Miles L A, Levin E G, Plescia J, Collen D, Plow E F
Department of Immunology, Research Institute of Scripps Clinic, La Jolla, CA 92037.
Blood. 1988 Aug;72(2):628-35.
Endothelial cells are centrally involved in regulation of fibrinolysis, and receptors for plasminogen and urokinase provide a mechanism by which cells can regulate their fibrinolytic function. Therefore, the existence and characteristics of receptors for these fibrinolytic components on cultured human umbilical vein endothelial cells were examined. We verified the presence of plasminogen receptors on these cells (Kd = 2.1 +/- 1.3 mumol/L, and 1.8 +/- 1.3 x 10(7) binding sites/cell). These binding parameters and other characteristics indicate that these receptors are closely related to the plasminogen receptors on many circulating and adherent cells. Specific binding sites that interact with two-chain urokinase of mol wt 55,000 with a dissociation constant of 2.1 +/- 1.7 nmol/L, with 2.9 +/- 2.9 x 10(5) sites/cell were also identified. Single-chain urokinase of mol wt 55,000, but not the two-chain degradation product of mol wt 33,000 bound to the cells, implicating the amino-terminal aspects of the ligand in receptor recognition. When endothelial cells were stimulated with thrombin, an agent that modulates their fibrinolytic potential, both receptor types were modestly affected; urokinase binding increased 17%, whereas plasminogen binding decreased 19%. The presence and modulation of plasminogen and urokinase receptors provide a potentially important additional mechanism by which endothelial cells may regulate fibrinolysis.
内皮细胞在纤维蛋白溶解调节中起核心作用,纤溶酶原和尿激酶的受体提供了一种细胞可调节其纤维蛋白溶解功能的机制。因此,我们检测了培养的人脐静脉内皮细胞上这些纤维蛋白溶解成分受体的存在及特性。我们证实了这些细胞上存在纤溶酶原受体(解离常数Kd = 2.1 +/- 1.3 μmol/L,每个细胞有1.8 +/- 1.3 x 10(7)个结合位点)。这些结合参数和其他特性表明,这些受体与许多循环细胞和黏附细胞上的纤溶酶原受体密切相关。还鉴定出了与分子量为55,000的双链尿激酶相互作用的特异性结合位点,其解离常数为2.1 +/- 1.7 nmol/L,每个细胞有2.9 +/- 2.9 x 10(5)个位点。分子量为55,000的单链尿激酶能与细胞结合,而分子量为33,000的双链降解产物则不能,这表明配体的氨基末端参与受体识别。当用凝血酶刺激内皮细胞时(凝血酶是一种可调节其纤维蛋白溶解潜能的物质),两种受体类型均受到一定影响;尿激酶结合增加了17%,而纤溶酶原结合减少了19%。纤溶酶原和尿激酶受体的存在及调节为内皮细胞调节纤维蛋白溶解提供了一种潜在的重要额外机制。