Badenoch-Jones P, Ramshaw I A, Grant A
Aust J Exp Biol Med Sci. 1985 Jun;63 ( Pt 3):343-52. doi: 10.1038/icb.1985.40.
Expression of plasminogen activator (PA) activity may be an important factor in the ability of tumour cells to metastasize; however, not all metastatic cells produce detectable PA activity. Conditioned culture media from revertant metastatic clones of cells derived by fusion of metastatic and non-metastatic rat mammary adenocarcinoma cells were found to contain a potent inhibitor of PA. This inhibited thrombin, human urokinase (UK) and tumour-derived PA, but not plasmin or trypsin. Inhibition was still obtained after polyacrylamide gel electrophoresis in the presence of sodium dodecyl sulphate (SDS-PAGE) of mixtures of PA and inhibitor, followed by development of PA activity on fibrin overlays. The PA inhibitor eluted from Sephadex G-200 over a broad M.wt. range (35,000-80,000) and was inactivated by heating to 70 degrees for 30 min. The appearance of inhibitory activity in the culture media was time-dependent and could be reduced by incubation of cells with cycloheximide. Because of these findings, the possible presence of inhibitors should be considered in investigations into the role of PA in the metastatic process.
纤溶酶原激活物(PA)活性的表达可能是肿瘤细胞转移能力的一个重要因素;然而,并非所有转移细胞都能产生可检测到的PA活性。通过将转移性和非转移性大鼠乳腺腺癌细胞融合而获得的细胞的回复转移性克隆的条件培养基中发现含有一种强效的PA抑制剂。它能抑制凝血酶、人尿激酶(UK)和肿瘤来源的PA,但不能抑制纤溶酶或胰蛋白酶。在十二烷基硫酸钠存在下进行聚丙烯酰胺凝胶电泳(SDS-PAGE),将PA和抑制剂的混合物进行电泳,然后在纤维蛋白覆盖物上检测PA活性,仍能观察到抑制作用。PA抑制剂从Sephadex G-200上洗脱时分子量范围较宽(35,000 - 80,000),加热至70摄氏度30分钟会使其失活。培养基中抑制活性的出现具有时间依赖性,用环己酰亚胺处理细胞可降低这种活性。基于这些发现,在研究PA在转移过程中的作用时应考虑抑制剂可能的存在。