Derivation of trophoblast stem cells from naïve human pluripotent stem cells

Author:

Dong Chen12ORCID,Beltcheva Mariana12,Gontarz Paul12,Zhang Bo12,Popli Pooja3,Fischer Laura A12,Khan Shafqat A12,Park Kyoung-mi12,Yoon Eun-Ja12,Xing Xiaoyun24,Kommagani Ramakrishna3ORCID,Wang Ting24,Solnica-Krezel Lilianna12,Theunissen Thorold W12ORCID

Affiliation:

1. Department of Developmental Biology, Washington University School of Medicine, St. Louis, United States

2. Center of Regenerative Medicine, Washington University School of Medicine, St. Louis, United States

3. Department of Obstetrics and Gynecology, Center for Reproductive Health Sciences, Washington University School of Medicine, St. Louis, United States

4. Department of Genetics, Center for Genome Sciences & Systems Biology, Washington University School of Medicine, St. Louis, United States

Abstract

Naïve human pluripotent stem cells (hPSCs) provide a unique experimental platform of cell fate decisions during pre-implantation development, but their lineage potential remains incompletely characterized. As naïve hPSCs share transcriptional and epigenomic signatures with trophoblast cells, it has been proposed that the naïve state may have enhanced predisposition for differentiation along this extraembryonic lineage. Here we examined the trophoblast potential of isogenic naïve and primed hPSCs. We found that naïve hPSCs can directly give rise to human trophoblast stem cells (hTSCs) and undergo further differentiation into both extravillous and syncytiotrophoblast. In contrast, primed hPSCs do not support hTSC derivation, but give rise to non-self-renewing cytotrophoblasts in response to BMP4. Global transcriptome and chromatin accessibility analyses indicate that hTSCs derived from naïve hPSCs are similar to blastocyst-derived hTSCs and acquire features of post-implantation trophectoderm. The derivation of hTSCs from naïve hPSCs will enable elucidation of early mechanisms that govern normal human trophoblast development and associated pathologies.

Funder

Children's Discovery Institute

McDonnell Center for Cellular and Molecular Neurobiology

NIH Office of the Director

Shipley Foundation

Edward Mallinckrodt, Jr. Foundation

Publisher

eLife Sciences Publications, Ltd

Subject

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

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