Rosenthal K L, Tompkins W A, Wachsman J T
Mol Cell Biochem. 1977 Apr 12;15(2):149-53. doi: 10.1007/BF01793338.
Fibrinolytic activity was studied in a number of different established as well as secondary human cell cultures derived from both malignant and normal tissues. The ability to degrade [25I]-labeled fibrin was found to be characteristic of some malignant cultures as well as some normal cultures, and to be dependent upon the presence of serum. For the most part, this activity was detected in cultures with a relatively short in vitro passage history (less than 30 passages). Low passaged colon and rectal carcinoma cells, HCT-8 and HRT-18, as well as normal rectal, colon and foreskin fibroblasts were positive for fibrinolytic activity, while long established (greater than 100 passages) cultures of malignant cells (colon carcinoma, HeLa, Hep-2, KB) as well as normal cells (HEI, AV3) were negative. It is proposed that although some normal cells synthesize plasminogen activators, the fibrinolytic capability of both malignant and normal cells may be lost on prolonged in vitro cultivation.
在源自恶性和正常组织的多种不同的已建立的以及传代的人细胞培养物中研究了纤溶活性。发现降解[25I]标记的纤维蛋白的能力是一些恶性培养物以及一些正常培养物的特征,并且依赖于血清的存在。在很大程度上,这种活性在体外传代历史相对较短(少于30代)的培养物中被检测到。低代传的结肠和直肠癌细胞HCT-8和HRT-18,以及正常的直肠、结肠和包皮成纤维细胞具有纤溶活性,而长期建立的(超过100代)恶性细胞(结肠癌、HeLa、Hep-2、KB)以及正常细胞(HEI、AV3)培养物则为阴性。有人提出,虽然一些正常细胞合成纤溶酶原激活剂,但恶性和正常细胞的纤溶能力可能会在长期体外培养中丧失。