Evidence map›Paper›PMID 30095409›Full record

ArticleeLife2018

Human axial progenitors generate trunk neural crest cells in vitro.

Thomas Jr Frith, Ilaria Granata, Matthew Wind, Erin Stout, Oliver Thompson, Katrin Neumann, Dylan Stavish, Paul R Heath, Daniel Ortmann, James Os Hackland and 9 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 1 pooled it
4.9field-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

61 citing papers in PubMed, 1 synthesis or guideline pooled it, 115 citations in OpenAlex.

  1. Pooled it
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  12. From neural crest migration to the onset of gangliogenesis.Current topics in developmental biology · 2025
    Review
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1 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

19 authors at 7 institutions in 3 countries.

Thomas Jr FrithCentre for Stem Cell Biology, Department of Biomedical Science, The University of Sheffield, Sheffield, United Kingdom.ORCID https://orcid.org/0000-0002-6078-5466
Ilaria GranataComputational and Data Science Laboratory, High Performance Computing and Networking Institute, National Research Council of Italy, Napoli, Italy.
Matthew WindCentre for Stem Cell Biology, Department of Biomedical Science, The University of Sheffield, Sheffield, United Kingdom.
Erin StoutCentre for Stem Cell Biology, Department of Biomedical Science, The University of Sheffield, Sheffield, United Kingdom.
Oliver ThompsonCentre for Stem Cell Biology, Department of Biomedical Science, The University of Sheffield, Sheffield, United Kingdom.
Katrin NeumannStem Cell Engineering, Biotechnology Center, Technische Universität Dresden, Dresden, Germany.
Dylan StavishCentre for Stem Cell Biology, Department of Biomedical Science, The University of Sheffield, Sheffield, United Kingdom.
Paul R HeathSheffield Institute for Translational Neuroscience, University of Sheffield, Sheffield, United Kingdom.
Daniel OrtmannAnne McLaren Laboratory, Wellcome Trust-MRC Stem Cell Institute, University of Cambridge, Cambridge, United Kingdom.
James Os HacklandCentre for Stem Cell Biology, Department of Biomedical Science, The University of Sheffield, Sheffield, United Kingdom.ORCID https://orcid.org/0000-0001-7087-9995
Konstantinos AnastassiadisStem Cell Engineering, Biotechnology Center, Technische Universität Dresden, Dresden, Germany.ORCID http://orcid.org/0000-0002-9814-0559
Mina GoutiMax Delbrück Center for Molecular Medicine, Berlin, Germany.
James BriscoeThe Francis Crick Institute, London, United Kingdom.ORCID http://orcid.org/0000-0002-1020-5240
Valerie WilsonMRC Centre for Regenerative Medicine, Institute for Stem Cell Research, School of Biological Sciences, University of Edinburgh, Edinburgh, United Kingdom.ORCID http://orcid.org/0000-0003-4182-5159
Stuart L JohnsonDepartment of Biomedical Science, University of Sheffield, Sheffield, United Kingdom.
Marysia PlaczekDepartment of Biomedical Science, University of Sheffield, Sheffield, United Kingdom.
Mario R GuarracinoComputational and Data Science Laboratory, High Performance Computing and Networking Institute, National Research Council of Italy, Napoli, Italy.
Peter W AndrewsCentre for Stem Cell Biology, Department of Biomedical Science, The University of Sheffield, Sheffield, United Kingdom.
Anestis TsakiridisCentre for Stem Cell Biology, Department of Biomedical Science, The University of Sheffield, Sheffield, United Kingdom.ORCID http://orcid.org/0000-0002-2184-2990
University of Sheffield · GBInstitute for High Performance Computing and Networking · ITTechnische Universität Dresden · DEMax Delbrück Center · DEMRC Centre for Regenerative Medicine · GBThe Francis Crick Institute · GBWellcome/MRC Cambridge Stem Cell Institute · GB

Funding

Biotechnology and Biological Sciences Research Council BB/J015539/1Biotechnology and Biological Sciences Research Council BB/P000444/1Cancer Research UK FC001051Little Princess Trust and Children's Cancer and Leukaemia Group CCLGA 2016 01Medical Research Council MC_PC_12009Medical Research Council MC_PC_14115Medical Research Council Mr/K011200/1Medical Research Council MR/K017047/1Ministero dell'Istruzione, dell'Università e della Ricerca Iteromics Flagship projectRoyal Society RG160249Royal Society University Research FellowSeventh Framework Programme FP7/2007-2013 agreement no. 602423 (Plurimes)Seventh Framework Programme PlurimesUniversity of Sheffield Biomedical Science Departmental PhD studentshipWellcome Trust FC001051
6 · The paper itself

Abstract

The neural crest (NC) is a multipotent embryonic cell population that generates distinct cell types in an axial position-dependent manner. The production of NC cells from human pluripotent stem cells (hPSCs) is a valuable approach to study human NC biology. However, the origin of human trunk NC remains undefined and current in vitro differentiation strategies induce only a modest yield of trunk NC cells. Here we show that hPSC-derived axial progenitors, the posteriorly-located drivers of embryonic axis elongation, give rise to trunk NC cells and their derivatives. Moreover, we define the molecular signatures associated with the emergence of human NC cells of distinct axial identities in vitro. Collectively, our findings indicate that there are two routes toward a human post-cranial NC state: the birth of cardiac and vagal NC is facilitated by retinoic acid-induced posteriorisation of an anterior precursor whereas trunk NC arises within a pool of posterior axial progenitors.

Indexed as

Cell DifferentiationBiomarkersCells, CulturedHumansNeural CrestPluripotent Stem CellsBiomarkersaxial progenitorsdevelopmental biologyembryonic developmenthumanIn vitro differentiationneural crestneuromesodermal progenitorspluripotent stem cellsregenerative medicinestem cells

Identifiers

PMID30095409
PMCPMC6101942
OpenAlexW2886748056

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.