Serum-Derived Exosomal TBX2-AS1 Exacerbates COPD by Altering the M1/M2 Ratio of Macrophages through Regulating the miR-423-5p/miR-23b-3p Axis

被引:0
|
作者
Wang, Jinhai [1 ]
Luo, Qing [2 ]
Gu, Tijun [1 ]
An, Fenqin [3 ]
Zhou, Yunzheng [3 ]
Min, Yeping [1 ]
Zhang, Ruiren [3 ]
Jiang, Yiming [1 ,3 ]
机构
[1] Nanjing Med Univ, Affiliated Changzhou Peoples Hosp 2, Dept Emergency, Changzhou 213003, Peoples R China
[2] Peoples Hosp Hainan Tibetan Autonomous Prefecture, Dept Internal Med, Qinghai, Hainan Tibetan, Peoples R China
[3] Peoples Hosp Hainan Tibetan Autonomous Prefecture, Dept Emergency, Qinghai, Hainan Tibetan, Peoples R China
关键词
COPD; macrophage polarization; miR-423-5p/miR-23b-3p; serum exosomes; TBX2-AS1; OBSTRUCTIVE PULMONARY-DISEASE; INFLAMMATION;
D O I
10.1080/08820139.2024.2434692
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
ObjectiveTo investigate the mechanism of serum exosomes in chronic obstructive pulmonary disease (COPD), especially the effect of lncRNA TBX2-AS1 on macrophage polarization.MethodsScreen differentially expressed genes through bioinformatics analysis, detect the expression of related molecules in clinical samples and cell experiments, construct a mouse model and conduct functional rescue experiments, using various experimental techniques such as RT - qPCR, Western Blot, flow cytometry, ELISA, and luciferase reporter assay.ResultsTBX2-AS1 is highly expressed in the serum and serum exosomes of COPD patients, and it can promote macrophage M1 polarization and inhibit M2 polarization; it exerts its role by negatively regulating the miR-423-5p/miR-23b - 3p axis, where miR-423-5p inhibits CELSR2 expression to prevent M1 polarization, and miR-23b-3p inhibits NEK6 expression to promote M2 polarization; in vivo experiments, down-regulation of CELSR2/NEK6 can reverse the promoting effect of COPD serum exosomes on lung injury and inflammation.ConclusionCOPD serum exosomes deliver TBX2-AS1 to macrophages, regulate the miR-423-5p-CELSR2/miR-23b-3p-NEK6 pathway, affect macrophage polarization, and exacerbate the progression of COPD, providing new directions and potential targets for the diagnosis and treatment of COPD.
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页码:271 / 295
页数:25
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