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凝血因子IX血管内结合位点的体内证据。

In vivo evidence of intravascular binding sites for coagulation factor IX.

作者信息

Stern D M, Knitter G, Kisiel W, Nawroth P P

出版信息

Br J Haematol. 1987 Jun;66(2):227-32. doi: 10.1111/j.1365-2141.1987.tb01303.x.

Abstract

Previous studies have demonstrated that factors IX/IXa bind to specific sites on the surfaces of cultured and native endothelium in vitro and that these sites should be occupied with factor IX in homeostasis. Since factor IX of different species binds to endothelium in a similar manner, we examined if infusion of heterologous factor IX into an animal should result in displacement of host factor IX antigen from its vessel wall site. Experiments were carried out in baboons with a large excess of bovine factor IX employing species-specific radioimmunoassays. The results indicate that infusion of bovine factor IX or active site-blocked factor IXa, but not prothrombin, resulted in a dose-dependent rise in the plasma level of baboon factor IX antigen. This suggested that the infused factor IX was displacing the host clotting factor from some reservoir easily accessible to the intravascular space. Consistent with this hypothesis, infusion of 125I-factor IX demonstrated accumulation in multiple organs. Radioiodinated factor IX comigrating with the initial tracer on SDS-PAGE could be eluted from the luminal surface of pulmonary artery and aortic segments. 125I-factor IX was not significantly associated with cellular elements of the blood. These results suggest that there is a pool of non-circulating factor IX which is accessible to the intravascular space, widely distributed and involves endothelium.

摘要

先前的研究表明,凝血因子IX/IXa在体外可与培养的及天然内皮细胞表面的特定位点结合,且在体内平衡状态下这些位点应由凝血因子IX占据。由于不同物种的凝血因子IX以相似的方式与内皮细胞结合,我们研究了向动物体内输注异源凝血因子IX是否会导致宿主凝血因子IX抗原从其血管壁位点上被取代。我们使用物种特异性放射免疫分析法,在狒狒身上用大量过量的牛凝血因子IX进行了实验。结果表明,输注牛凝血因子IX或活性位点被阻断的凝血因子IXa,但不包括凝血酶原,会导致狒狒凝血因子IX抗原的血浆水平呈剂量依赖性升高。这表明输注的凝血因子IX正在从血管内空间易于进入的某些储存库中取代宿主凝血因子。与该假设一致的是,输注125I-凝血因子IX显示其在多个器官中蓄积。在SDS-PAGE上与初始示踪剂共迁移的放射性碘化凝血因子IX可从肺动脉和主动脉段的管腔表面洗脱下来。125I-凝血因子IX与血液中的细胞成分无明显关联。这些结果表明,存在一个血管内空间可进入的、分布广泛且涉及内皮细胞的非循环凝血因子IX池。

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