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巨噬细胞极化、代谢重编程及其在缺血性心脏病中的炎症作用。

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

机构信息

College of Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China.

Beijing Key Laboratory of Traditional Chinese Medicine (TCM) Syndrome and Formula, Beijing University of Chinese Medicine, Beijing, China.

出版信息

Front Immunol. 2022 Jul 18;13:934040. doi: 10.3389/fimmu.2022.934040. eCollection 2022.

Abstract

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.

摘要

巨噬细胞是一种具有高度可塑性的细胞,其极化激活作用代表了它们的功能焦点,与代谢重编程密切相关。巨噬细胞的代谢重编程表现为能量利用的偏向性,通过改变其能量利用方式来改变其炎症表型。代谢重编程效应与炎症作用的生物学过程相互作用,是巨噬细胞炎症功能的关键。在缺血性心脏病中,循环募集和组织驻留巨噬细胞的表型极化和代谢转变会影响心脏炎症效应的平衡,并决定疾病的消退和预后。在这篇综述中,我们提出了巨噬细胞极化和代谢重编程之间的内在联系,讨论了调节缺血性心脏病炎症效应中巨噬细胞的因素。我们的目的是建立可靠的调控途径,以便更好地靶向巨噬细胞代谢重编程过程,改善缺血性心脏病的症状。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcf8/9339672/3229573516c3/fimmu-13-934040-g001.jpg

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