Evidence map›Paper›PMID 39688302›Full record

ArticleGlia2025

Axonal Selectivity of Myelination by Single Oligodendrocytes Established During Development in Mouse Cerebellar White Matter.

Batpurev Battulga, Yasuyuki Osanai, Reiji Yamazaki, Yoshiaki Shinohara, Nobuhiko Ohno

Abstract read
In one paragraph

Article in Glia, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Glial Cells and Aging: From the CNS to the Cerebellum.International journal of molecular sciences · 2025
    Review
  4. 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.

Batpurev BattulgaDivision of Histology and Cell Biology, Department of Anatomy, School of Medicine, Jichi Medical University, Shimotsuke, Japan.ORCID 0000-0002-7709-4557
Yasuyuki OsanaiDivision of Histology and Cell Biology, Department of Anatomy, School of Medicine, Jichi Medical University, Shimotsuke, Japan.ORCID 0000-0001-7285-7546
Reiji YamazakiDivision of Histology and Cell Biology, Department of Anatomy, School of Medicine, Jichi Medical University, Shimotsuke, Japan.ORCID 0000-0001-8052-6624
Yoshiaki ShinoharaDivision of Histology and Cell Biology, Department of Anatomy, School of Medicine, Jichi Medical University, Shimotsuke, Japan.ORCID 0000-0002-8975-4604
Nobuhiko OhnoDivision of Histology and Cell Biology, Department of Anatomy, School of Medicine, Jichi Medical University, Shimotsuke, Japan.ORCID 0000-0002-6536-2753

Funding

Japan Society for the Promotion of Science 20KK0170Japan Society for the Promotion of Science 21H04786Japan Society for the Promotion of Science 21H05241Japan Society for the Promotion of Science 21K15197Japan Society for the Promotion of Science 24H00583National Center of Neurology and Psychiatry 3-5Uehara Memorial Foundation 202210148
6 · The paper itself

Abstract

Myelin formation by oligodendrocytes regulates the conduction velocity and functional integrity of neuronal axons. While individual oligodendrocytes form myelin sheaths around multiple axons and control the functions of neural circuits where the axons are involved, it remains unclear if oligodendrocytes selectively form myelin sheaths around specific subtypes of axons. Using the combination of rabies virus-mediated single oligodendrocyte labeling and immunostaining with tissue clearing, we revealed that approximately half of the oligodendrocytes preferentially myelinate axons originating from Purkinje cells in the white matter of adult mouse cerebella. The preference for Purkinje cell axons was more pronounced during development when the process of myelination within cerebellar white matter was initiated; over 90% of oligodendrocytes preferentially myelinated Purkinje cell axons. Preferential myelination of Purkinje cell axons was further confirmed by immuno-electron microscopy and transgenic mice that label early-born oligodendrocytes. Transgenic mice that label oligodendrocytes differentiated at the early development showed that early-born oligodendrocytes preferentially myelinate Purkinje cell axons in the matured cerebellar white matter. In contrast, transgenic mice that label oligodendrocytes differentiated after the peak of cerebellar myelination showed that the later-differentiated oligodendrocytes dominantly myelinated non-Purkinje cell axons. These results demonstrate that a significant proportion of oligodendrocytes preferentially myelinate functionally distinct axons in the cerebellar white matter, and the axonal preference of myelination by individual oligodendrocytes is established depending on the timing of their differentiation during development. Our data provide the evidence that there is a critical time window of myelination that a specific subtype of axons are dominantly myelinated by the oligodendrocytes.

Indexed as

AxonsCerebellumMyelin SheathNerve Fibers, MyelinatedOligodendrogliaWhite MatterAnimalsCell DifferentiationMiceMice, Inbred C57BLMice, TransgenicPurkinje CellscerebellummyelinneurodevelopmentoligodendrocytePurkinje cell

Identifiers

PMID39688302
PMCPMC11845844

What OpenQuestion holds

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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.