Macrophage Polarization, Metabolic Reprogramming, and Inflammatory Effects in Ischemic Heart Disease

被引:24
|
作者
Sun, Xiaoqian [1 ]
Li, Yanqin [1 ]
Deng, Qiong [1 ]
Hu, Yueyao [1 ]
Dong, Jianteng [1 ]
Wang, Wei [1 ,2 ,3 ]
Wang, Yong [1 ,2 ,4 ]
Li, Chun [2 ,5 ]
机构
[1] Beijing Univ Chinese Med, Coll Chinese Med, Beijing, Peoples R China
[2] Beijing Univ Chinese Med, Beijing Key Lab Tradit Chinese Med TCM Syndrome &, Beijing, Peoples R China
[3] Guangzhou Univ Chinese Med, Guangzhou, Peoples R China
[4] Beijing Univ Chinese Med, Sch Life Sci, Beijing, Peoples R China
[5] Beijing Univ Chinese Med, Modern Res Ctr Tradit Chinese Med TCM, Beijing, Peoples R China
来源
FRONTIERS IN IMMUNOLOGY | 2022年 / 13卷
基金
中国国家自然科学基金;
关键词
macrophage; polarization; metabolic reprogramming; inflammation; ischemic heart disease; OXIDATIVE-METABOLISM; ACTIVATION; IMMUNOMETABOLISM; MEDIATORS; GAMMA;
D O I
10.3389/fimmu.2022.934040
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Macrophages are highly plastic cells, and the polarization-activating actions that represent their functional focus are closely related to metabolic reprogramming. The metabolic reprogramming of macrophages manifests itself as a bias toward energy utilization, transforming their inflammatory phenotype by changing how they use energy. Metabolic reprogramming effects crosstalk with the biological processes of inflammatory action and are key to the inflammatory function of macrophages. In ischemic heart disease, phenotypic polarization and metabolic shifts in circulating recruitment and tissue-resident macrophages can influence the balance of inflammatory effects in the heart and determine disease regression and prognosis. In this review, we present the intrinsic link between macrophage polarization and metabolic reprogramming, discussing the factors that regulate macrophages in the inflammatory effects of ischemic heart disease. Our aim is to estabilsh reliable regulatory pathways that will allow us to better target the macrophage metabolic reprogramming process and improve the symptoms of ischemic heart disease.
引用
收藏
页数:7
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