Evidence map›Paper›PMID 40846958›Full record

ArticleMolecular brain2025

Comprehensive behavioral phenotyping of male Septin 3-deficient mice reveals task-specific abnormalities.

Natsumi Ageta-Ishihara, Keizo Takao, Tsuyoshi Miyakawa, Makoto Kinoshita

Abstract read
In one paragraph

Article in Molecular brain, 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

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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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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

4 authors.

Natsumi Ageta-IshiharaDepartment of Biomolecular Science, Faculty of Science, Toho University, 2-2-1 Miyama, Funabashi, 274-8510, Chiba, Japan. natsumi.ageta-ishihara@sci.toho-u.ac.jp.
Keizo TakaoDepartment of Behavioral Physiology, Faculty of Medicine, University of Toyama, Toyama, 930-0194, Japan.
Tsuyoshi MiyakawaDivision of Systems Medical Science, Center for Medical Science, Fujita Health University, Toyoake, Aichi, 470-1192, Japan.
Makoto KinoshitaDepartment of Molecular Biology, Division of Biological Sciences, Nagoya University Graduate School of Science, Chikusa-ku, Nagoya, 464-8602, Japan. kinoshita.makoto.u4@f.mail.nagoya-u.ac.jp.

Funding

Kaken Pharmaceutical,Japan 221S0003, 23370084, 24770184, 23K06394
6 · The paper itself

Abstract

The septin cytoskeleton is recognized as the fourth component of the cytoskeleton. Septin 3 (SEPT3)/G-septin is a neuron-selective subunit of the septin family and is widely expressed in mature neurons. We previously demonstrated that SEPT3 regulates long-term potentiation (L-LTP)-dependent extension of smooth endoplasmic reticulum (sER) into dendritic spines of granule cells in the hippocampal dentate gyrus (DG), and that Sept3 knockout (Sept3−/−) mice exhibited impairments in DG-dependent spatial long-term memory. However, the broader behavioral consequences of SEPT3 deficiency remain largely unexplored. To address this, we conducted comprehensive behavioral phenotyping of male Sept3−/− mice using a standardized test battery. In the social interaction test in a novel environment, Sept3−/− mice showed increased contact frequency and interaction time. In contrast, performance in the three-chamber social interaction test was comparable to wild-type mice, indicating context-dependent deficits. In contextual fear conditioning, Sept3−/− mice displayed reduced freezing 24 h after training, but not 35 days later. In the T-maze forced alternation task, deficits were observed in choice accuracy and latency. These results demonstrate that Sept3−/− mice exhibit selective behavioral impairments depending on task demands and environmental context. Our findings provide the first behavioral characterization of Sept3−/− mice and offer new insights into the functional role of SEPT3, laying a foundation for future investigation into its molecular and circuit-level mechanisms.

Indexed as

Behavior, AnimalSeptinsAnimalsFearMaleMaze LearningMice, Inbred C57BLMice, KnockoutPhenotypeSocial InteractionSeptinsBehavioral phenotypingContextual fear conditioningKnockout miceSeptinSocial interactionSpatial working memory

Identifiers

PMID40846958
PMCPMC12374300

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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.