Evidence map›Paper›PMID 40926092›Full record

ArticleMolecular psychiatry2026

Semaphorin 3A-mediated perineuronal nets formation incubates depressive-like behaviors in male mice via activating parvalbumin-expressing interneurons.

Yuan-Xi Mei, Hong-Sheng Chen, Qun-Ling Cao, Wan-Wan Lv, Yang Liu, Si-Long Deng, Qigang Zhou, Zhang-Jin Zhang, Fang Wang, Zhuang-Li Hu and 1 more

Abstract read
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In one paragraph

Article in Molecular psychiatry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Developmental CA2 perineuronal net reduction restores social memory inbioRxiv : the preprint server for biology · 2025
    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

11 authors.

Yuan-Xi Mei *Department of Pharmacology, School of Basic Medicine and Department of Pharmacy, Tongji Hospital, Tongji Medical College; and State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Diseases, Huazhong University of Science and Technology, Wuhan, Hubei, 430030, China.ORCID http://orcid.org/0009-0003-4691-0747
Hong-Sheng Chen *Department of Pharmacology, School of Basic Medicine and Department of Pharmacy, Tongji Hospital, Tongji Medical College; and State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Diseases, Huazhong University of Science and Technology, Wuhan, Hubei, 430030, China.
Qun-Ling CaoDepartment of Pharmacology, School of Basic Medicine and Department of Pharmacy, Tongji Hospital, Tongji Medical College; and State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Diseases, Huazhong University of Science and Technology, Wuhan, Hubei, 430030, China.
Wan-Wan LvDepartment of Pharmacology, School of Basic Medicine and Department of Pharmacy, Tongji Hospital, Tongji Medical College; and State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Diseases, Huazhong University of Science and Technology, Wuhan, Hubei, 430030, China.
Yang LiuDepartment of Pharmacology, School of Basic Medicine and Department of Pharmacy, Tongji Hospital, Tongji Medical College; and State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Diseases, Huazhong University of Science and Technology, Wuhan, Hubei, 430030, China.
Si-Long DengDepartment of Pharmacology, School of Basic Medicine and Department of Pharmacy, Tongji Hospital, Tongji Medical College; and State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Diseases, Huazhong University of Science and Technology, Wuhan, Hubei, 430030, China.
Qigang ZhouDepartment of Clinical Pharmacology, School of Pharmacy and The Key Center of Gene Technology Drugs of Jiangsu Province, Nanjing Medical University, Nanjing, 211166, China.ORCID http://orcid.org/0000-0003-3870-3070
Zhang-Jin ZhangSchool of Chinese Medicine, The University of Hong Kong, Hong Kong SAR, China.ORCID http://orcid.org/0000-0002-8416-3426
Fang WangDepartment of Pharmacology, School of Basic Medicine and Department of Pharmacy, Tongji Hospital, Tongji Medical College; and State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Diseases, Huazhong University of Science and Technology, Wuhan, Hubei, 430030, China. wangfanghust@hust.edu.cn.ORCID http://orcid.org/0000-0002-4781-8673
Zhuang-Li HuDepartment of Pharmacology, School of Basic Medicine and Department of Pharmacy, Tongji Hospital, Tongji Medical College; and State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Diseases, Huazhong University of Science and Technology, Wuhan, Hubei, 430030, China. zlhu916@hust.edu.cn.ORCID http://orcid.org/0000-0002-6683-9744
Jian-Guo ChenDepartment of Pharmacology, School of Basic Medicine and Department of Pharmacy, Tongji Hospital, Tongji Medical College; and State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Diseases, Huazhong University of Science and Technology, Wuhan, Hubei, 430030, China. chenjg@hust.edu.cn.ORCID http://orcid.org/0000-0002-7805-3589

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82130110 and 82341063 to JGCNational Natural Science Foundation of China (National Science Foundation of China) 82201654National Natural Science Foundation of China (National Science Foundation of China) 82204371National Natural Science Foundation of China (National Science Foundation of China) 82273912National Natural Science Foundation of China (National Science Foundation of China) U21A20363
6 · The paper itself

Abstract

Dysfunction of parvalbumin-expressing interneurons (PV-INs) in the cerebral cortex has been implicated in major depressive disorder. Perineuronal nets (PNNs), which encapsulate PV-INs, are considered to influence the structural and functional properties of PV-INs. Semaphorin 3A (Sema3A) is a secreted protein constituent of PNNs, but the specific roles of Sema3A in modulating PV-INs during stress remain unknown. Here, we demonstrated that Sema3A, secreted by GABAergic interneurons, contributed to the response to chronic stress in male mice. The accumulation of Sema3A interacts with PNNs and facilitates PNNs wrapping of PV-INs, leading to a decrease in inhibitory synaptic input and an increase in the excitability of PV-INs. Sema3A-mediated formation of PNNs and the subsequent increase in PV-INs excitability may promote the development of depressive-like behaviors induced by stress. These results elucidate a molecular pathway in which Sema3A, a component of PNNs, dynamically governs the function of PV-INs to facilitate adaptive behavioral responses to stress.

Indexed as

DepressionInterneuronsSemaphorin-3AAnimalsBehavior, AnimalCerebral CortexDisease Models, AnimalExtracellular MatrixGABAergic NeuronsMajor Depressive DisorderMaleMiceMice, Inbred C57BLNerve NetParvalbuminsStress, PsychologicalParvalbuminsSema3a protein, mouseSemaphorin-3A

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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.