ClC-3:一种新的有希望的动脉粥样硬化治疗靶点

IF 2.5 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Dun Niu, Lanfang Li, Zhizhong Xie
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引用次数: 3

摘要

氯离子通道3 (Cl -3)是一种Cl-/H+反转运蛋白,是体积调节氯离子通道(vrcc)的一员。ClC-3可能是通过调节蛋白磷酸化激活炎症相关信号通路的重要介质。越来越多的研究表明,ClC-3过表达在介导血浆低密度脂蛋白水平升高、血管内皮功能障碍、巨噬细胞的促炎激活、血管平滑肌细胞(VSMCs)的超增殖和超迁移以及氧化应激和泡沫细胞形成等过程中起着至关重要的作用,是动脉壁粥样硬化斑块形成的主要因素。本文对ClC-3的分子结构和经典功能进行了综述。我们进一步讨论了它在动脉粥样硬化过程中的新作用。总之,我们探讨了ClC-3作为动脉粥样硬化治疗靶点的潜在作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ClC-3: A Novel Promising Therapeutic Target for Atherosclerosis.

Chloride channel 3 (ClC-3), a Cl-/H+ antiporter, has been well established as a member of volume-regulated chloride channels (VRCCs). ClC-3 may be a crucial mediator for activating inflammation-associated signaling pathways by regulating protein phosphorylation. A growing number of studies have indicated that ClC-3 overexpression plays a crucial role in mediating increased plasma low-density lipoprotein levels, vascular endothelium dysfunction, pro-inflammatory activation of macrophages, hyper-proliferation and hyper-migration of vascular smooth muscle cells (VSMCs), as well as oxidative stress and foam cell formation, which are the main factors responsible for atherosclerotic plaque formation in the arterial wall. In the present review, we summarize the molecular structures and classical functions of ClC-3. We further discuss its emerging role in the atherosclerotic process. In conclusion, we explore the potential role of ClC-3 as a therapeutic target for atherosclerosis.

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来源期刊
CiteScore
6.00
自引率
0.00%
发文量
33
审稿时长
6-12 weeks
期刊介绍: Journal of Cardiovascular Pharmacology and Therapeutics (JCPT) is a peer-reviewed journal that publishes original basic human studies, animal studies, and bench research with potential clinical application to cardiovascular pharmacology and therapeutics. Experimental studies focus on translational research. This journal is a member of the Committee on Publication Ethics (COPE).
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