An in vitro stem cell model of human epiblast and yolk sac interaction

Author:

Mackinlay Kirsty ML1ORCID,Weatherbee Bailey AT1ORCID,Souza Rosa Viviane123,Handford Charlotte E14,Hudson George1ORCID,Coorens Tim5,Pereira Lygia V2,Behjati Sam5,Vallier Ludovic6ORCID,Shahbazi Marta N13ORCID,Zernicka-Goetz Magdalena17ORCID

Affiliation:

1. Mammalian Embryo and Stem Cell Group, University of Cambridge, Department of Physiology, Development and Neuroscience, Cambridge, United Kingdom

2. National Laboratory for Embryonic Stem Cells (LaNCE), Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of São Paulo, São Paulo, Brazil

3. MRC Laboratory of Molecular Biology, Cambridge Biomedical Campus, Cambridge, United Kingdom

4. Centre for Trophoblast Research, University of Cambridge, Cambridge, United Kingdom

5. Wellcome Sanger Institute, Cambridge, United Kingdom

6. Wellcome – MRC Cambridge Stem Cell Institute, Cambridge Biomedical Campus, Cambridge, United Kingdom

7. Synthetic Mouse and Human Embryology Group, California Institute of Technology (Caltech), Division of Biology and Biological Engineering, Pasadena, United States

Abstract

Human embryogenesis entails complex signalling interactions between embryonic and extra-embryonic cells. However, how extra-embryonic cells direct morphogenesis within the human embryo remains largely unknown due to a lack of relevant stem cell models. Here, we have established conditions to differentiate human pluripotent stem cells (hPSCs) into yolk sac-like cells (YSLCs) that resemble the post-implantation human hypoblast molecularly and functionally. YSLCs induce the expression of pluripotency and anterior ectoderm markers in human embryonic stem cells (hESCs) at the expense of mesoderm and endoderm markers. This activity is mediated by the release of BMP and WNT signalling pathway inhibitors, and, therefore, resembles the functioning of the anterior visceral endoderm signalling centre of the mouse embryo, which establishes the anterior-posterior axis. Our results implicate the yolk sac in epiblast cell fate specification in the human embryo and propose YSLCs as a tool for studying post-implantation human embryo development in vitro.

Funder

Biotechnology and Biological Sciences Research Council

Medical Research Council

European Molecular Biology Laboratory

Wellcome Trust

National Institutes of Health

European Research Council

University of Cambridge

Gates Cambridge Trust

European Molecular Biology Organization

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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