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组织因子与动脉粥样硬化和动脉血栓形成。

Tissue factor in atherosclerosis and atherothrombosis.

机构信息

UNC Blood Research Center, Division of Hematology and Oncology, Department of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

UNC Blood Research Center, Division of Hematology and Oncology, Department of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

出版信息

Atherosclerosis. 2020 Aug;307:80-86. doi: 10.1016/j.atherosclerosis.2020.06.003. Epub 2020 Jul 3.

Abstract

Atherosclerosis is a chronic inflammatory disease that is characterized by the formation of lipid rich plaques in the wall of medium to large sized arteries. Atherothrombosis represents the terminal manifestation of this pathology in which atherosclerotic plaque rupture or erosion triggers the formation of occlusive thrombi. Occlusion of arteries and resultant tissue ischemia in the heart and brain causes myocardial infarction and stroke, respectively. Tissue factor (TF) is the receptor for the coagulation protease factor VIIa, and formation of the TF:factor VIIa complex triggers blood coagulation. TF is expressed at high levels in atherosclerotic plaques by both macrophage-derived foam cells and vascular smooth muscle cells, as well as extracellular vesicles derived from these cells. Importantly, TF mediated activation of coagulation is critically important for arterial thrombosis in the setting of atherosclerotic disease. The major endogenous inhibitor of the TF:factor VIIa complex is TF pathway inhibitor 1 (TFPI-1), which is also present in atherosclerotic plaques. In mouse models, increased or decreased expression of TFPI-1 has been found to alter atherosclerosis. This review highlights the contribution of TF-dependent activation of coagulation to atherthrombotic disease.

摘要

动脉粥样硬化是一种慢性炎症性疾病,其特征是中到大动脉壁中富含脂质的斑块形成。动脉粥样硬化血栓形成代表了这种病理学的终末表现,其中动脉粥样硬化斑块破裂或侵蚀触发了闭塞性血栓的形成。动脉阻塞和由此导致的心脏和大脑组织缺血分别导致心肌梗死和中风。组织因子 (TF) 是凝血蛋白酶因子 VIIa 的受体,TF:factor VIIa 复合物的形成引发血液凝固。TF 由巨噬细胞衍生的泡沫细胞和血管平滑肌细胞以及这些细胞衍生的细胞外囊泡以高水平表达于动脉粥样硬化斑块中。重要的是,TF 介导的凝血激活对于动脉粥样硬化疾病中的动脉血栓形成至关重要。TF:factor VIIa 复合物的主要内源性抑制剂是组织因子途径抑制剂 1(TFPI-1),其也存在于动脉粥样硬化斑块中。在小鼠模型中,TFPI-1 的表达增加或减少已被发现可改变动脉粥样硬化。本综述强调了 TF 依赖性凝血激活对动脉粥样硬化血栓形成疾病的贡献。

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