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首页> 外文期刊>Frontiers in bioscience: a journal and virtual library >Blood coagulation-dependent inflammation. Coagulation-dependent inflammation and inflammation-dependent thrombosis.
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Blood coagulation-dependent inflammation. Coagulation-dependent inflammation and inflammation-dependent thrombosis.

机译:凝血依赖性炎症。凝血依赖性炎症和炎症依赖性血栓形成。

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Hemostatic serine proteinases-thrombin, Factor VIIa, Factor Xa, play the central role in blood coagulation and thrombosis. Activation of coagulation and generation of active proteinases is initiated by tissue factor (TF) that is expressed by cells of the innate immune system and endothelial cells after tissue damage and cell activation induced by trauma, infection, hypoxia and other cell injury. Coagulation and inflammation are the essential part of the defensive host response. These processes have several connecting points account for the associate and/or the interaction between coagulation and inflammation pathways. The first link between these processes is endothelium, which after damage expresses the adhesive proteins (vWF,P-selectin), inductors and receptors, involved in both coagulation and inflammation. The second link is platelets, which stored in and after activation release proteins with procoagulant and proinflammatory properties. The third link is the serine proteinases, which produced for blood coagulation and activate via its specifical receptors--PARs (proteinase activated receptors) the cells of both coagulation and inflammation system thereby controlling these processes. The generation of these proteinases is initiated by tissue factor (TF) which triggers blood coagulation at sites of tissue injury by selective binding of FVIIa. TF/VIIa complexes with substrate--FX that is activated to FXa. TF/VIIa/Xa can activate both the inflammatory responses of endothelial and other cells and also blood coagulation through stimulation of thrombin generation. This review summarizes the latest data on the blood coagulation activation that include generation of active surface for coagulation, generation of hemostatic serine proteinases and its role as signalling molecules that via PARs and other receptors involved in regulation and control of the interaction of blood coagulation and inflammation and illustrates the potential for therapeutic intervention.
机译:止血丝氨酸蛋白酶-凝血酶,VIIa因子,Xa因子在血液凝结和血栓形成中起着核心作用。凝血的激活和活性蛋白酶的产生是由组织因子(TF)启动的,组织因子是由创伤,感染,缺氧和其他细胞损伤引起的组织损伤和细胞活化后,先天免疫系统细胞和内皮细胞表达的。凝血和炎症是防御宿主反应的重要部分。这些过程有几个连接点,说明了凝血和炎症途径之间的联系和/或相互作用。这些过程之间的第一个联系是内皮细胞,内皮细胞在受损后表达参与凝血和炎症的粘附蛋白(vWF,P-选择素),诱导剂和受体。第二个环节是血小板,血小板储存在活化过程中和活化后释放具有促凝和促炎特性的蛋白质。第三个环节是丝氨酸蛋白酶,其用于血液凝结,并通过其特异性受体PARs(蛋白酶激活的受体)激活凝结和炎症系统的细胞,从而控制这些过程。这些蛋白酶的产生是由组织因子(TF)启动的,该因子通过FVIIa的选择性结合触发组织损伤部位的血液凝结。 TF / VIIa与被激活为FXa的底物FX形成复合物。 TF / VIIa / Xa既可以激活内皮细胞和其他细胞的炎症反应,又可以通过刺激凝血酶生成来激活凝血功能。这篇综述总结了有关凝血激活的最新数据,包括凝血的活性表面的产生,止血丝氨酸蛋白酶的产生及其作为信号分子的作用,这些分子通过PAR和其他参与调节和控制凝血与炎症相互作用的受体并说明了治疗干预的潜力。

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