Evidence map›Paper›PMID 32857978›Full record

ArticleStem cell reports2020

Retinoic Acid Accelerates the Specification of Enteric Neural Progenitors from In-Vitro-Derived Neural Crest.

Thomas J R Frith, Antigoni Gogolou, James O S Hackland, Zoe A Hewitt, Harry D Moore, Ivana Barbaric, Nikhil Thapar, Alan J Burns, Peter W Andrews, Anestis Tsakiridis and 1 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

22 citing papers in PubMed, 29 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

11 authors at 3 institutions in 5 countries.

Thomas J R FrithUniversity of Sheffield, Department of Biomedical Science, Sheffield, UK. Electronic address: tom.frith@crick.ac.uk.
Antigoni GogolouUniversity of Sheffield, Department of Biomedical Science, Sheffield, UK.
James O S HacklandThe Center for Stem Cell Biology, Memorial Sloan Kettering Cancer Center, New York, USA.
Zoe A HewittUniversity of Sheffield, Department of Biomedical Science, Sheffield, UK.
Harry D MooreUniversity of Sheffield, Department of Biomedical Science, Sheffield, UK.
Ivana BarbaricUniversity of Sheffield, Department of Biomedical Science, Sheffield, UK.
Nikhil ThaparStem Cells and Regenerative Medicine, UCL Great Ormond Street Institute of Child Health, London, UK; Neurogastroenterology and Motility Unit, Great Ormond Street Hospital, London, UK; Department of Gastroenterology, Hepatology and Liver Transplant, Queensland Children's Hospital, Brisbane, Australia; Prince Abdullah Ben Khalid Celiac Research Chair, College of Medicine, King Saud University, Riyadh, KSA.
Alan J BurnsStem Cells and Regenerative Medicine, UCL Great Ormond Street Institute of Child Health, London, UK; Department of Clinical Genetics, Erasmus University Medical Center, Rotterdam, The Netherlands.
Peter W AndrewsUniversity of Sheffield, Department of Biomedical Science, Sheffield, UK.
Anestis TsakiridisUniversity of Sheffield, Department of Biomedical Science, Sheffield, UK. Electronic address: a.tsakiridis@sheffield.ac.uk.
Conor J McCannStem Cells and Regenerative Medicine, UCL Great Ormond Street Institute of Child Health, London, UK. Electronic address: conor.mccann@ucl.ac.uk.
University of Sheffield · GBGreat Ormond Street Hospital · GBMemorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Medical Research Council MC_PC_14115Medical Research Council MR/R015724/1NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

The enteric nervous system (ENS) is derived primarily from the vagal neural crest, a migratory multipotent cell population emerging from the dorsal neural tube between somites 1 and 7. Defects in the development and function of the ENS cause a range of enteric neuropathies, including Hirschsprung disease. Little is known about the signals that specify early ENS progenitors, limiting progress in the generation of enteric neurons from human pluripotent stem cells (hPSCs) to provide tools for disease modeling and regenerative medicine for enteric neuropathies. We describe the efficient and accelerated generation of ENS progenitors from hPSCs, revealing that retinoic acid is critical for the acquisition of vagal axial identity and early ENS progenitor specification. These ENS progenitors generate enteric neurons in vitro and, following in vivo transplantation, achieved long-term colonization of the ENS in adult mice. Thus, hPSC-derived ENS progenitors may provide the basis for cell therapy for defects in the ENS.

Indexed as

AnimalsCell LineEnteric Nervous SystemHumansMiceNeural CrestNeural Stem CellsNeuronsSignal TransductionTime FactorsTretinoinVagus NerveTretinoincell transplantationembryonic stem cellsenteric nervous systemHirschsprung diseasehumanneural crestpluripotent stem cellsretinoic acid

Identifiers

PMID32857978
PMCPMC7486303
OpenAlexW3081193507

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.