Evidence map›Paper›PMID 33452132›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2021

OCT4 induces embryonic pluripotency via STAT3 signaling and metabolic mechanisms.

Giuliano G Stirparo, Agata Kurowski, Ayaka Yanagida, Lawrence E Bates, Stanley E Strawbridge, Siarhei Hladkou, Hannah T Stuart, Thorsten E Boroviak, Jose C R Silva, Jennifer Nichols

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
4.4field-weighted citation impact, top 4% 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

29 citing papers in PubMed, 65 citations in OpenAlex.

  1. Article
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  8. Coupling of stemness maintenance with cell cycle control in stem cells.Frontiers in cell and developmental biology · 2025
    Review
  9. Article
  10. Signaling pathway regulators in preimplantation embryos.Journal of molecular histology · 2024
    Review
  11. Article
  12. Article
  13. Article
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  15. Article
  16. The role of lipids in genome integrity and pluripotency.Biochemical Society transactions · 2024
    Review
  17. Article
  18. Article
  19. Article
  20. Review
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

10 authors at 2 institutions in 2 countries.

Giuliano G StirparoWellcome Trust-Medical Research Council Stem Cell Institute, Jeffrey Cheah Biomedical Centre, University of Cambridge, CB2 0AW Cambridge, United Kingdom; jn270@cam.ac.uk ggs28@cam.ac.uk.ORCID 0000-0002-5911-8682
Agata KurowskiWellcome Trust-Medical Research Council Stem Cell Institute, Jeffrey Cheah Biomedical Centre, University of Cambridge, CB2 0AW Cambridge, United Kingdom.ORCID 0000-0003-0502-571X
Ayaka YanagidaWellcome Trust-Medical Research Council Stem Cell Institute, Jeffrey Cheah Biomedical Centre, University of Cambridge, CB2 0AW Cambridge, United Kingdom.ORCID 0000-0002-6350-2185
Lawrence E BatesWellcome Trust-Medical Research Council Stem Cell Institute, Jeffrey Cheah Biomedical Centre, University of Cambridge, CB2 0AW Cambridge, United Kingdom.ORCID 0000-0002-2675-309X
Stanley E StrawbridgeWellcome Trust-Medical Research Council Stem Cell Institute, Jeffrey Cheah Biomedical Centre, University of Cambridge, CB2 0AW Cambridge, United Kingdom.
Siarhei HladkouWellcome Trust-Medical Research Council Stem Cell Institute, Jeffrey Cheah Biomedical Centre, University of Cambridge, CB2 0AW Cambridge, United Kingdom.ORCID 0000-0002-4354-3270
Hannah T StuartWellcome Trust-Medical Research Council Stem Cell Institute, Jeffrey Cheah Biomedical Centre, University of Cambridge, CB2 0AW Cambridge, United Kingdom.
Thorsten E BoroviakDepartment of Physiology, Development and Neuroscience, University of Cambridge, CB2 3EG Cambridge, United Kingdom.
Jose C R SilvaWellcome Trust-Medical Research Council Stem Cell Institute, Jeffrey Cheah Biomedical Centre, University of Cambridge, CB2 0AW Cambridge, United Kingdom.ORCID 0000-0001-5487-1117
Jennifer NicholsWellcome Trust-Medical Research Council Stem Cell Institute, Jeffrey Cheah Biomedical Centre, University of Cambridge, CB2 0AW Cambridge, United Kingdom; jn270@cam.ac.uk ggs28@cam.ac.uk.ORCID 0000-0002-8650-1388
Wellcome/MRC Cambridge Stem Cell Institute · GBUniversity of Cambridge · GB

Funding

Biotechnology and Biological Sciences Research Council BB/R018588/1Medical Research Council MC_PC_17230Medical Research Council MR/R017735/1Wellcome Trust
6 · The paper itself

Abstract

OCT4 is a fundamental component of the molecular circuitry governing pluripotency in vivo and in vitro. To determine how OCT4 establishes and protects the pluripotent lineage in the embryo, we used comparative single-cell transcriptomics and quantitative immunofluorescence on control and OCT4 null blastocyst inner cell masses at two developmental stages. Surprisingly, activation of most pluripotency-associated transcription factors in the early mouse embryo occurs independently of OCT4, with the exception of the JAK/STAT signaling machinery. Concurrently, OCT4 null inner cell masses ectopically activate a subset of trophectoderm-associated genes. Inspection of metabolic pathways implicates the regulation of rate-limiting glycolytic enzymes by OCT4, consistent with a role in sustaining glycolysis. Furthermore, up-regulation of the lysosomal pathway was specifically detected in OCT4 null embryos. This finding implicates a requirement for OCT4 in the production of normal trophectoderm. Collectively, our findings uncover regulation of cellular metabolism and biophysical properties as mechanisms by which OCT4 instructs pluripotency.

Indexed as

AnimalsBlastocyst Inner Cell MassCell LineageEmbryo, MammalianEmbryonic DevelopmentGene Expression Regulation, DevelopmentalGlycolysisMiceOctamer Transcription Factor-3Pluripotent Stem CellsSignal TransductionSingle-Cell AnalysisSTAT3 Transcription FactorOctamer Transcription Factor-3Pou5f1 protein, mouseStat3 protein, mouseSTAT3 Transcription Factordevelopmental biologymetabolismOCT4single-cell profilingSTAT3 pathway

Identifiers

PMID33452132
PMCPMC7826362
OpenAlexW3119484827

What OpenQuestion holds

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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.