Evidence map›Paper›PMID 30347186›Full record

ArticleDevelopmental biology2018

Sequential specification of oligodendrocyte lineage cells by distinct levels of Hedgehog and Notch signaling.

Andrew M Ravanelli, Christina A Kearns, Rani K Powers, Yuying Wang, Jacob H Hines, Maranda J Donaldson, Bruce Appel

Abstract read
In one paragraph

Article in Developmental biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed.

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  18. Proteome Profile of Myelin in the Zebrafish Brain.Frontiers in cell and developmental biology · 2021
    Article
  19. Review
  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

7 authors.

Andrew M RavanelliDepartment of Pediatrics, University of Colorado School of Medicine, Aurora, CO 80045, USA.
Christina A KearnsDepartment of Pediatrics, University of Colorado School of Medicine, Aurora, CO 80045, USA.
Rani K PowersDepartment of Pediatrics, University of Colorado School of Medicine, Aurora, CO 80045, USA.
Yuying WangDepartment of Pediatrics, University of Colorado School of Medicine, Aurora, CO 80045, USA.
Jacob H HinesDepartment of Pediatrics, University of Colorado School of Medicine, Aurora, CO 80045, USA.
Maranda J DonaldsonDepartment of Pediatrics, University of Colorado School of Medicine, Aurora, CO 80045, USA.
Bruce AppelDepartment of Pediatrics, University of Colorado School of Medicine, Aurora, CO 80045, USA. Electronic address: bruce.appel@ucdenver.edu.

Funding

Development of Psychopathology, Psychobiology, & BehaviorT32MH015442 · NIMH · UNIVERSITY OF COLORADO DENVER · PI JASON R TREGELLAS · 1985 to 2026
$10.2M
ZEBRAFISH TRANSGENIC CORE - ROCKY MOUNTAIN NEUROLOGICAL DISORDERS CORE CENTERP30NS048154 · NINDS · UNIVERSITY OF COLORADO DENVER · PI RIBERA, ANGELES BADELL · 2004 to 2020
$10.1M
Genetic Analysis of Oligodendrocyte SpecificationR01NS046668 · NINDS · VANDERBILT UNIVERSITY · PI APPEL, BRUCE H · 2004 to 2019
$4.8M
NIMH NIH HHS T32 MH015442NINDS NIH HHS P30 NS048154NINDS NIH HHS R01 NS046668
6 · The paper itself

Abstract

During development of the central nervous system oligodendrocyte precursor cells (OPCs) give rise to both myelinating oligodendrocytes and NG2 glia, which are the most proliferative cells in the adult mammalian brain. NG2 glia retain characteristics of OPCs, and some NG2 glia produce oligodendrocytes, but many others persist throughout adulthood. Why some OPCs differentiate as oligodendrocytes during development whereas others persist as OPCs and acquire characteristics of NG2 glia is not known. Using zebrafish spinal cord as a model, we found that OPCs that differentiate rapidly as oligodendrocytes and others that remain as OPCs arise in sequential waves from distinct neural progenitors. Additionally, oligodendrocyte and persistent OPC fates are specified during a defined critical period by small differences in Shh signaling and Notch activity, which modulates Shh signaling response. Thus, our data indicate that OPCs fated to produce oligodendrocytes or remain as OPCs during development are specified as distinct cell types, raising the possibility that the myelinating potential of OPCs is set by graded Shh signaling activity.

Indexed as

AnimalsBrainCell DifferentiationCell LineageCell ProliferationCentral Nervous SystemHedgehog ProteinsNeurogliaOligodendrocyte Precursor CellsOligodendrogliaReceptors, NotchSignal TransductionSpinal CordStem CellsZebrafishZebrafish ProteinsHedgehog ProteinsReceptors, NotchZebrafish Proteins

Identifiers

PMID30347186
PMCPMC6263812

What OpenQuestion holds

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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.