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凝血酶对人包皮微血管内皮细胞纤溶酶原激活剂及纤溶酶原激活物抑制剂-1产生的影响。

Effect of thrombin on the production of plasminogen activators and PA inhibitor-1 by human foreskin microvascular endothelial cells.

作者信息

Van Hinsbergh V W, Sprengers E D, Kooistra T

出版信息

Thromb Haemost. 1987 Apr 7;57(2):148-53.

PMID:3496679
Abstract

Human foreskin microvascular endothelial cells synthesize and release tissue-type plasminogen activator (t-PA) in similar amounts as do endothelial cells from umbilical cord artery and vein. Human thrombin increases the production of t-PA by these cells, which could be visualized from 8 h after addition of 0.1-5 units/ml thrombin by fibrin autography after SDS polyacrylamide gel electrophoresis of the endothelial cell conditioned media. Thrombin also increased the secretion of t-PA antigen. Together with t-PA, human microvascular cells release urokinase-type plasminogen activator (u-PA) antigen and endothelial cell-type PA inhibitor, PA inhibitor-1, which were both demonstrated by specific immunoprecipitation from radiolabeled endothelial cell conditioned medium. Thrombin increases the release of u-PA antigen, but no u-PA activity could be demonstrated. Thrombin induced a two-fold stimulation of the synthesis and secretion of PA inhibitor-1 antigen. At 0.1 unit/ml thrombin also an increase in PA inhibitor activity was found. At high concentrations of thrombin a decrease of PA inhibitor activity was found, due to the conversion of the active 46 kD PA inhibitor-1 into a 42 kD product without PA inhibitor activity. Our data indicate that interaction of thrombin with microvascular endothelial cells will shift the balance between t-PA, u-PA and PA inhibitor-1, and thus affects the regulation of fibrinolysis.

摘要

人包皮微血管内皮细胞合成并释放组织型纤溶酶原激活物(t-PA)的量与脐动脉和脐静脉内皮细胞相似。人凝血酶可增加这些细胞t-PA的产生,在内皮细胞条件培养基经SDS聚丙烯酰胺凝胶电泳后进行纤维蛋白自显影,从加入0.1 - 5单位/毫升凝血酶8小时后即可观察到。凝血酶还增加了t-PA抗原的分泌。人微血管细胞除释放t-PA外,还释放尿激酶型纤溶酶原激活物(u-PA)抗原和内皮细胞型PA抑制剂即PA抑制剂-1,这两者均可通过对放射性标记的内皮细胞条件培养基进行特异性免疫沉淀得到证实。凝血酶增加u-PA抗原的释放,但未检测到u-PA活性。凝血酶使PA抑制剂-1抗原的合成和分泌增加了两倍。在0.1单位/毫升凝血酶时,还发现PA抑制剂活性增加。在高浓度凝血酶时,由于活性46kD的PA抑制剂-1转化为无PA抑制剂活性的42kD产物,导致PA抑制剂活性降低。我们的数据表明,凝血酶与微血管内皮细胞的相互作用将改变t-PA、u-PA和PA抑制剂-1之间的平衡,从而影响纤溶的调节。

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