Evidence map›Paper›PMID 39566199›Full record

ArticleDifferentiation; research in biological diversity

Cspg4 sculpts oligodendrocyte precursor cell morphology.

Samantha Bromley-Coolidge, Diego Iruegas, Bruce Appel

Abstract read
In one paragraph

Article in Differentiation; research in biological diversity. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Samantha Bromley-CoolidgeSection of Developmental Biology, Department of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, CO, 80445, USA.
Diego IruegasSection of Developmental Biology, Department of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, CO, 80445, USA.
Bruce AppelSection of Developmental Biology, Department of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, CO, 80445, USA. Electronic address: bruce.appel@cuanschutz.edu.

Funding

Mechanisms of Developmental MyelinationR35NS122191 · NINDS · UNIVERSITY OF COLORADO DENVER · PI Bruce H Appel · 2021 to 2026
$5.4M
NIH HHS NS406668NINDS NIH HHS R35 NS122191
6 · The paper itself

Abstract

The extracellular matrix (ECM) provides critical biochemical and structural cues that regulate neural development. Chondroitin sulfate proteoglycans (CSPGs), a major ECM component, have been implicated in modulating oligodendrocyte precursor cell (OPC) proliferation, migration, and maturation, but their specific roles in oligodendrocyte lineage cell (OLC) development and myelination in vivo remain poorly understood. Here, we use zebrafish as a model system to investigate the spatiotemporal dynamics of ECM deposition and CSPG localization during central nervous system (CNS) development, with a focus on their relationship to OLCs. We demonstrate that ECM components, including CSPGs, are dynamically expressed in distinct spatiotemporal patterns coinciding with OLC development and myelination. We found that zebrafish lacking cspg4 function produced normal numbers of OLCs, which appeared to undergo proper differentiation. However, OPC morphology in mutant larvae was aberrant. Nevertheless, the number and length of myelin sheaths produced by mature oligodendrocytes were unaffected. These data indicate that Cspg4 regulates OPC morphogenesis in vivo, supporting the role of the ECM in neural development.

Indexed as

Cell DifferentiationMyelin SheathOligodendrocyte Precursor CellsOligodendrogliaZebrafishAnimalsAntigensCentral Nervous SystemChondroitin Sulfate Proteoglycan 4Chondroitin Sulfate ProteoglycansExtracellular MatrixProteoglycansZebrafish ProteinsAntigensChondroitin Sulfate Proteoglycan 4Chondroitin Sulfate ProteoglycansProteoglycansZebrafish ProteinsExtracellular matrixGliaMyelinationNeural cell differentiationNeural cell fateZebrafish

Identifiers

PMID39566199
PMCPMC11637897

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Registered trials

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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.