首页|CXCL12/MIF-CXCR4生物轴在治疗动脉粥样硬化应用中的研究进展

CXCL12/MIF-CXCR4生物轴在治疗动脉粥样硬化应用中的研究进展

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动脉粥样硬化(As)是世界范围内死亡率和发病率高的主要原因之一.趋化因子及其受体参与As的发病机制.CXC趋化因子配体12(CXCL12)是趋化因子家族的成员,巨噬细胞迁移抑制因子(MIF)是趋化因子样功能趋化因子,CXCL12和MIF共同通过CXC趋化因子受体4(CXCR4)在As中发挥着重要的作用.CXCL12-CXCR4生物轴是一条重要的趋化因子/趋化因子受体轴,能够调控细胞增殖、动员、分化、归巢和趋化等多种生物学行为,大量研究发现其广泛影响着与As相关的多种细胞,与As斑块的形成、发展密切相关.因此,CXCL12/MIF-CXCR4生物轴有望成为更加精确的As治疗靶点,调控CXCL12/MIF-CXCR4生物轴策略为As的防治提供新的思路.
Advances in the CXCL12/MIF-CXCR4 bioaxis for therapeutic atherosclerosis appli-cations
Atherosclerosis(As)is one of the major causes of high mortality and morbidity worldwide.Chemokines and their receptors are involved in the pathogenesis of As.CXC chemokine ligand 12(CXCL12)is a mem-ber of the chemokine family,and macrophage migration inhibition factor(MIF)is a chemokine like functional chemokine,CXCL12 and MIF together play important roles in As through CXC chemokine receptor 4(CXCR4).The CXCL12-CX-CR4 bioaxis is an important chemokine/chemokine receptor axis that can regulate various biological behaviors such as cell proliferation,mobilization,differentiation,homing,and chemotaxis.Numerous studies have found that it widely affects various cells related to As and is closely related to the formation and development of As plaques.Therefore,the CXCL12/MIF-CXCR4 bioaxis is expected to become a more precise target for As treatment,and regulating the CXCL12/MIF-CXCR4 bioaxis strategy provides new ideas for the prevention and treatment of As.

CXCL12/MIF-CXCR4 bioaxismacrophage migration inhibition factoratherosclerosis

梁子舜、蔡晶、乔彤

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南京中医药大学鼓楼临床医学院血管外科

南京大学医学院附属鼓楼医院血管外科,江苏省南京市 210008

CXCL12/MIF-CXCR4生物轴 巨噬细胞迁移抑制因子 动脉粥样硬化

国家自然科学基金青年基金项目江苏省卫生健康委医学科研项目

82200543ZD2021056

2024

中国动脉硬化杂志
中国病理生理学会 南华大学

中国动脉硬化杂志

CSTPCD
影响因子:1.086
ISSN:1007-3949
年,卷(期):2024.32(9)
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