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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2022
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.
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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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