HMGB1 promotes LPS-induced M1 polarization and apoptosis in microglia by mediating the expression of immune and inflammation-related genes

HMGB1 may drive microglia toward a pro-inflammatory M1 phenotype, thereby mediating neuroinflammatory damage in POCD, potentially through activation of STAT, TNF, and IL-17 signaling pathways. Targeting HMGB1 and its downstream genes (e.g., Ccl22, Lcn2, Stat5a, Tlr2, Cd74, Egr2) could provide effective diagnostic and interventional strategies for POCD.

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Publication Details

Journal
Brain Research Bulletin
Published
2025-11-02
DOI
https://doi.org/10.1016/j.brainresbull.2025.111615
Citations
2
Primary Topic
Neuroinflammation and Neurodegeneration Mechanisms
Type
article
Field-Weighted Citation Impact
1.68
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article

HMGB1 promotes LPS-induced M1 polarization and apoptosis in microglia by mediating the expression of immune and inflammation-related genes

Fan Yang, Xiang Cui, Qi Huang, Na Li et al.
2 citations
Brain Research Bulletin
Neuroinflammation and Neurodegeneration Mechanisms
1.68
article

HMGB1 promotes LPS-induced M1 polarization and apoptosis in microglia by mediating the expression of immune and inflammation-related genes

Fan Yang, Xiang Cui, Qi Huang, Na Li, Li Zhao, Huiwen Zhang, Lin Ma, Wan‐Wan Lin, Ma HanXiang
article en
2 citations

Abstract

HMGB1 may drive microglia toward a pro-inflammatory M1 phenotype, thereby mediating neuroinflammatory damage in POCD, potentially through activation of STAT, TNF, and IL-17 signaling pathways. Targeting HMGB1 and its downstream genes (e.g., Ccl22, Lcn2, Stat5a, Tlr2, Cd74, Egr2) could provide effective diagnostic and interventional strategies for POCD.

Brain Research BulletinVol. 233
Ningxia Medical University (CN), Ningxia Medical University General Hospital (CN)
Openalex Percentile: Top 13%
Neuroinflammation and Neurodegeneration Mechanisms
1.68
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