Evidence map›Paper›PMID 37774033›Full record

ArticleScience advances2023

Epigenetic dynamics during capacitation of naïve human pluripotent stem cells.

João Agostinho de Sousa, Chee-Wai Wong, Ilona Dunkel, Thomas Owens, Philipp Voigt, Adam Hodgson, Duncan Baker, Edda G Schulz, Wolf Reik, Austin Smith and 2 more

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.9field-weighted citation impact, top 9% of its field
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

16 citing papers in PubMed, 19 citations in OpenAlex.

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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

12 authors at 7 institutions in 3 countries.

João Agostinho de SousaLaboratory of Nutrition and Metabolic Epigenetics, Department of Health Sciences and Technology, ETH Zurich, 8603 Schwerzenbach, Switzerland.ORCID 0000-0001-8124-6624
Chee-Wai WongLaboratory of Nutrition and Metabolic Epigenetics, Department of Health Sciences and Technology, ETH Zurich, 8603 Schwerzenbach, Switzerland.ORCID 0000-0002-3972-700X
Ilona DunkelSystems Epigenetics, Otto Warburg Laboratories, Max Planck Institute for Molecular Genetics, 14195 Berlin, Germany.
Thomas OwensEpigenetics Programme, The Babraham Institute, Cambridge CB22 3AT, UK.ORCID 0009-0007-3053-8927
Philipp VoigtEpigenetics Programme, The Babraham Institute, Cambridge CB22 3AT, UK.ORCID 0000-0003-4366-0490
Adam HodgsonSchool of Biosciences, The Julia Garnham Centre, University of Sheffield, S10 2TN Sheffield, UK.ORCID 0000-0002-6933-5752
Duncan BakerSheffield Diagnostic Genetics Services, Sheffield Children's NHS Foundation Trust, S5 7AU Sheffield, UK.ORCID 0000-0002-6475-8246
Edda G SchulzSystems Epigenetics, Otto Warburg Laboratories, Max Planck Institute for Molecular Genetics, 14195 Berlin, Germany.ORCID 0000-0003-1253-6868
Wolf ReikEpigenetics Programme, The Babraham Institute, Cambridge CB22 3AT, UK.ORCID 0000-0003-0216-9881
Austin SmithCambridge Stem Cell Institute, University of Cambridge, Cambridge CB2 0AW, UK.ORCID 0000-0002-3029-4682
Maria RostovskayaEpigenetics Programme, The Babraham Institute, Cambridge CB22 3AT, UK.ORCID 0000-0003-1187-8663
Ferdinand von MeyennLaboratory of Nutrition and Metabolic Epigenetics, Department of Health Sciences and Technology, ETH Zurich, 8603 Schwerzenbach, Switzerland.ORCID 0000-0001-9920-3075
Babraham Institute · GBETH Zurich · CHMax Planck Institute for Molecular Genetics · DEGuy's Hospital · GBSheffield Children's NHS Foundation Trust · GBUniversity of Sheffield · GBWellcome/MRC Cambridge Stem Cell Institute · GB

Funding

Medical Research Council MR/R015724/1Medical Research Council MR/S005536/1Medical Research Council MR/T011769/1Medical Research Council MR/V02969X/1Wellcome Trust 210754/Z/18/Z
6 · The paper itself

Abstract

Human pluripotent stem cells (hPSCs) are of fundamental relevance in regenerative medicine. Naïve hPSCs hold promise to overcome some of the limitations of conventional (primed) hPSCs, including recurrent epigenetic anomalies. Naïve-to-primed transition (capacitation) follows transcriptional dynamics of human embryonic epiblast and is necessary for somatic differentiation from naïve hPSCs. We found that capacitated hPSCs are transcriptionally closer to postimplantation epiblast than conventional hPSCs. This prompted us to comprehensively study epigenetic and related transcriptional changes during capacitation. Our results show that CpG islands, gene regulatory elements, and retrotransposons are hotspots of epigenetic dynamics during capacitation and indicate possible distinct roles of specific epigenetic modifications in gene expression control between naïve and primed hPSCs. Unexpectedly, PRC2 activity appeared to be dispensable for the capacitation. We find that capacitated hPSCs acquire an epigenetic state similar to conventional hPSCs. Significantly, however, the X chromosome erosion frequently observed in conventional female hPSCs is reversed by resetting and subsequent capacitation.

Indexed as

Pluripotent Stem CellsCell DifferentiationEmbryo, MammalianEpigenesis, GeneticFemaleHumans

Identifiers

PMID37774033
PMCPMC10541016
OpenAlexW4387164307

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.