首页|T细胞代谢重编程调控动脉粥样硬化进程的作用及机制研究

T细胞代谢重编程调控动脉粥样硬化进程的作用及机制研究

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动脉粥样硬化是多种心血管疾病的病理学基础,而T细胞则是其发生发展过程中的重要免疫细胞。T细胞可极化成不同的表型,在动脉粥样硬化发展过程中发挥相应的功能,如Th1和Th17细胞具有促炎作用,而Th2和Treg细胞具有抑炎作用,不同的T细胞亚群比例和功能失衡也是动脉粥样硬化斑块形成与发展的重要原因。在不同的微环境中代谢重编程通过调节代谢途径来改变T细胞的分化方向,进而改变动脉粥样硬化的发展方向。现就T细胞在动脉粥样硬化中的促炎与抑炎作用做一综述,重点介绍促炎性或抑炎性T细胞的代谢重编程对动脉粥样硬化的调控及其mTOR和AMPK信号转导的分子机制。
Role and Mechanism of T Cell Metabolic Reprogramming in Regulation of Atherosclerosis Progression
Atherosclerosis is the pathological basis of a variety of cardiovascular diseases,and T cells are important immune cells in the process of its development.T cells can be polarized into different phenotypes and play corresponding roles in the development of atherosclerosis.For example,Th1 and Th17 cells have pro-inflammatory effects,while Th2 and Treg cells have anti-inflammatory effects.The proportion and functional imbalance of different T cell subsets are also important reasons for the formation and development of atherosclerotic plaques.Metabolic reprogramming changes the differentiation direction of T cells by regulating metabolic pathways in different microenvironments,thereby changing the development direction of atherosclerosis.This article reviews the proinflammatory and anti-inflammatory roles of T cells in atherosclerosis,focusing on the regulation of atherosclerosis by metabolic reprogramming of proinflammatory/anti-inflammatory T cells and the molecular mechanisms underlying mTOR and AMPK signaling.

AtherosclerosisT cellMetabolic reprogrammingSignal pathway

常姝烨、安恬慧、王朝晖

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华中科技大学同济医学院附属协和医院老年科,湖北武汉 430000

动脉粥样硬化 T细胞 代谢重编程 信号通路

国家自然科学基金

82101662

2024

心血管病学进展
成都市心血管病研究所,成都市第三人民医院

心血管病学进展

CSTPCD
影响因子:0.932
ISSN:1004-3934
年,卷(期):2024.45(9)