Evidence map›Paper›PMID 15509736›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2004

Fibroblast growth factor receptor signaling promotes radial glial identity and interacts with Notch1 signaling in telencephalic progenitors.

Keejung Yoon, Susana Nery, Michael L Rutlin, Freddy Radtke, Gord Fishell, Nicholas Gaiano

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
4.9field-weighted citation impact, top 5% 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

77 citing papers in PubMed, 188 citations in OpenAlex.

  1. Article
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  3. Review
  4. Article
  5. Article
  6. Article
  7. Functional Divergence ofInternational journal of molecular sciences · 2025
    Article
  8. Review
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  10. Article
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  13. Article
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  15. Article
  16. The Emerging Role of the FGF/FGFR Pathway in Gastrointestinal Stromal Tumor.International journal of molecular sciences · 2020
    Review
  17. FGFR- gene family alterations in low-grade neuroepithelial tumors.Acta neuropathologica communications · 2020
    Review
  18. Article
  19. Article
  20. Review

17 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

6 authors at 4 institutions in 3 countries.

Keejung YoonInstitute for Cell Engineering, Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.
Susana Nery
Michael L Rutlin
Freddy Radtke
Gord Fishell
Nicholas Gaiano
Johns Hopkins University · USNew York University · USGenomics (United Kingdom) · GBLudwig Cancer Research · CH

Funding

MECHANISMS OF NEURAL PATTERNING IN MAMMALIAN FOREBRAINR01NS032993 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI FISHELL, GORDON J · 1995 to 2007
$2.9M
NINDS NIH HHS NS32993NINDS NIH HHS R01 NS032993
6 · The paper itself

Abstract

The Notch and fibroblast growth factor (FGF) pathways both regulate cell fate specification during mammalian neural development. We have shown previously that Notch1 activation in the murine forebrain promotes radial glial identity. This result, together with recent evidence that radial glia can be progenitors, suggested that Notch1 signaling might promote progenitor and radial glial character simultaneously. Consistent with this idea, we found that in addition to promoting radial glial character in vivo, activated Notch1 (ActN1) increased the frequency of embryonic day 14.5 (E14.5) ganglionic eminence (GE) progenitors that grew into neurospheres in FGF2. Constitutive activation of C-promoter binding factor (CBF1), a Notch pathway effector, also increased neurosphere frequency in FGF2, suggesting that the effect of Notch1 on FGF responsiveness is mediated by CBF1. The observation that ActN1 promoted FGF responsiveness in telencephalic progenitors prompted us to examine the effect of FGF pathway activation in vivo. We focused on FGFR2 because it is expressed in radial glia in the GEs where ActN1 increases FGF2 neurosphere frequency, but not in the septum where it does not. Like ActN1, activated FGFR2 (ActFGFR2) promoted radial glial character in vivo. However, unlike ActN1, ActFGFR2 did not enhance neurosphere frequency at E14.5. Additional analysis demonstrated that, unexpectedly, neither ActFGFR2 nor ActFGFR1 could replace the need for ligand in promoting neurosphere proliferation. This study suggests that telencephalic progenitors with radial glial morphology are maintained by interactions between the Notch and FGF pathways, and that the mechanisms by which FGF signaling promotes radial glial character in vivo and progenitor proliferation in vitro can be uncoupled.

Indexed as

AnimalsCell ProliferationDNA-Binding ProteinsEpidermal Growth FactorFibroblast Growth Factor 2Immunoglobulin J Recombination Signal Sequence-Binding ProteinMiceMice, KnockoutNerve Tissue ProteinsNeurogliaNuclear ProteinsReceptor, Notch1Receptors, Cell SurfaceReceptors, Fibroblast Growth FactorRecombinant Fusion ProteinsSignal TransductionDNA-Binding ProteinsEpidermal Growth FactorFibroblast Growth Factor 2Immunoglobulin J Recombination Signal Sequence-Binding ProteinNerve Tissue ProteinsNotch1 protein, mouseNuclear ProteinsRbpj protein, mouseReceptor, Notch1Receptors, Cell SurfaceReceptors, Fibroblast Growth FactorRecombinant Fusion ProteinsTranscription Factors

Identifiers

PMID15509736
PMCPMC6730142
OpenAlexW2089558318

What OpenQuestion holds

Textmetadata
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.