Evidence map›Paper›PMID 40437654›Full record

ArticleThe FEBS journal2025

Cadherin-6 controls neuronal migration during mouse neocortical development via an integrin-mediated pathway.

Yuki Hirota, Rikaho Saito, Takao Honda, Hitomi Sano, Mayuko Hotta, Yukiko U Inoue, Takayoshi Inoue, Kazunori Nakajima

Abstract read
In one paragraph

Article in The FEBS journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Yuki HirotaDepartment of Anatomy, Keio University School of Medicine, Tokyo, Japan.ORCID https://orcid.org/0000-0001-9629-0038
Rikaho SaitoDepartment of Anatomy, Keio University School of Medicine, Tokyo, Japan.
Takao HondaDepartment of Anatomy, Keio University School of Medicine, Tokyo, Japan.
Hitomi SanoDepartment of Anatomy, Keio University School of Medicine, Tokyo, Japan.
Mayuko HottaDepartment of Biochemistry and Cellular Biology, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan.
Yukiko U InoueDepartment of Biochemistry and Cellular Biology, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan.ORCID https://orcid.org/0000-0002-4105-9127
Takayoshi InoueDepartment of Biochemistry and Cellular Biology, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan.ORCID https://orcid.org/0000-0001-7155-2150
Kazunori NakajimaDepartment of Anatomy, Keio University School of Medicine, Tokyo, Japan.ORCID https://orcid.org/0000-0003-1864-9425

Funding

Asahi Glass FoundationJapan Society for the Promotion of Science JP20H05688Japan Society for the Promotion of Science JP20K06670Japan Society for the Promotion of Science JP21K06413Japan Society for the Promotion of Science JP23H02491Japan Society for the Promotion of Science JP24H01972Japan Society for the Promotion of Science JP24K09668Japan Society for the Promotion of Science JP25K02437Keio Gijuku Academic Development FundsKeio Gijuku Fukuzawa Memorial Fund for the Advancement of Education and ResearchTakeda Science Foundation
6 · The paper itself

Abstract

During neocortical development, neuronal migration is highly regulated by multiple signaling cascades, including the cell adhesion molecules. Cadherin-6 (CDH6), an unusual cadherin molecule containing an RGD integrin-binding motif, has multiple functions in the developing nervous system, but whether it contributes to neuronal migration and positioning during neocortical development remains unknown. Here, we investigated the role of CDH6 in the developing cerebral cortex. Cdh6 knockdown (KD) using in utero electroporation revealed that CDH6 inhibition caused impaired radial migration and abnormal positioning of neurons. Time-lapse imaging analysis revealed that CDH6 is important for proper neuronal motility. Mechanistically, we show that CDH6 promotes the activation of integrin β1 on migrating neurons. The defect in neuronal migration caused by Cdh6 KD was rescued by moderate overexpression of integrin β1 and a KD-resistant form of wild-type CDH6, but not by CDH6 with a mutated RGD motif. These results suggest that CDH6 is required for cortical excitatory neurons to migrate radially by controlling integrin-mediated cell motility.

Indexed as

CadherinsCell MovementIntegrin beta1NeocortexNeuronsAnimalsGene Expression Regulation, DevelopmentalMiceSignal TransductionCadherinsIntegrin beta1Itgb1 protein, mousecadherin‐6integrinmigrationneocortical developmentneuron

Identifiers

PMID40437654
PMCPMC12524979

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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.