镉、血管性血友病因子与血管老化。

Xia Wang, Maria N Starodubtseva, Carolyn M Kapron, Ju Liu
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引用次数: 1

摘要

血管老化是导致心血管疾病的一个主要因素。血管老化是由氧化应激和炎症引起的内皮细胞功能障碍引起的,其特征是血管壁增厚和硬化。血管性血友病因子(vWF)是一种糖蛋白,因其在凝血中的作用而闻名,血浆vWF水平随着年龄的增长而增加。vWF升高促进血栓形成、动脉粥样硬化斑块形成、炎症和血管平滑肌细胞增殖。镉(Cd)是一种与心血管疾病发病率和死亡率增加有关的环境污染物。在低浓度下,Cd激活内皮细胞的促生存信号,但增加内膜-中膜厚度和动脉粥样硬化。在体内和体外,非细胞毒性剂量的Cd也增加内皮细胞vWF的表达和分泌。在这篇综述中,我们总结了vWF促进血管衰老相关病理和cd诱导vWF表达的分子机制。此外,我们提出暴露于低剂量镉是血管老化的一个危险因素,通过血浆vWF升高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cadmium, von Willebrand factor and vascular aging.

Cadmium, von Willebrand factor and vascular aging.

Vascular aging is a major contributing factor to cardiovascular disease. The aged blood vessels, characterized by vascular wall thickening and stiffening, are instigated by endothelial cell dysfunction induced by oxidative stress and inflammation. von Willebrand Factor (vWF) is a glycoprotein known for its role in coagulation, and plasma levels of vWF are increased with age. Elevated vWF promotes thrombosis, atherosclerotic plaque formation, inflammation and proliferation of vascular smooth muscle cells. Cadmium (Cd) is an environmental pollutant associated with increased morbidity and mortality of cardiovascular disease. At low concentrations, Cd activates pro-survival signaling in endothelial cells, however enhances intima-media thickness and atherogenesis. A non-cytotoxic dose of Cd also increases endothelial vWF expression and secretion in vivo and in vitro. In this review, we summarize the molecular mechanisms underlying vWF-promoted vascular aging-associated pathologies and Cd-induced vWF expression. In addition, we propose that exposure to low-dose Cd is a risk factor for vascular aging, through elevation of plasma vWF.

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