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首页|期刊导航|神经损伤与功能重建|血小板因子4通过Trem2调控AD细胞模型中小胶质细胞极化促进Aβ清除的研究

血小板因子4通过Trem2调控AD细胞模型中小胶质细胞极化促进Aβ清除的研究

僧茜茜 李敏 宋晨冉 叶城辰 王雨晨 黄胜杰 成勇

神经损伤与功能重建2026,Vol.21Issue(3):125-130,6.
神经损伤与功能重建2026,Vol.21Issue(3):125-130,6.DOI:10.16780/j.cnki.sjssgncj.20251364

血小板因子4通过Trem2调控AD细胞模型中小胶质细胞极化促进Aβ清除的研究

Platelet Factor 4 Promotes Amyloid-β Clearance through Regulating Microglia Polarization via Trem2 in AD Cell Models

僧茜茜 1李敏 2宋晨冉 2叶城辰 3王雨晨 1黄胜杰 1成勇4

作者信息

  • 1. 武汉科技大学医学部医学院 武汉 430065||中部战区总医院 神经内科 武汉 430070
  • 2. 中部战区总医院 基础医学实验室 武汉 430070||湖北省中枢神经系统肿瘤发生与干预重点实验室 武汉 430070
  • 3. 武汉科技大学医学部医学院 武汉 430065||中部战区总医院 基础医学实验室 武汉 430070
  • 4. 中部战区总医院 神经内科 武汉 430070
  • 折叠

摘要

Abstract

Objective:To investigate the potential impact of platelet factor 4(PF4)on the M1/M2 polarization of microglia in an Alzheimer's disease(AD)cell model and its possible molecular mechanisms.Methods:An AD cell model was induced by treating BV2 microglial cells with A β 1-42,followed by PF4 intervention.Furthermore,Trem2 expression was knocked down in BV2 cells through Trem2-siRNA transfection.Cell viability was assessed using the CCK8 assay;levels of TNF-α,IL-6,and IL-1 β were measured by ELISA;the expressions of Trem2,iNOS,and Arg1 were detected via double-label immunofluorescence and Western blot analyses;mRNA levels of Trem2,iNOS,Arg1,TNF-α,and IL-10 were determined by RT-qPCR;and phagocytic function was evaluated using flow cytometry.Results:Compared with the control group,the A β 1-42 group exhibited significantly elevated expression levels of M1 phenotype markers(iNOS,TNF-α,IL-1 β)and IL-6,along with markedly decreased expression of M2 phenotype markers(Arg1,IL-10)and Trem2.In contrast,the(Aβ1-42+PF4)group showed reduced expression of M1 phenotype markers(iNOS,TNF-α,IL-1β)and IL-6,increased expression of M2 phenotype markers(Arg1,IL-10)and Trem2,and enhanced phagocytic capacity for A β 1-42 compared with the Aβ1-42 group.However,compared with the(Trem2-siRNA+Aβ1-42)group,PF4 failed to exert the aforementioned effects in BV2 cells in the(Trem2-siRNA+Aβ1-42+PF4)group.Conclusion:PF4 can regulate microglial polarization via Trem2,alleviate AD-related neuroinflammation,and promote the clearance of Aβ1-42.

关键词

小胶质细胞极化/血小板因子4/阿尔茨海默病/髓样细胞触发受体2

Key words

microglial polarization/platelet factor 4/Alzheimer's disease/triggering receptor expressed on myeloid cells-2

分类

医药卫生

引用本文复制引用

僧茜茜,李敏,宋晨冉,叶城辰,王雨晨,黄胜杰,成勇..血小板因子4通过Trem2调控AD细胞模型中小胶质细胞极化促进Aβ清除的研究[J].神经损伤与功能重建,2026,21(3):125-130,6.

基金项目

湖北省卫生健康科技项目(溶酶体脂质代谢调控铁死亡在阿尔茨海默病的作用与机制研究,No.WJ2025Q085) (溶酶体脂质代谢调控铁死亡在阿尔茨海默病的作用与机制研究,No.WJ2025Q085)

神经损伤与功能重建

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