Evidence map›Paper›PMID 32048992›Full record

ArticleeLife2020

Derivation of trophoblast stem cells from naïve human pluripotent stem cells.

Chen Dong, Mariana Beltcheva, Paul Gontarz, Bo Zhang, Pooja Popli, Laura A Fischer, Shafqat A Khan, Kyoung-Mi Park, Eun-Ja Yoon, Xiaoyun Xing and 4 more

Abstract read
In one paragraph

Article in eLife, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 191 papers.

0numbers the graph read from it
0cells of the map it votes in
191citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

191 citing papers in PubMed.

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  15. Review
  16. Article
  17. Mechanisms of human germ cell development.Nature reviews. Molecular cell biology · 2026
    Review
  18. Article
  19. Review
  20. Modeling Aspects of Human Placental Development with Trophoblast Stem Cells.Methods in molecular biology (Clifton, N.J.) · 2026
    Article

131 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Chen DongDepartment of Developmental Biology, Washington University School of Medicine, St. Louis, United States.ORCID 0000-0002-5405-5715
Mariana BeltchevaDepartment of Developmental Biology, Washington University School of Medicine, St. Louis, United States.
Paul GontarzDepartment of Developmental Biology, Washington University School of Medicine, St. Louis, United States.
Bo ZhangDepartment of Developmental Biology, Washington University School of Medicine, St. Louis, United States.
Pooja PopliDepartment of Obstetrics and Gynecology, Center for Reproductive Health Sciences, Washington University School of Medicine, St. Louis, United States.
Laura A FischerDepartment of Developmental Biology, Washington University School of Medicine, St. Louis, United States.
Shafqat A KhanDepartment of Developmental Biology, Washington University School of Medicine, St. Louis, United States.
Kyoung-Mi ParkDepartment of Developmental Biology, Washington University School of Medicine, St. Louis, United States.
Eun-Ja YoonDepartment of Developmental Biology, Washington University School of Medicine, St. Louis, United States.
Xiaoyun XingCenter of Regenerative Medicine, Washington University School of Medicine, St. Louis, United States.
Ramakrishna KommaganiDepartment of Obstetrics and Gynecology, Center for Reproductive Health Sciences, Washington University School of Medicine, St. Louis, United States.ORCID 0000-0003-0403-0971
Ting WangCenter of Regenerative Medicine, Washington University School of Medicine, St. Louis, United States.
Lilianna Solnica-KrezelDepartment of Developmental Biology, Washington University School of Medicine, St. Louis, United States.
Thorold W TheunissenDepartment of Developmental Biology, Washington University School of Medicine, St. Louis, United States.ORCID 0000-0001-6943-7858

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI TIMOTHY J. EBERLEIN · 2001 to 2026
$128.0M
WU INSTITUTE OF CLINICAL AND TRANSLATIONAL SCIENCESUL1TR002345 · NCATS · WASHINGTON UNIVERSITY · PI William G. Powderly · 2017 to 2026
$97.8M
Washington University Institute of Clinical and Translational SciencesUL1TR000448 · NCATS · WASHINGTON UNIVERSITY · PI EVANOFF, BRADLEY A · 2012 to 2016
$41.4M
The WashU-UCSC-EBI Human Genome Reference Center."U41HG010972 · NHGRI · WASHINGTON UNIVERSITY · PI Ira M Hall, Heng Li · 2019 to 2026
$24.9M
THE WASHU TARGET ENVIRONMENTAL EPIGENOMICS DATA COORDINATION CENTERU24ES026699 · NIEHS · WASHINGTON UNIVERSITY · PI WANG, TING · 2016 to 2021
$5.2M
MOLECULAR AND METABOLIC ASPECTS OF IMPLANTATIONR01HD065435 · NICHD · WASHINGTON UNIVERSITY · PI KOMMAGANI, RAMAKRISHNA, SANTI, CELIA M · 2010 to 2020
$4.5M
SLO3 KO MOUSE: A TOOL TO REVEAL VOLTAGE-DEPENDENT PROCESSES IN SPERM FERTILITYR01HD069631 · NICHD · WASHINGTON UNIVERSITY · PI SANTI, CELIA M · 2011 to 2022
$3.3M
DECODING THE IMPACT OF TRANSPOSABLE ELEMENTS ON GENE REGULATIONR01HG007175 · NHGRI · WASHINGTON UNIVERSITY · PI WANG, TING · 2014 to 2021
$2.7M
Resolving epigenetic instability during pluripotent state transitions: a roadmap for exploiting the biomedical potential of dynamic human stem cell statesDP2GM137418 · NIGMS · WASHINGTON UNIVERSITY · PI THEUNISSEN, THOROLD · 2019 to 2019
$2.4M
The WashU 4DN Network Data Coordination and Integration CenterU01CA200060 · NCI · WASHINGTON UNIVERSITY · PI WANG, TING · 2015 to 2019
$1.9M
GREB1 Action in Endometrial Function and DysfunctionR00HD080742 · NICHD · WASHINGTON UNIVERSITY · PI KOMMAGANI, RAMAKRISHNA · 2017 to 2019
$702k
NCATS NIH HHS UL1 TR000448NCATS NIH HHS UL1 TR002345NCI NIH HHS P30 CA091842NCI NIH HHS U01 CA200060NHGRI NIH HHS R01 HG007175NHGRI NIH HHS U41 HG010972NICHD NIH HHS R00 HD080742NICHD NIH HHS R01 HD065435NICHD NIH HHS R01 HD069631NIEHS NIH HHS U24 ES026699NIGMS NIH HHS DP2 GM137418
6 · The paper itself

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.

Indexed as

Cell DifferentiationBiomarkersCell LineageCulture MediaEmbryoid BodiesHumansPluripotent Stem CellsStem CellsTrophoblastsBiomarkersCulture MediaATAC-seqhumannaive pluripotencyprimed pluripotencyregenerative medicineRNA-seqstem cellstrophectodermtrophoblast stem cells

Identifiers

PMID32048992
PMCPMC7062471

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.