Evidence map›Paper›PMID 37771931›Full record

ArticleFrontiers in cellular neuroscience2023

Replenished microglia partially rescue schizophrenia-related stress response.

Ling Yan, Fang-Ling Xuan, Song Chen, Mengzhuang Gou, Wenjin Chen, Yanli Li, Zhiren Wang, Leilei Wang, Ting Xie, Fengmei Fan and 3 more

Abstract read
In one paragraph

Article in Frontiers in cellular neuroscience, 2023. 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

13 authors.

Ling YanInstitute of Biomedicine and Translational Medicine, Faculty of Medicine, University of Tartu, Tartu, Estonia.
Fang-Ling XuanInstitute of Biomedicine and Translational Medicine, Faculty of Medicine, University of Tartu, Tartu, Estonia.
Song ChenPsychiatry Research Centre, Beijing Huilongguan Hospital, Peking University Health Science Center, Beijing, China.
Mengzhuang GouPsychiatry Research Centre, Beijing Huilongguan Hospital, Peking University Health Science Center, Beijing, China.
Wenjin ChenPsychiatry Research Centre, Beijing Huilongguan Hospital, Peking University Health Science Center, Beijing, China.
Yanli LiPsychiatry Research Centre, Beijing Huilongguan Hospital, Peking University Health Science Center, Beijing, China.
Zhiren WangPsychiatry Research Centre, Beijing Huilongguan Hospital, Peking University Health Science Center, Beijing, China.
Leilei WangPsychiatry Research Centre, Beijing Huilongguan Hospital, Peking University Health Science Center, Beijing, China.
Ting XiePsychiatry Research Centre, Beijing Huilongguan Hospital, Peking University Health Science Center, Beijing, China.
Fengmei FanPsychiatry Research Centre, Beijing Huilongguan Hospital, Peking University Health Science Center, Beijing, China.
Alexander ZharkovskyInstitute of Biomedicine and Translational Medicine, Faculty of Medicine, University of Tartu, Tartu, Estonia.
Yunlong TanPsychiatry Research Centre, Beijing Huilongguan Hospital, Peking University Health Science Center, Beijing, China.
Li TianInstitute of Biomedicine and Translational Medicine, Faculty of Medicine, University of Tartu, Tartu, Estonia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Microglia play an important role in the maintenance of brain and behavioral homeostasis. The protective effect of microglial replenishment was reported in neurological diseases, but whether microglial therapy would benefit psychiatric disorders such as schizophrenia has been unclear. As schizophrenia is a stress-vulnerable disorder and psychosocial stress promotes inflammation and microglial activation, we aim to understand how microglial replenishment works in stress-associated schizophrenia. Methods: We used a CSF1R-mediated pharmacological approach to study repopulated microglia (repMg) in a cohort of mice ( Results: Reborn microglia attenuated CUS-induced learned hopelessness and social withdrawal but not anxiety in mice. Compared to control, CUS- or repMg-induced differentially expressed genes (DEGs) in the prefrontal cortex regulated nervous system development and axonal guidance. CUS also caused microglial hyper-ramification and increased engulfment of synaptophysin and vesicular glutamate transporter-2 by microglia and astrocytes, which were recovered in CUS + repMg (all Conclusion: Microglial replenishment may potentially benefit psychiatric disorders such as schizophrenia.

Indexed as

chronic unpredictable stresshippocampusmicroglial replenishmentprefrontal cortexschizophreniasynaptic pruning

Identifiers

PMID37771931
PMCPMC10522857

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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.