Evidence map›Paper›PMID 25127137›Full record

ArticleCell reports2014

Gli3 repressor controls cell fates and cell adhesion for proper establishment of neurogenic niche.

Hui Wang, Anna W Kane, Cheol Lee, Sohyun Ahn

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

25 citing papers in PubMed, 32 citations in OpenAlex.

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  6. Impaired Blastocyst Formation inInternational journal of molecular sciences · 2023
    Article
  7. Ontogeny of adult neural stem cells in the mammalian brain.Current topics in developmental biology · 2021
    Review
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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

4 authors at 3 institutions in 1 country.

Hui WangProgram in Genomics of Differentiation, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.
Anna W KaneProgram in Genomics of Differentiation, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA; Brown-NIH Graduate Partnership Program, Department of Neuroscience, Brown University, Providence, RI 02912, USA.
Cheol LeeProgram in Genomics of Differentiation, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.
Sohyun AhnProgram in Genomics of Differentiation, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA. Electronic address: ahnsohyun@mail.nih.gov.
National Institutes of Health · USBrown University · USEunice Kennedy Shriver National Institute of Child Health and Human Development · US

Funding

Molecular Genetics of Neural Stem CellsZIAHD008781 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI AHN, SOHYUN · 2009 to 2014
$4.2M
Intramural NIH HHS ZIA HD008781PHS HHS 1ZIHD008781
6 · The paper itself

Abstract

Neural stem cells (NSCs) in the subventricular zone (SVZ) rely on environmental signals provided by the neurogenic niche for their proper function. However, little is known about the initial steps of niche establishment, as embryonic radial glia transition to postnatal NSCs. Here, we identify Gli3 repressor (Gli3R), a component of the Sonic hedgehog (Shh) pathway, as a critical factor controlling both cell-type specification and structural organization of the developing SVZ. We demonstrate that Gli3R expressed in radial glia temporally regulates gp130/STAT3 signaling at the transcriptional level to suppress glial characteristics in differentiating ependymal cells. In addition, Gli3R maintains the proper level of Numb in ependymal cells to allow localization of cell adhesion molecules such as vascular cell adhesion molecule (VCAM) and E-cadherin. Thus, our findings reveal a role for Gli3R as a mediator of niche establishment and provide insights into the conditions required for proper SVZ neurogenic niche formation.

Indexed as

Stem Cell NicheAnimalsBase SequenceCarrier ProteinsCell AdhesionCerebral VentriclesCytokine Receptor gp130FemaleGene ExpressionGlial Fibrillary Acidic ProteinIntracellular Signaling Peptides and ProteinsKruppel-Like Transcription FactorsMice, TransgenicNerve Tissue ProteinsNeural Stem CellsNeurogenesisCarrier ProteinsCytokine Receptor gp130Gli3 protein, mouseGlial Fibrillary Acidic Proteinglial fibrillary astrocytic protein, mouseIl6st protein, mouseIntracellular Signaling Peptides and ProteinsKruppel-Like Transcription FactorsLnx2 protein, mouseNerve Tissue ProteinsStat3 protein, mouseSTAT3 Transcription FactorZinc Finger Protein Gli3

Identifiers

PMID25127137
PMCPMC4151506
OpenAlexW2025915218

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.