Zhu Minyan, Zhou Hongmei, Zhou Lei, Yang Yaping, Chen Rong
Department of Pharmacy, the First Affiliated Hospital of Soochow University, No.899, Pinghai Road, Gusu District, Suzhou, Suzhou, Jiangsu, China.
Department of Pharmacology, Soochow University, No.199, Ren'ai Road, Suzhou Industrial Park, Suzhou, Suzhou, Jiangsu, China.
J Cardiothorac Surg. 2025 Jul 18;20(1):307. doi: 10.1186/s13019-025-03541-4.
Cardiovascular diseases (CVD) are the leading causes of death worldwide, imposing a great burden on society. In recent years, macrophages have garnered widespread attention in CVD research. Macrophages are an important component of the body's immune system, playing a critical role in clearing pathogens, repairing damaged tissues, and regulating inflammatory responses, have the potential to serve as a potential target for the treatment of CVD.
To make up this review, studies covering Macrophage subtypes and signaling pathways, CVD were selected from the main medical databases.
In CVD, macrophages can differentiate into different phenotypes(M1, M2, M4, et al.) according to their microenvironment by their plasticity and heterogeneity, release different cytokines, are regulated by multiple signaling pathways(PI3K/Akt, TLR4, TGF-β/Smads, et al.), and play other functions in CVD. M1 initiates and maintains inflammation by secreting pro-inflammatory factors, and M2 participates in the regression of inflammation and tissue repair by secreting anti-inflammatory factors. Therefore, by regulating the signaling pathway, it reduces the aggregation of macrophages, promotes the polarization of macrophages to M2, or restores M1/M2 homeostasis to improve the inflammatory microenvironment and delay CVD progression.
心血管疾病(CVD)是全球主要的死亡原因,给社会带来了巨大负担。近年来,巨噬细胞在心血管疾病研究中受到广泛关注。巨噬细胞是人体免疫系统的重要组成部分,在清除病原体、修复受损组织和调节炎症反应中发挥关键作用,有可能成为治疗心血管疾病的潜在靶点。
为撰写本综述,从主要医学数据库中选取了涵盖巨噬细胞亚型和信号通路、心血管疾病的研究。
在心血管疾病中,巨噬细胞可根据其微环境,凭借其可塑性和异质性分化为不同表型(M1、M2、M4等),释放不同细胞因子,受多种信号通路(PI3K/Akt、TLR4、TGF-β/Smads等)调控,并在心血管疾病中发挥其他功能。M1通过分泌促炎因子启动并维持炎症,M2通过分泌抗炎因子参与炎症消退和组织修复。因此,通过调节信号通路,减少巨噬细胞聚集,促进巨噬细胞向M2极化,或恢复M1/M2平衡,以改善炎症微环境并延缓心血管疾病进展。