Evidence map›Paper›PMID 35902669›Full record

ArticleScientific reports2022

Evidence for oligodendrocyte progenitor cell heterogeneity in the adult mouse brain.

Rebecca M Beiter, Courtney Rivet-Noor, Andrea R Merchak, Robin Bai, David M Johanson, Erica Slogar, Katia Sol-Church, Christopher C Overall, Alban Gaultier

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
7.9field-weighted citation impact, top 1% 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

51 citing papers in PubMed, 69 citations in OpenAlex.

  1. Review
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  8. White matter injury after brain ischemia.Experimental neurology · 2026
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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

9 authors at 1 institution in 1 country.

Rebecca M BeiterDepartment of Neuroscience, Center for Brain Immunology and Glia, University of Virginia School of Medicine, Charlottesville, VA, 22908, USA.
Courtney Rivet-NoorDepartment of Neuroscience, Center for Brain Immunology and Glia, University of Virginia School of Medicine, Charlottesville, VA, 22908, USA.
Andrea R MerchakDepartment of Neuroscience, Center for Brain Immunology and Glia, University of Virginia School of Medicine, Charlottesville, VA, 22908, USA.
Robin BaiDepartment of Neuroscience, Center for Brain Immunology and Glia, University of Virginia School of Medicine, Charlottesville, VA, 22908, USA.
David M JohansonDepartment of Neuroscience, Center for Brain Immunology and Glia, University of Virginia School of Medicine, Charlottesville, VA, 22908, USA.
Erica SlogarDepartment of Neuroscience, Center for Brain Immunology and Glia, University of Virginia School of Medicine, Charlottesville, VA, 22908, USA.
Katia Sol-ChurchGenome Analysis and Technology Core, University of Virginia School of Medicine, Charlottesville, VA, 22908, USA.
Christopher C OverallDepartment of Neuroscience, Center for Brain Immunology and Glia, University of Virginia School of Medicine, Charlottesville, VA, 22908, USA.
Alban GaultierDepartment of Neuroscience, Center for Brain Immunology and Glia, University of Virginia School of Medicine, Charlottesville, VA, 22908, USA. ag7h@virginia.edu.
University of Virginia · US

Funding

Brain, Immunology and Glia Training ProgramT32NS115657 · NINDS · UNIVERSITY OF VIRGINIA · PI Alban P Gaultier, TAJIE H. HARRIS · 2021 to 2026
$1.2M
NOVO-118 as a therapeutic to promote remyelination in in vivo models of MSR41NS110159 · NINDS · NOVORON BIOSCIENCE, INC. · PI GAULTIER, ALBAN P, STILES, TRAVIS LEE · 2019 to 2020
$707k
The role of oligodendrocyte progenitor cells in neuroinflammationR56NS120352 · NINDS · UNIVERSITY OF VIRGINIA · PI GAULTIER, ALBAN P · 2021 to 2021
$463k
Diversity of oligodendrocyte precursor cells in the adult central nervous systemR21NS111204 · NINDS · UNIVERSITY OF VIRGINIA · PI GAULTIER, ALBAN P · 2019 to 2019
$435k
NINDS NIH HHS R21 NS111204NINDS NIH HHS R41 NS110159NINDS NIH HHS R56 NS120352NINDS NIH HHS T32 NS115657
6 · The paper itself

Abstract

Oligodendrocyte progenitor cells (OPCs) account for approximately 5% of the adult brain and have been historically studied for their role in myelination. In the adult brain, OPCs maintain their proliferative capacity and ability to differentiate into oligodendrocytes throughout adulthood, even though relatively few mature oligodendrocytes are produced post-developmental myelination. Recent work has begun to demonstrate that OPCs likely perform multiple functions in both homeostasis and disease and can significantly impact behavioral phenotypes such as food intake and depressive symptoms. However, the exact mechanisms through which OPCs might influence brain function remain unclear. The first step in further exploration of OPC function is to profile the transcriptional repertoire and assess the heterogeneity of adult OPCs. In this work, we demonstrate that adult OPCs are transcriptionally diverse and separate into two distinct populations in the homeostatic brain. These two groups show distinct transcriptional signatures and enrichment of biological processes unique to individual OPC populations. We have validated these OPC populations using multiple methods, including multiplex RNA in situ hybridization and RNA flow cytometry. This study provides an important resource that profiles the transcriptome of adult OPCs and will provide a toolbox for further investigation into novel OPC functions.

Indexed as

Adult Stem CellsOligodendrocyte Precursor CellsAnimalsBrainCell DifferentiationMiceOligodendrogliaRNARNA

Identifiers

PMID35902669
PMCPMC9334628
OpenAlexW4288096154

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.