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靶向 LOX-1 在动脉粥样硬化和血管病变中的作用:当前的认识和未来的展望。

Targeting LOX-1 in atherosclerosis and vasculopathy: current knowledge and future perspectives.

机构信息

Department of Preventive Medicine, School of Public Health, Zunyi Medical University, Zunyi, Guizhou, China.

Division of Laboratory Medicine, Department of Pathology and Microbiology, Nihon University School of Medicine, Tokyo, Japan.

出版信息

Ann N Y Acad Sci. 2019 May;1443(1):34-53. doi: 10.1111/nyas.13984. Epub 2018 Nov 1.

Abstract

LOX-1 (lectin-like oxidized low-density lipoprotein receptor-1; also known as OLR1) is the dominant receptor that recognizes and internalizes oxidized low-density lipoproteins (ox-LDLs) in endothelial cells. Several genetic variants of LOX-1 are associated with the risk and severity of coronary artery disease. The LOX-1-ox-LDL interaction induces endothelial dysfunction, leukocyte adhesion, macrophage-derived foam cell formation, smooth muscle cell proliferation and migration, and platelet activation. LOX-1 activation eventually leads to the rupture of atherosclerotic plaques and acute cardiovascular events. In addition, LOX-1 can be cleaved to generate soluble LOX-1 (sLOX-1), which is a useful diagnostic and prognostic marker for atherosclerosis-related diseases in human patients. Of therapeutic relevance, several natural products and clinically used drugs have emerged as LOX-1 inhibitors that have antiatherosclerotic actions. We hereby provide an updated overview of role of LOX-1 in atherosclerosis and associated vascular diseases, with an aim to highlighting the potential of LOX-1 as a novel theranostic tool for cardiovascular disease prevention and treatment.

摘要

LOX-1(凝集素样氧化低密度脂蛋白受体-1;也称为 OLR1)是识别和内化内皮细胞中氧化低密度脂蛋白(ox-LDL)的主要受体。几种 LOX-1 遗传变异与冠心病的风险和严重程度有关。LOX-1-ox-LDL 相互作用可诱导内皮功能障碍、白细胞黏附、巨噬细胞源性泡沫细胞形成、平滑肌细胞增殖和迁移以及血小板激活。LOX-1 的激活最终导致动脉粥样硬化斑块破裂和急性心血管事件。此外,LOX-1 可被切割生成可溶性 LOX-1(sLOX-1),这是人类动脉粥样硬化相关疾病的一种有用的诊断和预后标志物。具有治疗相关性的是,几种天然产物和临床使用的药物已被证明是 LOX-1 抑制剂,具有抗动脉粥样硬化作用。在此,我们提供了 LOX-1 在动脉粥样硬化和相关血管疾病中的作用的最新概述,旨在强调 LOX-1 作为心血管疾病预防和治疗的新型治疗工具的潜力。

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