Evidence map›Paper›PMID 22248045›Full record

ArticleNeural development2012

Meningeal defects alter the tangential migration of cortical interneurons in Foxc1hith/hith mice.

Konstantinos Zarbalis, Youngshik Choe, Julie A Siegenthaler, Lori A Orosco, Samuel J Pleasure

Open access · goldAbstract read
In one paragraph

Article in Neural development, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.6field-weighted citation impact, top 12% 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

32 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Stuck on you: Meninges cellular crosstalk in development.Current opinion in neurobiology · 2023
    Review
  9. Genomic Landscape of Meningiomas.Advances in experimental medicine and biology · 2023
    Article
  10. Article
  11. Article
  12. FLRT2 and FLRT3 Cooperate in Maintaining the Tangential Migratory Streams of Cortical Interneurons during Development.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  13. Article
  14. Article
  15. Review
  16. Developmental biology of the meninges.Genesis (New York, N.Y. : 2000) · 2019
    Review
  17. Article
  18. Article
  19. Article
  20. Article
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

5 authors at 3 institutions in 1 country.

Konstantinos ZarbalisInstitute of Pediatric Regenerative Medicine Shriners Hospitals for Children, Northern California, 2425 Stockton Blvd., CA 95817, USA. kzarbalis@ucdavis.edu
Youngshik Choe
Julie A Siegenthaler
Lori A Orosco
Samuel J Pleasure
University of California, San Francisco · USShriners Hospitals for Children - Erie · USShriners Hospitals for Children - Northern California · US

Funding

Defective Forebrain Development in Mutant MiceR01DA017627 · NIDA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI PLEASURE, SAMUEL JEREMY · 2003 to 2013
$2.6M
NIDA NIH HHS R01 DA017627
6 · The paper itself

Abstract

backgroundTangential migration presents the primary mode of migration of cortical interneurons translocating into the cerebral cortex from subpallial domains. This migration takes place in multiple streams with the most superficial one located in the cortical marginal zone. While a number of forebrain-expressed molecules regulating this process have emerged, it remains unclear to what extent structures outside the brain, like the forebrain meninges, are involved.

resultsWe studied a unique Foxc1 hypomorph mouse model (Foxc1hith/hith) with meningeal defects and impaired tangential migration of cortical interneurons. We identified a territorial correlation between meningeal defects and disruption of interneuron migration along the adjacent marginal zone in these animals, suggesting that impaired meningeal integrity might be the primary cause for the observed migration defects. Moreover, we postulate that the meningeal factor regulating tangential migration that is affected in homozygote mutants is the chemokine Cxcl12. In addition, by using chromatin immunoprecipitation analysis, we provide evidence that the Cxcl12 gene is a direct transcriptional target of Foxc1 in the meninges. Further, we observe migration defects of a lesser degree in Cajal-Retzius cells migrating within the cortical marginal zone, indicating a less important role for Cxcl12 in their migration. Finally, the developmental migration defects observed in Foxc1hith/hith mutants do not lead to obvious differences in interneuron distribution in the adult if compared to control animals.

conclusionsOur results suggest a critical role for the forebrain meninges to promote during development the tangential migration of cortical interneurons along the cortical marginal zone and Cxcl12 as the factor responsible for this property.

Indexed as

AnimalsCell MovementCerebral CortexChemokine CXCL12Disease Models, AnimalFemaleForkhead Transcription FactorsInterneuronsMaleMeningoceleMiceMice, Inbred C57BLMice, TransgenicNervous System MalformationsPrimary Cell CultureChemokine CXCL12Cxcl12 protein, mouseForkhead Transcription FactorsFoxc1 protein, mouse

Identifiers

PMID22248045
PMCPMC3287125
OpenAlexW1974606737

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.