The DOI matches its Crossref record; 47 of the 47 references it cites were found in a registry or an index.
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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Embryonic Stem Cell Lines Derived from Human Blastocysts
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Human DNA methylomes at base resolution show widespread epigenomic differences
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New cell lines from mouse epiblast share defining features with human embryonic stem cells
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Self-citationDerivation of pluripotent epiblast stem cells from mammalian embryos
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The SRA protein Np95 mediates epigenetic inheritance by recruiting Dnmt1 to methylated DNA
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Derivation of Human Trophoblast Stem Cells
Okae, H., Toh, H., Sato, T., Hiura, H., Takahashi, S., Shirane, K., Kabayama, Y., Suyama, M., Sasaki, H., & Arima, T. (2017) · Cell stem cell · doi:10.1016/j.stem.2017.11.004 · Cited by 915
Human placenta and trophoblast development: key molecular mechanisms and model systems
Knöfler, M., Haider, S., Saleh, L., Pollheimer, J., Gamage, T. K. J. B., & James, J. L. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03104-6 · Cited by 818
Placental Origins of Chronic Disease
Burton, G. J., Fowden, A. L., & Thornburg, K. L. (2016) · Physiological Reviews · doi:10.1152/physrev.00029.2015 · Cited by 717
Self-citationDevelopment of the human placenta
Turco, M. Y., & Moffett, A. (2019) · Development · doi:10.1242/dev.163428 · Cited by 742
Trophoblast organoids as a model for maternal–fetal interactions during human placentation
Turco, M. Y., Gardner, L., Kay, R. G., Hamilton, R. S., Prater, M., Hollinshead, M. S., McWhinnie, A., Esposito, L., Fernando, R. C., Skelton, H. E., et al. (2018) · Nature · doi:10.1038/s41586-018-0753-3 · Cited by 717
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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
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