Evidence map›Paper›PMID 25889070›Full record

ArticleNeural development2015

Fgf signaling controls the telencephalic distribution of Fgf-expressing progenitors generated in the rostral patterning center.

Renée V Hoch, Jeffrey A Clarke, John L R Rubenstein

Abstract read
In one paragraph

Article in Neural development, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
–field-weighted citation impact
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

29 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. ERK signaling expands mammalian cortical radial glial cells and extends the neurogenic period.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  7. Cells · 2023
    Article
  8. Fgf8Neuroscience bulletin · 2023
    Article
  9. Review
  10. Article
  11. Single cell enhancer activity distinguishes GABAergic and cholinergic lineages in embryonic mouse basal ganglia.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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

3 authors.

Renée V HochDepartment of Psychiatry, University of California, 1550 4th Street, UCSF MC 2611, San Francisco, CA, 94158, USA. rhoch@plos.org.
Jeffrey A ClarkeDepartment of Psychiatry, University of California, 1550 4th Street, UCSF MC 2611, San Francisco, CA, 94158, USA. jefclarke@gmail.com.
John L R RubensteinDepartment of Psychiatry, University of California, 1550 4th Street, UCSF MC 2611, San Francisco, CA, 94158, USA. john.rubenstein@ucsf.edu.

Funding

Genetic Studies of Cortex Structure and DevelopmentR01NS099099 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI RUBENSTEIN, JOHN L. R. · 2016 to 2025
$6.4M
Genetic Regulation of Telencephalon DevelopmentR37MH049428 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI RUBENSTEIN, JOHN L. R. · 2008 to 2017
$5.9M
GENETIC STUDIES OF CORTEX STRUCTURE AND DEVELOPMENTR01NS034661 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI RUBENSTEIN, JOHN L. R. · 1996 to 2015
$4.6M
Analysis of Fgf17 roles and regulation in mammalian forebrain developmentF32MH081431 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HOCH, RENEE VICTORIA · 2008 to 2010
$104k
NIMH NIH HHS F32 MH081431NIMH NIH HHS F32MH081431NIMH NIH HHS R37 MH049428NINDS NIH HHS R01 NS034661NINDS NIH HHS R01 NS099099NINDS NIH HHS R01 NS34661
6 · The paper itself

Abstract

backgroundThe rostral patterning center (RPC) secretes multiple fibroblast growth factors (Fgfs) essential for telencephalon growth and patterning. Fgf expression patterns suggest that they mark functionally distinct RPC subdomains. We generated Fgf8(CreER) and Fgf17(CreER) mice and used them to analyze the lineages of Fgf8- versus Fgf17-expressing RPC cells.

resultsBoth lineages contributed to medial structures of the rostroventral telencephalon structures including the septum and medial prefrontral cortex. In addition, RPC-derived progenitors were observed in other regions of the early telencephalic neuroepithelium and generated neurons in the olfactory bulb, neocortex, and basal ganglia. Surprisingly, Fgf8(+) RPC progenitors generated the majority of basal ganglia cholinergic neurons. Compared to the Fgf8 lineage, the Fgf17 lineage was more restricted in its early dispersion and its contributions to the telencephalon. Mutant studies suggested that Fgf8 and Fgf17 restrict spread of RPC progenitor subpopulations.

conclusionsWe identified the RPC as an important source of progenitors that contribute broadly to the telencephalon and found that two molecularly distinct progenitor subtypes in the RPC make different contributions to the developing forebrain.

Indexed as

AnimalsBasal GangliaBody PatterningCell LineageCholinergic NeuronsFibroblast Growth Factor 8Fibroblast Growth FactorsGene Expression Regulation, DevelopmentalGene Knock-In TechniquesGenes, SyntheticGestational AgeMiceNeural Stem CellsOlfactory BulbProsencephalonRecombinant Fusion ProteinsFgf17 protein, mouseFgf8 protein, mouseFibroblast Growth Factor 8Fibroblast Growth FactorsRecombinant Fusion Proteins

Identifiers

PMID25889070
PMCPMC4416298

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Registered trials

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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.