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Navigating the Complex Terrain of Dysregulated Microglial Function in Depressive Disorders: Insights, Challenges and Future Directions.

作者信息

Zhang Yuling, Tang Chaozhi

出版信息

Aging Dis. 2024 Mar 26;16(2):1023-1035. doi: 10.14336/AD.2024.0326.


DOI:10.14336/AD.2024.0326
PMID:38607738
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11964431/
Abstract

Microglia are crucial immune cells found in the central nervous system. Multiple investigations have substantiated the correlation between the development of depression and neuroinflammation resulting from impaired microglial activity. Through extensive research on the phenotype, function, imaging technology, multi-omics analysis, and in vitro culture of microglia in depressive disorder, the understanding of the relationship between microglia and depression has become more intricate. Various therapeutic approaches have been suggested, but a thorough analysis of the obstacles to clinical application has not been conducted. This paper explores the innovative advancement of microglia detection technology, recent research findings on microglia identification and epigenetic modification, the variability of microglia in different conditions, the relationship between microglia dysfunction and the onset of depression, the progress and challenges of microglia-targeted therapy for depression, and the current obstacles and future prospects in studying dysregulated microglial function in depressive disorders.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e64/11964431/e609466228a0/AD-16-2-1023-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e64/11964431/0698ee6b037b/AD-16-2-1023-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e64/11964431/e609466228a0/AD-16-2-1023-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e64/11964431/0698ee6b037b/AD-16-2-1023-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e64/11964431/e609466228a0/AD-16-2-1023-g2.jpg

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引用本文的文献

[1]
The central role of microglia in major depressive disorder and its potential as a therapeutic target.

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[2]
Magnolol Ameliorates Depression Through Modulating the TREM2-DOK3-ERK Pathway.

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本文引用的文献

[1]
CircDYM attenuates microglial apoptosis via CEBPB/ZC3H4 axis in LPS-induced mouse model of depression.

Int J Biol Macromol. 2024-1

[2]
iPS-cell-derived microglia promote brain organoid maturation via cholesterol transfer.

Nature. 2023-11

[3]
The role of the Toll like receptor 4 signaling in sex-specific persistency of depression-like behavior in response to chronic stress.

Brain Behav Immun. 2024-1

[4]
The role of CD38 in inflammation-induced depression-like behavior and the antidepressant effect of (R)-ketamine.

Brain Behav Immun. 2024-1

[5]
Chronic psychosocial stress triggers microglial-/macrophage-induced inflammatory responses leading to neuronal dysfunction and depressive-related behavior.

Glia. 2024-1

[6]
Development of a novel histone deacetylase inhibitor unveils the role of HDAC11 in alleviating depression by inhibition of microglial activation.

Biomed Pharmacother. 2023-10

[7]
Association of Single Nucleotide Polymorphisms of Cytokine Genes with Depression, Schizophrenia and Bipolar Disorder.

Genes (Basel). 2023-7-17

[8]
Integrating spatial and single-nucleus transcriptomic data elucidates microglial-specific responses in female cynomolgus macaques with depressive-like behaviors.

Nat Neurosci. 2023-8

[9]
Modified Xiaoyao San reverses lipopolysaccharide-induced depression-like behavior through suppressing microglia M1 polarization via enhancing autophagy involved in PI3K/Akt/mTOR pathway in mice.

J Ethnopharmacol. 2023-10-28

[10]
Analysis of the microglia transcriptome across the human lifespan using single cell RNA sequencing.

J Neuroinflammation. 2023-5-30

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