Hisazumi H, Andersson L, Collins V P
Urol Res. 1977;5(3):133-9. doi: 10.1007/BF00256867.
Three human bladder carcinoma cell lines, T 24, RT 4, and MANO, a human bladder nonmalignant epithelial cell line, HCV-29, and a human lung fibroblast line, 460 H1, were investigated for their ability to induce fibrinolytic, urokinase and plasmin inhibitory activities in cell culture, using serum-free medium, for up to 36 h. Generally, the non-malignant cell line and the fibroblast line had a greater ability to produce urokinase inhibitor than did the malignant cell lines. The amount produced varied greatly between cells and over the study period. A low concentration of plasminogen activator, immunologically identical with urokinase, and its accumulation in culture supernate were found with RT 4 after 12 h and 24 h cultivations, whereas no plasminogen activator was detected in all other cell lines for periods up to 36 h. No plasmin, non-specific protease or plasmin inhibitory activities were detected in any of the supernates from the cell lines.
使用无血清培养基,对三种人膀胱癌细胞系T 24、RT 4和MANO、一种人膀胱非恶性上皮细胞系HCV - 29以及一种人肺成纤维细胞系460 H1进行了研究,观察它们在细胞培养中诱导纤溶、尿激酶和纤溶酶抑制活性的能力,培养时间长达36小时。一般来说,非恶性细胞系和成纤维细胞系产生尿激酶抑制剂的能力比恶性细胞系更强。细胞之间以及在整个研究期间产生的量差异很大。在培养12小时和24小时后,RT 4细胞培养上清液中发现了低浓度的、与尿激酶免疫相同的纤溶酶原激活剂及其积累,而在长达36小时的时间内,在所有其他细胞系中均未检测到纤溶酶原激活剂。在任何细胞系的上清液中均未检测到纤溶酶、非特异性蛋白酶或纤溶酶抑制活性。