Evidence map›Paper›PMID 40548375›Full record

ArticleJCI insight2025

Dysregulated synaptic gene expression in oligodendrocytes of spinal and bulbar muscular atrophy.

Madoka Iida, Kentaro Sahashi, Tomoki Hirunagi, Kenji Sakakibara, Kentaro Maeda, Yohei Iguchi, Jiayi Li, Yosuke Ogura, Masaki Iizuka, Tomohiro Akashi and 5 more

Abstract read
In one paragraph

Article in JCI insight, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

15 authors.

Madoka IidaDepartment of Neurology, Nagoya University Graduate School of Medicine, Showa-ku, Nagoya, Aichi, Japan.
Kentaro SahashiDepartment of Neurology, Nagoya University Graduate School of Medicine, Showa-ku, Nagoya, Aichi, Japan.
Tomoki HirunagiDepartment of Neurology, Nagoya University Graduate School of Medicine, Showa-ku, Nagoya, Aichi, Japan.
Kenji SakakibaraDepartment of Neurology, Nagoya University Graduate School of Medicine, Showa-ku, Nagoya, Aichi, Japan.
Kentaro MaedaDepartment of Neurology, Nagoya University Graduate School of Medicine, Showa-ku, Nagoya, Aichi, Japan.
Yohei IguchiDepartment of Neurology, Nagoya University Graduate School of Medicine, Showa-ku, Nagoya, Aichi, Japan.
Jiayi LiDepartment of Neurology, Nagoya University Graduate School of Medicine, Showa-ku, Nagoya, Aichi, Japan.
Yosuke OguraDepartment of Neurology, Nagoya University Graduate School of Medicine, Showa-ku, Nagoya, Aichi, Japan.
Masaki IizukaDepartment of Neurology, Nagoya University Graduate School of Medicine, Showa-ku, Nagoya, Aichi, Japan.
Tomohiro AkashiCenter for 5D Cell Dynamics.
Kunihiko HinoharaCenter for 5D Cell Dynamics.
Shouta SugioDepartment of Anatomy and Molecular Cell Biology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan.
Hiroaki WakeDepartment of Anatomy and Molecular Cell Biology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan.
Masahiro NakatochiPublic Health Informatics Unit, Department of Integrated Health Sciences, and.
Masahisa KatsunoDepartment of Neurology, Nagoya University Graduate School of Medicine, Showa-ku, Nagoya, Aichi, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spinal and bulbar muscular atrophy (SBMA) is a neuromuscular disease caused by an expanded CAG repeat in the androgen receptor (AR) gene. To elucidate the cell type-specific temporal gene expression in SBMA, we performed single-nucleus RNA sequencing on the spinal cords of an SBMA mouse model (AR-97Q). Among all cell types, oligodendrocytes had the highest number of differentially expressed genes before disease onset. Analysis of oligodendrocyte clusters suggested that pathways associated with cation channels and synaptic function were activated before disease onset, with increased output from oligodendrocytes to neurons in AR-97Q mice compared with wild-type mice. These changes in the early stages were abrogated at the advanced stages. An oligodendrocyte model of SBMA showed phenotypes similar to those of AR-97Q mice at early stages, such as increased transcriptional changes in synapse organization, and Ca2+ imaging of oligodendrocytes in AR-97Q mice revealed the increased Ca2+ responses. A coculture system of primary rat oligodendrocytes and neurons revealed that the mutant AR in oligodendrocytes affected the activity and synchronization of neurons. These findings suggest that dysregulated cell-to-cell communication plays a critical role in early SBMA pathology and that synaptic or ion channel-related proteins, such as contactin associated protein 2 (Cntnap2) and NALCN channel auxiliary factor 1 (Fam155a), are potential therapeutic targets for SBMA.

Indexed as

OligodendrogliaSynapsesAnimalsDisease Models, AnimalGene Expression RegulationMaleMiceNeuronsRatsReceptors, AndrogenSpinal CordReceptors, AndrogenCell biologyIon channelsMolecular biologyNeuromuscular diseaseNeuroscience

Identifiers

PMID40548375
PMCPMC12220948

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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.