Evidence map›Paper›PMID 42265101›Full record

ArticleNature communications2026

Scg2 drives corticospinal circuit reorganization with spinal premotor interneurons and astrocytes for motor recovery after stroke in mice.

Tokiharu Sato, Yuka Nakamura, Kana Hoshina, Ken-Ichi Inoue, Masahiko Takada, Masato Yano, Hitoshi Matsuzawa, Masaki Ueno

Abstract read
In one paragraph

Article in Nature communications, 2026. 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. Review
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

8 authors.

Tokiharu SatoDepartment of System Pathology for Neurological Disorders, Brain Research Institute, Niigata University, Niigata, Niigata, Japan.ORCID 0009-0007-8280-7332
Yuka NakamuraDepartment of System Pathology for Neurological Disorders, Brain Research Institute, Niigata University, Niigata, Niigata, Japan.ORCID 0009-0003-2188-0641
Kana HoshinaDepartment of System Pathology for Neurological Disorders, Brain Research Institute, Niigata University, Niigata, Niigata, Japan.
Ken-Ichi InoueInstitute for the Evolutionary Origins of Human Behavior, Kyoto University, Inuyama, Aichi, Japan.ORCID 0000-0002-5683-5280
Masahiko TakadaInstitute for the Evolutionary Origins of Human Behavior, Kyoto University, Inuyama, Aichi, Japan.ORCID 0000-0003-0774-2333
Masato YanoDivision of Neurobiology and Anatomy, Graduate School of Medical and Dental Sciences, Niigata University, Niigata, Niigata, Japan.ORCID 0000-0003-0589-478X
Hitoshi MatsuzawaCenter for Integrated Human Brain Science, Niigata University, Niigata, Niigata, Japan.
Masaki UenoDepartment of System Pathology for Neurological Disorders, Brain Research Institute, Niigata University, Niigata, Niigata, Japan. ms-ueno@bri.niigata-u.ac.jp.ORCID 0000-0003-1484-9921

Funding

Japan Agency for Medical Research and Development (AMED) JP21gm1210005, JP21zf0127004Kato Memorial Bioscience Foundation N/ATakeda Science Foundation N/ATokyo Biochemical Research Foundation (TBRF) N/A
6 · The paper itself

Abstract

Brain injuries such as stroke damage neural circuitry and lead to functional deficits. Spared motor pathways are often reorganized for recovery; however, the connectivity and mechanisms that drive the reorganization are largely unknown. Here, we demonstrate structural and functional connectivity reformed by corticospinal axons after stroke in male mice and determine a secretory protein that drives the reorganization. We first find that corticospinal axons innervate the denervated cervical cord and reconnect to premotor V2a interneurons after stroke. Kinematic analyses and chemogenetic silencing reveal their contribution to motor recovery. Translated mRNA expression analyses identify a secretory protein secretogranin II (Scg2), which is upregulated in astrocytes by injury-induced ATP and in V2a neurons by rehabilitation-induced neural activity. Scg2 promotes axon growth via cAMP and S6 and enhances axon rewiring, while its knockdown attenuates it. Our data reveal the neural substrate and molecular mechanism to induce reorganization and recovery, providing therapeutic targets for central nervous system (CNS) injuries.

Indexed as

AstrocytesInterneuronsPyramidal TractsRecovery of FunctionStrokeAnimalsAxonsMaleMiceMice, Inbred C57BLSpinal Cord

Identifiers

PMID42265101
PMCPMC13249867

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.