4.8 Article

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

Journal

ELIFE
Volume 10, Issue -, Pages -

Publisher

eLIFE SCIENCES PUBL LTD
DOI: 10.7554/eLife.63930

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Funding

  1. Biotechnology and Biological Sciences Research Council [1943755]
  2. Medical Research Council [MC_UP_1201/24]
  3. European Molecular Biology Laboratory
  4. Wellcome Trust [207415/Z/17/Z]
  5. National Institutes of Health [HD100456-01A1, DP1 HD104575-01]
  6. European Research Council [669198]
  7. University of Cambridge
  8. Gates Cambridge Trust
  9. European Molecular Biology Organization
  10. BBSRC [1943755] Funding Source: UKRI
  11. MRC [MC_UP_1201/24] Funding Source: UKRI

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This study established conditions to differentiate human pluripotent stem cells into yolk sac-like cells and found that these cells can induce the expression of specific markers in human embryonic stem cells. The results suggest a crucial role of the yolk sac in epiblast cell fate specification in the human embryo.
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.

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