Evidence map›Paper›PMID 32988384›Full record

ArticleNeural development2020

Individual neuronal subtypes control initial myelin sheath growth and stabilization.

Heather N Nelson, Anthony J Treichel, Erin N Eggum, Madeline R Martell, Amanda J Kaiser, Allie G Trudel, James R Gronseth, Samantha T Maas, Silas Bergen, Jacob H Hines

Open access · goldAbstract read
In one paragraph

Article in Neural development, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 23% 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

11 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. 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

10 authors at 1 institution in 1 country.

Heather N NelsonBiology Department, Winona State University, Winona, MN, USA.
Anthony J TreichelBiology Department, Winona State University, Winona, MN, USA.
Erin N EggumBiology Department, Winona State University, Winona, MN, USA.
Madeline R MartellBiology Department, Winona State University, Winona, MN, USA.
Amanda J KaiserBiology Department, Winona State University, Winona, MN, USA.
Allie G TrudelBiology Department, Winona State University, Winona, MN, USA.
James R GronsethBiology Department, Winona State University, Winona, MN, USA.
Samantha T MaasBiology Department, Winona State University, Winona, MN, USA.
Silas BergenBiology Department, Winona State University, Winona, MN, USA.
Jacob H HinesBiology Department, Winona State University, Winona, MN, USA. jhhines@winona.edu.ORCID 0000-0003-1557-3795
Winona State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn the developing central nervous system, pre-myelinating oligodendrocytes sample candidate nerve axons by extending and retracting process extensions. Some contacts stabilize, leading to the initiation of axon wrapping, nascent myelin sheath formation, concentric wrapping and sheath elongation, and sheath stabilization or pruning by oligodendrocytes. Although axonal signals influence the overall process of myelination, the precise oligodendrocyte behaviors that require signaling from axons are not completely understood. In this study, we investigated whether oligodendrocyte behaviors during the early events of myelination are mediated by an oligodendrocyte-intrinsic myelination program or are over-ridden by axonal factors.

methodsTo address this, we utilized in vivo time-lapse imaging in embryonic and larval zebrafish spinal cord during the initial hours and days of axon wrapping and myelination. Transgenic reporter lines marked individual axon subtypes or oligodendrocyte membranes.

resultsIn the larval zebrafish spinal cord, individual axon subtypes supported distinct nascent sheath growth rates and stabilization frequencies. Oligodendrocytes ensheathed individual axon subtypes at different rates during a two-day period after initial axon wrapping. When descending reticulospinal axons were ablated, local spinal axons supported a constant ensheathment rate despite the increased ratio of oligodendrocytes to target axons.

conclusionWe conclude that properties of individual axon subtypes instruct oligodendrocyte behaviors during initial stages of myelination by differentially controlling nascent sheath growth and stabilization.

Indexed as

AnimalsAnimals, Genetically ModifiedAxonsEmbryo, NonmammalianGenes, ReporterLarvaMyelin SheathOligodendrogliaSpinal CordZebrafishGliaMyelinationMyelin sheathOligodendrocyte

Identifiers

PMID32988384
PMCPMC7523326
OpenAlexW3090304807

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.