantation progression |
title_short | A pendulum of induction between the epiblast and extra-embryonic endoderm supports post-implantation progression |
title_sort | pendulum of induction between the epiblast and extra-embryonic endoderm supports post-implantation progression |
topic | Stem Cells and Regeneration |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9534490/ https://www.ncbi.nlm.nih.gov/pubmed/35993866 http://dx.doi.org/10.1242/dev.192310 |
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