A pendulum of induction between the epiblast and extra-embryonic endoderm supports post-implantation progression

Author:

Vrij Erik J.12,Scholte op Reimer Yvonne S.2,Fuentes Laury Roa1,Guerreiro Isabel Misteli3,Holzmann Viktoria2,Aldeguer Javier Frias13,Sestini Giovanni2,Koo Bon-Kyoung2,Kind Jop34,van Blitterswijk Clemens A.1,Rivron Nicolas C.2ORCID

Affiliation:

1. MERLN Institute for Technology-inspired Regenerative Medicine, Maastricht University 1 , Universiteitssingel 40, 6229 ER Maastricht , Netherlands

2. Institute of Molecular Biotechnology of the Austrian Academy of Sciences 2 , Vienna Biocenter, Dr. Bohr-Gasse 3, 1030 Vienna , Austria

3. Hubrecht Institute, Royal Netherlands Academy of Arts and Sciences (KNAW) and University Medical Center Utrecht 3 , UtrechtUppsalalaan 8, 3584 CT Utrecht , Netherlands

4. Department of Molecular Biology, Faculty of Science 4 , Radboud Institute for Molecular Life Sciences, Radboud University Nijmegen, Geert Grooteplein Zuid 10, 6525 GA Nijmegen , Netherlands

Abstract

ABSTRACT 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.

Funder

European Research Council

Stichting De Weijerhorst

Boehringer Ingelheim Fonds

European Molecular Biology Organization

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Nederlandse Organisatie voor Wetenschappelijk Onderzoek

Österreichischen Akademie der Wissenschaften

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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