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ELF5-enforced transcriptional networks define an epigenetically regulated trophoblast stem cell compartment in the human placenta
Abstract
The first definitive cell fate decision in development occurs at the blastocyst stage with establishment of the trophoblast and embryonic cell lineages. In the mouse, lineage commitment is achieved by epigenetic regulation of a critical gatekeeper gene, the transcription factor Elf5, that reinforces placental cell fate and is necessary for trophoblast stem (TS) cell self-renewal. In humans, however, the epigenetic lineage boundary seems to be less stringent since human embryonic stem (ES) cells, unlike their murine counterparts, harbour some potential to differentiate into trophoblast derivatives. Here, we show that ELF5 is expressed in the human placenta in villous cytotrophoblast cells but not in post-mitotic syncytiotrophoblast and invasive extravillous cytotrophoblast cells. ELF5 establishes a circuit of mutually interacting transcription factors with CDX2 and EOMES, and the highly proliferative ELF5(+)/CDX2(+) double-positive subset of cytotrophoblast cells demarcates a putative TS cell compartment in the early human placenta. In contrast to placental trophoblast, however, ELF5 is hypermethylated and largely repressed in human ES cells and derived trophoblast cell lines, as well as in induced pluripotent stem cells and murine epiblast stem cells. Thus, these cells exhibit an embryonic lineage-specific epigenetic signature and do not undergo an epigenetic reprogramming to reflect the trophoblast lineage at key loci such as ELF5. Our identification of the trophoblast-specific transcriptional circuit established by ELF5 will be instrumental to derive human TS cell lines that truly reflect early placental trophoblast and that will be most beneficial to gain insights into the aetiology of common pregnancy complications, including intra-uterine growth restriction and pre-eclampsia.
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“The first trimester is a critical period for placental development, for expression of markers of trophoblast stemness decline rapidly after 12 weeks of gestation (252), suggesting loss of proliferative potential.”
From Placental Origins of Chronic Disease (2016) · cites this paper as [252]
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Metadata
- Authors
- Hemberger, M., Udayashankar, R., Tesar, P., Moore, H., & Burton, G. J.
- Affiliations
- Babraham Institute (GB)
- University of Sheffield (GB)
- Case Western Reserve University (US)
- University of Cambridge (GB)
- Corresponding author
- Hemberger, Myriam
- Venue
- Human Molecular Genetics
- Publisher
- Oxford University Press (OUP)
- Published
- 2010-03-30
- Volume
- 19
- Issue
- 12
- Pages
- 2456-2467
- ISSN
- 0964-6906 (ISSN-L)
- 1460-2083
- OpenAlex
- W2134873562
- Cited by
- 181
- References
- 47
- Citations by year
- 2026: 3 · 2025: 9 · 2024: 6 · 2023: 6 · 2022: 14 · 2021: 13 · 2020: 10 · 2019: 12 · 2018: 12 · 2017: 11 · 2016: 14 · 2015: 8 · 2014: 9 · 2013: 17 · 2012: 24
- FWCI
- 7.04
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Human Molecular Genetics (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Medical Research Council
- Biotechnology and Biological Sciences Research Council (BBS/E/B/0000C230)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Pluripotent Stem Cells Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Keywords
- ELF5, trophoblast stem cells, human placenta, epigenetic regulation, transcriptional regulatory networks, CDX2, Eomes, cytotrophoblast, syncytiotrophoblast, extravillous cytotrophoblast, DNA methylation, human embryonic stem cells, induced pluripotent stem cells, epiblast stem cells, fetal growth restriction, preeclampsia
- MeSH terms
- CDX2 Transcription Factor, Animals, DNA-Binding Proteins, Female, Humans, Placenta, Pregnancy, Pregnancy Complications, Stem Cells, Transcription Factors, Trophoblasts, Homeodomain Proteins, Cell Lineage, DNA Methylation, Oligonucleotide Array Sequence Analysis, T-Box Domain Proteins, Pluripotent Stem Cells, Epigenesis, Genetic, Proto-Oncogene Proteins c-ets, Mice, Gene Regulatory Networks
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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