Evidence map›Paper›PMID 27671872›Full record

ArticleDevelopmental biology2016

Cerebrovascular defects in Foxc1 mutants correlate with aberrant WNT and VEGF-A pathways downstream of retinoic acid from the meninges.

Swati Mishra, Youngshik Choe, Samuel J Pleasure, Julie A Siegenthaler

Open access · greenAbstract read
In one paragraph

Article in Developmental biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
3.7field-weighted citation impact, top 7% 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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 50 citations in OpenAlex.

  1. Pooled it
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  4. Review
  5. Review
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  7. Article
  8. Article
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  11. Article
  12. Article
  13. Stuck on you: Meninges cellular crosstalk in development.Current opinion in neurobiology · 2023
    Review
  14. Article
  15. Cranium growth, patterning and homeostasis.Development (Cambridge, England) · 2022
    Article
  16. Article
  17. Article
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  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

4 authors at 2 institutions in 1 country.

Swati MishraDepartment of Pediatrics, Section of Developmental Biology, University of Colorado, School of Medicine Aurora, CO 80045, USA.
Youngshik ChoeDepartment of Neurology, Programs in Neuroscience and Developmental Biology, Institute for Regenerative Medicine, UC San Francisco, San Francisco, CA 94158, USA.
Samuel J PleasureDepartment of Neurology, Programs in Neuroscience and Developmental Biology, Institute for Regenerative Medicine, UC San Francisco, San Francisco, CA 94158, USA.
Julie A SiegenthalerDepartment of Pediatrics, Section of Developmental Biology, University of Colorado, School of Medicine Aurora, CO 80045, USA. Electronic address: julie.siegenthaler@ucdenver.edu.
University of California, San Francisco · USUniversity of Colorado Denver · US

Funding

SDF1/CXCR4 Signaling and Tangential Neuronal Migration in the Developing CortexR01MH077694 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI PLEASURE, SAMUEL JEREMY · 2007 to 2019
$5.0M
Retinoic Acid in Development of CNS VasculatureR01NS098273 · NINDS · UNIVERSITY OF COLORADO DENVER · PI SIEGENTHALER, JULIE · 2016 to 2025
$3.2M
Defective Forebrain Development in Mutant MiceR01DA017627 · NIDA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI PLEASURE, SAMUEL JEREMY · 2003 to 2013
$2.6M
Defective Forebrain Development in Mutant MiceR01MH105360 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI PLEASURE, SAMUEL JEREMY · 2014 to 2015
$790k
Forebrain angiogenesis in Foxc1 mutant miceR00NS070920 · NINDS · UNIVERSITY OF COLORADO DENVER · PI SIEGENTHALER, JULIE · 2012 to 2014
$736k
Forebrain angiogenesis in Foxc1 mutant miceK99NS070920 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SIEGENTHALER, JULIE · 2010 to 2011
$156k
NIDA NIH HHS R01 DA017627NIMH NIH HHS R01 MH077694NIMH NIH HHS R01 MH105360NINDS NIH HHS K99 NS070920NINDS NIH HHS R00 NS070920NINDS NIH HHS R01 NS098273
6 · The paper itself

Abstract

Growth and maturation of the cerebrovasculature is a vital event in neocortical development however mechanisms that control cerebrovascular development remain poorly understood. Mutations in or deletions that include the FOXC1 gene are associated with congenital cerebrovascular anomalies and increased stroke risk in patients. Foxc1 mutant mice display severe cerebrovascular hemorrhage at late gestational ages. While these data demonstrate Foxc1 is required for cerebrovascular development, its broad expression in the brain vasculature combined with Foxc1 mutant's complex developmental defects have made it difficult to pinpoint its function(s). Using global and conditional Foxc1 mutants, we find 1) significant cerebrovascular growth defects precede cerebral hemorrhage and 2) expression of Foxc1 in neural crest-derived meninges and brain pericytes, though not endothelial cells, is required for normal cerebrovascular development. We provide evidence that reduced levels of meninges-derived retinoic acid (RA), caused by defects in meninges formation in Foxc1 mutants, is a major contributing factor to the cerebrovascular growth defects in Foxc1 mutants. We provide data that suggests that meninges-derived RA ensures adequate growth of the neocortical vasculature via regulating expression of WNT pathway proteins and neural progenitor derived-VEGF-A. Our findings offer the first evidence for a role of the meninges in brain vascular development and provide new insight into potential causes of cerebrovascular defects in patients with FOXC1 mutations.

Indexed as

Signal TransductionAnimalsbeta-GalactosidaseBlood VesselsBrainCells, CulturedCerebral HemorrhageEmbryo, MammalianEndothelial CellsForkhead Transcription FactorsImmunohistochemistryIntegrasesMeningesMiceMutationNeocortexbeta-GalactosidaseCre recombinaseForkhead Transcription FactorsFoxc1 protein, mouseIntegrasesTretinoinVascular Endothelial Growth Factor AWnt ProteinsCerebrovascular developmentEndothelial cellFoxc1MeningesVEGFWNT

Identifiers

PMID27671872
PMCPMC5124406
OpenAlexW2522819229

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.