Lecander I, Roblin R, Astedt B
Br J Haematol. 1984 Jul;57(3):407-12. doi: 10.1111/j.1365-2141.1984.tb02914.x.
The inhibitory effect of a placental urokinase inhibitor on the one- and two-chain form of melanoma cell derived plasminogen activator (PA) was investigated. The melanoma cell PA has been shown to be similar to or identical with the PA found in normal tissue. With constant concentration of placental inhibitor the rate of inhibition of the two-chain form was fast in contrast to that of the one-chain form. With constant incubation time but increasing concentrations of the placental inhibitor the two-chain form was inactivated to a greater extent at lower concentrations of placental inhibitor than was the one-chain form. The increased reactivity of the two-chain form of melanoma PA compared to the single-chain form may explain the role of tissue PA in achieving high local concentrations of PA activity which facilitate selective fibrin clot lysis.
研究了胎盘尿激酶抑制剂对黑色素瘤细胞源性纤溶酶原激活剂(PA)单链和双链形式的抑制作用。黑色素瘤细胞PA已被证明与正常组织中发现的PA相似或相同。在胎盘抑制剂浓度恒定的情况下,双链形式的抑制速率较快,与单链形式形成对比。在孵育时间恒定但胎盘抑制剂浓度增加的情况下,双链形式在较低浓度的胎盘抑制剂下比单链形式在更大程度上失活。黑色素瘤PA双链形式与单链形式相比反应性增加,这可能解释了组织PA在实现高局部PA活性浓度以促进选择性纤维蛋白凝块溶解中的作用。