Evidence map›Paper›PMID 40930803›Full record

ArticleJournal of anatomy2026

Laminin 332 regulates glial fibrillary acidic protein expression and astrocyte maturation during spinal cord development.

Tetsuto Yamaura, Mao Watanabe, Yusuke Minato, Rika Sakuma, Seishi Maeda, Toshiya Tachibana, Hideshi Yagi

Abstract read
In one paragraph

Article in Journal of anatomy, 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. 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

7 authors.

Tetsuto YamauraDepartment of Anatomy and Cell Biology, Hyogo Medical University School of Medicine, Nishinomiya, Hyogo, Japan.ORCID https://orcid.org/0000-0002-5934-4313
Mao WatanabeDepartment of Anatomy and Cell Biology, Hyogo Medical University School of Medicine, Nishinomiya, Hyogo, Japan.
Yusuke MinatoDepartment of Anatomy and Cell Biology, Hyogo Medical University School of Medicine, Nishinomiya, Hyogo, Japan.ORCID https://orcid.org/0000-0003-1678-6856
Rika SakumaDepartment of Anatomy and Cell Biology, Hyogo Medical University School of Medicine, Nishinomiya, Hyogo, Japan.ORCID https://orcid.org/0000-0002-4907-3046
Seishi MaedaDepartment of Anatomy and Cell Biology, Hyogo Medical University School of Medicine, Nishinomiya, Hyogo, Japan.ORCID https://orcid.org/0000-0001-9827-7785
Toshiya TachibanaDepartment of Orthopaedic Surgery, Hyogo Medical University School of Medicine, Nishinomiya, Hyogo, Japan.ORCID https://orcid.org/0000-0003-0714-0340
Hideshi YagiDepartment of Anatomy and Cell Biology, Hyogo Medical University School of Medicine, Nishinomiya, Hyogo, Japan.ORCID https://orcid.org/0000-0002-8506-8965

Funding

Hyogo Medical University Physician-Scientist Training Program
6 · The paper itself

Abstract

The white matter of the spinal cord is essential for sensory and motor signaling, and its proper development is crucial for establishing functional neuronal circuits. However, the mechanisms underlying white matter formation remain incompletely understood. We hypothesized that the extracellular matrix, particularly laminins, plays a key role in this process. The spatiotemporal expression patterns of laminins during spinal cord white matter development have not been fully characterized. Here, we examined the distribution and function of laminins during spinal cord development. Laminin 332 localized to the marginal zone of the spinal cord at embryonic days 12 (E12) and 14 (E14), coinciding with periods of extensive axonal growth. Immunohistochemical analysis revealed an increase in glial fibrillary acidic protein (GFAP)-positive fibers in laminin 332-enriched regions. Laminin 332 promoted GFAP expression in astrocyte precursor cells, an effect attenuated by integrin α6β4 blockade, suggesting that laminin 332 signals through integrins to support astrocyte maturation. Our findings indicate that laminin 332 not only serves as a structural component of the extracellular matrix but also actively regulates glial differentiation during spinal cord development. Understanding the signaling pathways mediated by laminin 332 may inform therapeutic strategies aimed at enhancing spinal cord regeneration by modulating astrocyte behavior and promoting axonal growth.

Indexed as

AstrocytesCell Adhesion MoleculesGlial Fibrillary Acidic ProteinSpinal CordAnimalsCell DifferentiationLamininCell Adhesion MoleculesGlial Fibrillary Acidic ProteinLamininastrocytesextracellular matrixneurodevelopmentprojection neuronswhite matter formation

Identifiers

PMID40930803
PMCPMC12881867

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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.