Evidence map›Paper›PMID 41854227›Full record

ArticleThe Journal of comparative neurology2026

Localization of Puncta Adherentia Junctions at GABAergic Synapses on Parvalbumin-Positive GABAergic Inhibitory Neurons in the Mouse Hippocampus.

Kimitaka Katanazaka, Hajime Shiotani, Muneaki Miyata, Takeshi Kameyama, Shin Kedashiro, Ryouhei Komaki, Shota Nishii, Yutaro Kashiwagi, Yuka Sato, Shigeo Okabe and 4 more

Abstract read
In one paragraph

Article in The Journal of comparative neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

14 authors.

Kimitaka KatanazakaDivision of Pathogenetic Signaling, Department of Psychiatry, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.
Hajime ShiotaniDivision of Pathogenetic Signaling, Department of Psychiatry, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.
Muneaki MiyataDivision of Pathogenetic Signaling, Department of Psychiatry, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.
Takeshi KameyamaDivision of Pathogenetic Signaling, Department of Psychiatry, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.
Shin KedashiroDivision of Pathogenetic Signaling, Department of Psychiatry, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.
Ryouhei KomakiDivision of Pathogenetic Signaling, Department of Psychiatry, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.
Shota NishiiDivision of Pathogenetic Signaling, Department of Psychiatry, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.
Yutaro KashiwagiDepartment of Cellular Neurology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Yuka SatoDepartment of Cellular Neurology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Shigeo OkabeDepartment of Cellular Neurology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Norio ChiharaDivision of Neurology, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.
Riki MatsumotoDivision of Neurology, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.ORCID https://orcid.org/0000-0003-3985-9210
Kiyohito MizutaniDivision of Pathogenetic Signaling, Department of Psychiatry, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.ORCID https://orcid.org/0000-0003-1758-8026
Yoshimi TakaiDivision of Pathogenetic Signaling, Department of Psychiatry, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.

Funding

Japan Agency for Medical Research and Development JP22gm1710005Japan Science and Technology Agency JPMJMS2024Japan Science and Technology Agency JPMJPF2018Japan Society for the Promotion of Science JP20H05895Japan Society for the Promotion of Science JP21K06410Japan Society for the Promotion of Science JP22K15213Japan Society for the Promotion of Science JP22KJ2273Japan Society for the Promotion of Science JP24K18228Ministry of Education, Culture, Sports, Science and Technology
6 · The paper itself

Abstract

Puncta adherentia junctions (PAJs) have been observed at glutamatergic excitatory synapses on glutamatergic excitatory neurons (E→E synapses) in the mouse hippocampus and are considered to be the mechanical adhesion sites between axon terminals and dendritic shafts. However, it remains unclear whether they are present at other types of synapses, such as glutamatergic synapses on GABAergic inhibitory neurons (E→I synapses) and GABAergic synapses on excitatory neurons (I→E synapses) and inhibitory neurons (I→I synapses). We showed here that the PAJ components, such as nectin-1, nectin-3, l-afadin, N-cadherin, β-catenin, and αN-catenin, were observed at all four types of synapses in cultured mouse hippocampal neurons. In the adult mouse hippocampus, these PAJ components were observed at a subset of I→I synapses on parvalbumin-positive GABAergic inhibitory neurons, similarly to their presence at E→E synapses in the CA1 and CA3 regions. In contrast, several PAJ components, including nectin-3, l-afadin, N-cadherin, β-catenin, and αN-catenin, were observed at E→I and I→E synapses, whereas nectin-1 was absent. These results indicate that the PAJs are formed at a subset of I→I synapses in addition to E→E synapses, where all examined PAJ components are present, whereas E→I and I→E synapses exhibit only partial localization of these components, reflecting molecular diversity among different synapses in the adult mouse hippocampus.

Indexed as

GABAergic NeuronsHippocampusParvalbuminsSynapsesAnimalsbeta CateninCadherinsCell Adhesion MoleculesCells, CulturedMaleMiceMice, Inbred C57BLMicrofilament ProteinsNectinsNeural Inhibitionafadinbeta CateninCadherinsCell Adhesion MoleculesMicrofilament ProteinsNectin1 protein, mouseNectin3 protein, mouseNectinsParvalbuminsafadincateninGABAergic synapsesglutamatergic synapsesN‐cadherinnectinpuncta adherentia junctions (PAJs)

Identifiers

PMID41854227
PMCPMC13045645

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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.