Yang Pinglian, Rong Xiaoling, Gao Zhechang, Wang Jiaojiao, Liu Zhiping
State Key Laboratory of Bioactive Molecules and Druggability Assessment, Guangdong Province Key Laboratory of Pharmacodynamic Constituents of TCM and New Drugs Research, International Cooperative Laboratory of Traditional Chinese Medicine Modernization and Innovative Drug Discovery of Chinese Ministry of Education (MOE), College of Pharmacy, Jinan University, Guangzhou 510632, China.
School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China.
Pharmacol Res. 2025 Feb;212:107588. doi: 10.1016/j.phrs.2025.107588. Epub 2025 Jan 6.
Atherosclerosis, a multifactorial progressive inflammatory disease, is the common pathology underlying cardiovascular and cerebrovascular diseases. The macrophage plasticity is involved in the pathogenesis of atherosclerosis. With the advance of metabolomics and epigenetics, metabolites/metabolic and epigenetic modification such as DNA methylation, histone modification and noncoding RNA, play a crucial role in macrophage polarization and the progression of atherosclerosis. Herein, we provide a comprehensive review of the essential role of metabolic and epigenetic regulation, as well as the crosstalk between the two in regulating macrophage polarization in atherosclerosis. We also highlight the potential therapeutic strategies of regulating macrophage polarization via epigenetic and metabolic modifications for atherosclerosis, and offer recommendations to advance our knowledge of the roles of metabolic-epigenetic crosstalk in macrophage polarization in the context of atherosclerosis. Fundamental studies that elucidate the mechanisms by which metabolic and epigenetic regulation of macrophage polarization influence atherosclerosis will pave the way for novel therapeutic approaches.
动脉粥样硬化是一种多因素的进行性炎症性疾病,是心脑血管疾病的共同病理基础。巨噬细胞可塑性参与动脉粥样硬化的发病机制。随着代谢组学和表观遗传学的发展,代谢物/代谢和表观遗传修饰,如DNA甲基化、组蛋白修饰和非编码RNA,在巨噬细胞极化和动脉粥样硬化进展中起关键作用。在此,我们全面综述了代谢和表观遗传调控的重要作用,以及两者在调节动脉粥样硬化中巨噬细胞极化的相互作用。我们还强调了通过表观遗传和代谢修饰调节巨噬细胞极化治疗动脉粥样硬化的潜在策略,并提出建议以增进我们对动脉粥样硬化背景下代谢-表观遗传相互作用在巨噬细胞极化中作用的认识。阐明巨噬细胞极化的代谢和表观遗传调控影响动脉粥样硬化机制的基础研究将为新的治疗方法铺平道路。