Evidence map›Paper›PMID 29452604›Full record

ArticleNeural development2018

Transcriptional regulation of ependymal cell maturation within the postnatal brain.

Diana Vidovic, Raul Ayala Davila, Richard M Gronostajski, Tracey J Harvey, Michael Piper

Open access · goldAbstract read
In one paragraph

Article in Neural development, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

15 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
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  10. Hydrocephalus inCells · 2022
    Article
  11. Review
  12. Ependymal Cilia: Physiology and Role in Hydrocephalus.Frontiers in molecular neuroscience · 2022
    Review
  13. Review
  14. Article
  15. 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 2 institutions in 2 countries.

Diana VidovicThe School of Biomedical Sciences, The University of Queensland, Brisbane, QLD, 4072, Australia.
Raul Ayala DavilaThe School of Biomedical Sciences, The University of Queensland, Brisbane, QLD, 4072, Australia.
Richard M GronostajskiDepartment of Biochemistry, Program in Genetics, Genomics and Bioinformatics, Center of Excellence in Bioinformatics and Life Sciences, State University of New York at Buffalo, Buffalo, New York, 14260, USA.
Tracey J HarveyThe School of Biomedical Sciences, The University of Queensland, Brisbane, QLD, 4072, Australia.
Michael PiperThe School of Biomedical Sciences, The University of Queensland, Brisbane, QLD, 4072, Australia. m.piper@uq.edu.au.ORCID 0000-0002-6759-2560
The University of Queensland · AUUniversity at Buffalo, State University of New York · US

Funding

Australian Research Council DP160100368
6 · The paper itself

Abstract

backgroundRadial glial stem cells within the developing nervous system generate a variety of post-mitotic cells, including neurons and glial cells, as well as the specialised multi-ciliated cells that line the walls of the ventricular system, the ependymal cells. Ependymal cells separate the brain parenchyma from the cerebrospinal fluid and mediate osmotic regulation, the flow of cerebrospinal fluid, and the subsequent dispersion of signalling molecules via the co-ordinated beating of their cilia. Deficits to ependymal cell development and function have been implicated in the formation of hydrocephalus, but the transcriptional mechanisms underpinning ependymal development remain poorly characterised.

findingsHere, we demonstrate that the transcription factor nuclear factor IX (NFIX) plays a central role in the development of the ependymal cell layer of the lateral ventricles. Expression of ependymal cell-specific markers is delayed in the absence of Nfix. Moreover, Nfix-deficient mice exhibit aberrant ependymal cell morphology at postnatal day 15, culminating in abnormal thickening and intermittent loss of this cell layer. Finally, we reveal Foxj1, a key factor promoting ependymal cell maturation, as a target for NFIX-mediated transcriptional activation.

conclusionsCollectively, our data indicate that ependymal cell development is reliant, at least in part, on NFIX expression, further implicating this transcription factor as a mediator of multiple aspects of radial glial biology during corticogenesis.

Indexed as

Age FactorsAnalysis of VarianceAnimalsAnimals, NewbornBrainCadherinsChromatin ImmunoprecipitationEpendymaForkhead Transcription FactorsGene Expression Regulation, DevelopmentalMiceMice, Inbred C57BLMice, TransgenicMicroscopy, ConfocalNerve Tissue ProteinsNeurogliaCadherinsCdh2 protein, mouseForkhead Transcription FactorsFOXJ1 protein, mouseNerve Tissue ProteinsNFI Transcription FactorsNfix protein, mouseTranscription FactorsCerebral cortexEpendymal cellNFIXRadial gliaTranscription factor

Identifiers

PMID29452604
PMCPMC5816376
OpenAlexW2794459165

What OpenQuestion holds

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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.