Transcription factor-based transdifferentiation of human embryonic to trophoblast stem cells

During the first week of development, human embryos form a blastocyst composed of an inner cell mass and trophectoderm (TE) cells, the latter of which are progenitors of placental trophoblast. Here, we investigated the expression of transcripts in the human TE from early to late blastocyst stages. We identified enrichment of the transcription factors GATA2, GATA3, TFAP2C and KLF5 and characterised their protein expression dynamics across TE development. By inducible overexpression and mRNA transfection, we determined that these factors, together with MYC, are sufficient to establish induced trophoblast stem cells (iTSCs) from primed human embryonic stem cells. These iTSCs self-renew and recapitulate morphological characteristics, gene expression profiles, and directed differentiation potential, similar to existing human TSCs. Systematic omission of each, or combinations of factors, revealed the crucial importance of GATA2 and GATA3 for iTSC transdifferentiation. Altogether, these findings provide insights into the transcription factor network that may be operational in the human TE and broaden the methods for establishing cellular models of early human placental progenitor cells, which may be useful in the future to model placental-associated diseases.

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Publication Details

Journal
Development
Published
2024-09-01
DOI
https://doi.org/10.1242/dev.202778
Citations
5
Primary Topic
Pluripotent Stem Cells Research
Type
article
Field-Weighted Citation Impact
1.17

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article

Transcription factor-based transdifferentiation of human embryonic to trophoblast stem cells

Claire E. Senner, Rabi Odia, Leila Christie, Alice E. Chen et al.
5 citations
Development
Pluripotent Stem Cells Research
1.17
article

Transcription factor-based transdifferentiation of human embryonic to trophoblast stem cells

Claire E. Senner, Rabi Odia, Leila Christie, Alice E. Chen, Kay Elder, Ahmed Abdelbaki, Prabhakaran Munusamy, Paul Blakeley, Liani Devito, Mahesh Sangrithi, Phil Snell, Afshan McCarthy, Kathy K. Niakan, Paula A. Balestrini, Norah M. E. Fogarty, Paul Serhal
article en
5 citations

Abstract

During the first week of development, human embryos form a blastocyst composed of an inner cell mass and trophectoderm (TE) cells, the latter of which are progenitors of placental trophoblast. Here, we investigated the expression of transcripts in the human TE from early to late blastocyst stages. We identified enrichment of the transcription factors GATA2, GATA3, TFAP2C and KLF5 and characterised their protein expression dynamics across TE development. By inducible overexpression and mRNA transfection, we determined that these factors, together with MYC, are sufficient to establish induced trophoblast stem cells (iTSCs) from primed human embryonic stem cells. These iTSCs self-renew and recapitulate morphological characteristics, gene expression profiles, and directed differentiation potential, similar to existing human TSCs. Systematic omission of each, or combinations of factors, revealed the crucial importance of GATA2 and GATA3 for iTSC transdifferentiation. Altogether, these findings provide insights into the transcription factor network that may be operational in the human TE and broaden the methods for establishing cellular models of early human placental progenitor cells, which may be useful in the future to model placental-associated diseases.

DevelopmentVol. 151(17)
Babraham Institute (GB), Chinese University of Hong Kong (HK), King's College London (GB), Zagazig University (EG), Bourn Hall Clinic (GB), University of Cambridge (GB), The Francis Crick Institute (GB), Cell and Gene Therapy Catapult (GB), KK Women's and Children's Hospital (SG), MRC Centre for Reproductive Health (GB), Duke-NUS Medical School (SG), Stem Cell Institute (PA), The Centre for Reproductive & Genetic Health, Wellcome Trust (GB), University of Hong Kong (HK), Medical Research Council (GB)
Wellcome Trust, Francis Crick Institute, UK Research and Innovation, National Medical Research Council
Openalex Percentile: Top 22%
Pluripotent Stem Cells Research
1.17
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