Evidence map›Paper›PMID 24859004›Full record

ArticleNature cell biology2014

The ability of inner-cell-mass cells to self-renew as embryonic stem cells is acquired following epiblast specification.

Thorsten Boroviak, Remco Loos, Paul Bertone, Austin Smith, Jennifer Nichols

Open access · greenAbstract read
In one paragraph

Article in Nature cell biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 261 papers.

0numbers the graph read from it
0cells of the map it votes in
261citing papers in PubMed
23.2field-weighted citation impact, top 1% 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

261 citing papers in PubMed, 446 citations in OpenAlex.

  1. Article
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201 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 1 country.

Thorsten BoroviakWellcome Trust - Medical Research Council Cambridge Stem Cell Institute, University of Cambridge, Tennis Court Road Cambridge CB2 1QR, UK.
Remco LoosEuropean Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Trust Genome Campus, Cambridge CB10 1SD, UK.
Paul Bertone1] Wellcome Trust - Medical Research Council Cambridge Stem Cell Institute, University of Cambridge, Tennis Court Road Cambridge CB2 1QR, UK [2] European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Trust Genome Campus, Cambridge CB10 1SD, UK [3] Genome Biology and Developmental Biology Units, European Molecular Biology Laboratory, Meyerhofstraße 1, 69117 Heidelberg, Germany.
Austin Smith1] Wellcome Trust - Medical Research Council Cambridge Stem Cell Institute, University of Cambridge, Tennis Court Road Cambridge CB2 1QR, UK [2] Department of Biochemistry, University of Cambridge, Cambridge CB2 1GA, UK.
Jennifer Nichols1] Wellcome Trust - Medical Research Council Cambridge Stem Cell Institute, University of Cambridge, Tennis Court Road Cambridge CB2 1QR, UK [2] Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB2 3EG, UK.
Medical Research Council · GBUniversity of Cambridge · GBEuropean Bioinformatics Institute · GB

Funding

Biotechnology and Biological Sciences Research Council BB/G015678/1Medical Research Council G1001028Medical Research Council G1100526Medical Research Council MC_PC_12009Wellcome Trust 091484
6 · The paper itself

Abstract

The precise relationship of embryonic stem cells (ESCs) to cells in the mouse embryo remains controversial. We present transcriptional and functional data to identify the embryonic counterpart of ESCs. Marker profiling shows that ESCs are distinct from early inner cell mass (ICM) and closely resemble pre-implantation epiblast. A characteristic feature of mouse ESCs is propagation without ERK signalling. Single-cell culture reveals that cell-autonomous capacity to thrive when the ERK pathway is inhibited arises late during blastocyst development and is lost after implantation. The frequency of deriving clonal ESC lines suggests that all E4.5 epiblast cells can become ESCs. We further show that ICM cells from early blastocysts can progress to ERK independence if provided with a specific laminin substrate. These findings suggest that formation of the epiblast coincides with competence for ERK-independent self-renewal in vitro and consequent propagation as ESC lines.

Indexed as

Cell DifferentiationCell LineageCell ProliferationAnimalsBiomarkersBlastocyst Inner Cell MassCell LineClone CellsEmbryo Culture TechniquesEmbryo ImplantationEmbryonic Stem CellsExtracellular Signal-Regulated MAP KinasesGene Expression ProfilingGene Expression Regulation, DevelopmentalGerm LayersGestational AgeBiomarkersExtracellular Signal-Regulated MAP KinasesLamininTranscription Factors

Identifiers

PMID24859004
PMCPMC4878656
OpenAlexW2074591015

What OpenQuestion holds

Textmetadata
LicenceTDM
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.