Evidence map›Paper›PMID 25753817›Full record

ArticleStem cells (Dayton, Ohio)2015

Multipotent caudal neural progenitors derived from human pluripotent stem cells that give rise to lineages of the central and peripheral nervous system.

Mark Denham, Kouichi Hasegawa, Trevelyan Menheniott, Ben Rollo, Dongcheng Zhang, Shelley Hough, Abdullah Alshawaf, Fabia Febbraro, Samiramis Ighaniyan, Jessie Leung and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

51 citing papers in PubMed, 86 citations in OpenAlex.

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  20. Studying human nociceptors: from fundamentals to clinic.Brain : a journal of neurology · 2021
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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

14 authors at 5 institutions in 4 countries.

Mark DenhamDepartment of Anatomy and Neurosciences, University of Melbourne, Melbourne, Australia.
Kouichi HasegawaInstitute for Integrated Cell-Material Sciences, Kyoto University, Kyoto, Japan.
Trevelyan MenheniottMurdoch Children's Research Institute, Melbourne, Australia.
Ben RolloMurdoch Children's Research Institute, Melbourne, Australia.
Dongcheng ZhangMurdoch Children's Research Institute, Melbourne, Australia.
Shelley HoughDepartment of Anatomy and Neurosciences, University of Melbourne, Melbourne, Australia.
Abdullah AlshawafCentre for Neural Engineering, Department of Electrical and Electronic Engineering, University of Melbourne, Melbourne, Australia.
Fabia FebbraroDanish Research Institute of Translational Neuroscience, Aarhus University, Aarhus, Denmark.
Samiramis IghaniyanMurdoch Children's Research Institute, Melbourne, Australia.
Jessie LeungDepartment of Anatomy and Neurosciences, University of Melbourne, Melbourne, Australia.
David A ElliottMurdoch Children's Research Institute, Melbourne, Australia.
Donald F NewgreenMurdoch Children's Research Institute, Melbourne, Australia.
Martin F PeraDepartment of Anatomy and Neurosciences, University of Melbourne, Melbourne, Australia.
Mirella DottoriDepartment of Anatomy and Neurosciences, University of Melbourne, Melbourne, Australia.
Murdoch Children's Research Institute · AUUniversity of Melbourne · AUAarhus University · DKKyoto University · JPWalter and Eliza Hall Institute of Medical Research · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The caudal neural plate is a distinct region of the embryo that gives rise to major progenitor lineages of the developing central and peripheral nervous system, including neural crest and floor plate cells. We show that dual inhibition of the glycogen synthase kinase 3β and activin/nodal pathways by small molecules differentiate human pluripotent stem cells (hPSCs) directly into a preneuroepithelial progenitor population we named "caudal neural progenitors" (CNPs). CNPs coexpress caudal neural plate and mesoderm markers, and, share high similarities to embryonic caudal neural plate cells in their lineage differentiation potential. Exposure of CNPs to BMP2/4, sonic hedgehog, or FGF2 signaling efficiently directs their fate to neural crest/roof plate cells, floor plate cells, and caudally specified neuroepithelial cells, respectively. Neural crest derived from CNPs differentiated to neural crest derivatives and demonstrated extensive migratory properties in vivo. Importantly, we also determined the key extrinsic factors specifying CNPs from human embryonic stem cell include FGF8, canonical WNT, and IGF1. Our studies are the first to identify a multipotent neural progenitor derived from hPSCs, that is the precursor for major neural lineages of the embryonic caudal neural tube.

Indexed as

Cell LineageAnimalsCell DifferentiationCentral Nervous SystemMesodermMice, Inbred C57BLNeural CrestNeural PlateNeural Stem CellsNeural TubeNeuroepithelial CellsPeripheral Nervous SystemPluripotent Stem CellsRats, Sprague-DawleyFloor plateHuman embryonic stem cellsNeural crestPeripheral nervous systemRoof plate

Identifiers

PMID25753817
PMCPMC5347855
OpenAlexW1537836582

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.