Evidence map›Paper›PMID 25116473›Full record

ArticlePloS one2014

Fgfr1 inactivation in the mouse telencephalon results in impaired maturation of interneurons expressing parvalbumin.

Karen Müller Smith, Maria Elisabetta Maragnoli, Pooja M Phull, Kathy May Tran, Lisha Choubey, Flora M Vaccarino

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

16 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Article
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  5. Activity-dependent neuronal Klotho enhances astrocytic aerobic glycolysis.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2019
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  7. Review
  8. Review
  9. Article
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  12. Induction of specific neuron types by overexpression of single transcription factors.In vitro cellular & developmental biology. Animal · 2016
    Article
  13. Article
  14. Review
  15. FGF Signaling Is Necessary for Neurogenesis in Young Mice and Sufficient to Reverse Its Decline in Old Mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
  16. 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

6 authors at 2 institutions in 1 country.

Karen Müller SmithChild Study Center, Yale University, New Haven, Connecticut, United States of America.
Maria Elisabetta MaragnoliChild Study Center, Yale University, New Haven, Connecticut, United States of America.
Pooja M PhullChild Study Center, Yale University, New Haven, Connecticut, United States of America.
Kathy May TranChild Study Center, Yale University, New Haven, Connecticut, United States of America.
Lisha ChoubeyDepartment of Biology, University of Louisiana at Lafayette, Lafayette, Louisiana, United States of America.
Flora M VaccarinoChild Study Center, Yale University, New Haven, Connecticut, United States of America; Department of Neurobiology, Yale University, New Haven, Connecticut, United States of America; Kavli Institute for Neuroscience, Yale University, New Haven, Connecticut, United States of America.
Yale University · USUniversity of Louisiana at Lafayette · US

Funding

Morphogenesis and Function of the Cerebral CortexR01MH067715 · NIMH · YALE UNIVERSITY · PI VACCARINO, FLORA M · 2004 to 2013
$3.8M
The Role of Astrocytes in Cortical Interneuron DevelopmentK01MH087845 · NIMH · YALE UNIVERSITY · PI SMITH, KAREN MULLER · 2010 to 2013
$654k
NIMH NIH HHS K01 MH087845NIMH NIH HHS K01MH087845NIMH NIH HHS R01 MH067715
6 · The paper itself

Abstract

Fibroblast growth factors (Fgfs) and their receptors (Fgfr) are expressed in the developing and adult CNS. Previous studies demonstrated a decrease in cortical interneurons and locomotor hyperactivity in mice with a conditional Fgfr1 deletion generated in radial glial cells during midneurogenesis (Fgfr1(f/f);hGfapCre+). Here, we report earlier and more extensive inactivation of Fgfr1 in neuroepithelial cells of the CNS (Fgfr1(f/f);NesCre+). Similar to findings in Fgfr1(f/f);hGfapCre+ mice, parvalbumin positive (PV+) cortical interneurons are also decreased in the neocortex of Fgfr1(f/f);NesCre+ mice when compared to control littermates (Fgfr1(f/f)). Fgfr1(f/f);NesCre+ embryos do not differ from controls in the initial specification of GABAergic cells in the ganglionic eminence (GE) as assessed by in situ hybridization for Dlx2, Mash1 and Nkx2. Equal numbers of GABAergic neuron precursors genetically labeled with green fluorescent protein (GFP) were observed at P0 in Fgfr1(f/f);hGfapCre+;Gad1-GFP mutant mice. However, fewer GFP+ and GFP+/PV+ interneurons were observed in these mutants at adulthood, indicating that a decrease in cortical interneuron markers is occurring postnatally. Fgfr1 is expressed in cortical astrocytes in the postnatal brain. To test whether the astrocytes of mice lacking Fgfr1 are less capable of supporting interneurons, we co-cultured wild type Gad1-GFP+ interneuron precursors isolated from the medial GE (MGE) with astrocytes from Fgfr1(f/f) control or Fgfr1(f/f);hGfapCre+ mice. Interneurons grown on Fgfr1 deficient astrocytes had small soma size and fewer neurites per cell, but no differences in cell survival. Decreased soma size of Gad67 immunopositive interneurons was also observed in the cortex of adult Fgfr1(f/f);NesCre+ mice. Our data indicate that astrocytes from Fgfr1 mutants are impaired in supporting the maturation of cortical GABAergic neurons in the postnatal period. This model may elucidate potential mechanisms of impaired PV interneuron maturation relevant to neuropsychiatric disorders that develop in childhood and adolescence.

Indexed as

Gene SilencingAnimalsApoptosisAstrocytesCell CommunicationCell CountCell MovementCell ProliferationCoculture TechniquesGene DeletionGene ExpressionInterneuronsMiceMice, TransgenicMutationParvalbuminsParvalbuminsReceptor, Fibroblast Growth Factor, Type 1

Identifiers

PMID25116473
PMCPMC4130531
OpenAlexW1971860233

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.