Mukhina S A, Stepanova V V, Matveev M Iu, Domogatskiĭ S P, Tkachuk V A
Moscow State University, Russia.
Vopr Med Khim. 1998 Jan-Feb;44(1):84-90.
The dependence of urokinase (uPA) secretion on basic fibroblast growth factor (bFGF) and platelet-deprived growth factor (PDGF BB) was investigated by using of cultured rat aortic smooth muscle cells (SMC). Growth factors stimulated secretion of urokinase with two-phase kinetics within 1-60 minutes. Namely, "apparent" concentration of uPA in the conditioned media rised to 12.5 nM within the first 1-2 min and 5.8 nM after 30 min of cell stimulation by growth factors, and decreased to basal level at 5 min after stimulation of the cells. The character of uPA-secretion kinetics was similar in response to both growth factors, but the level of secreted uPA was higher in case of PDGF BB. We have shown that this decrease of uPA content in conditioned media is not related to the binding of uPA to the cell surface receptors or extracellular matrix proteins. One can suppose that urokinase secreted within 5 minutes could bind to secretory protein which nature has to be identified. But it was established that this secretory protein, complexing urokinase in cultured media, is not identical to the plasminogen activator inhibitor type 1 (PAI-1).
通过使用培养的大鼠主动脉平滑肌细胞(SMC),研究了尿激酶(uPA)分泌对碱性成纤维细胞生长因子(bFGF)和血小板衍生生长因子(PDGF BB)的依赖性。生长因子在1 - 60分钟内以两相动力学刺激尿激酶的分泌。具体而言,在生长因子刺激细胞后的最初1 - 2分钟内,条件培养基中uPA的“表观”浓度升至12.5 nM,30分钟后为5.8 nM,并在刺激细胞后5分钟降至基础水平。两种生长因子刺激下uPA分泌动力学特征相似,但PDGF BB刺激时分泌的uPA水平更高。我们已经表明,条件培养基中uPA含量的这种下降与uPA与细胞表面受体或细胞外基质蛋白的结合无关。可以推测,5分钟内分泌的尿激酶可能与一种性质有待确定的分泌蛋白结合。但已确定,在培养基中与尿激酶形成复合物的这种分泌蛋白与纤溶酶原激活物抑制剂1型(PAI - 1)不同。