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蛋白酶抑制剂可抑制疱疹病毒转化细胞的纤溶活性。

Protease inhibitors suppress fibrinolytic activity of herpesvirus-transformed cells.

作者信息

Adelman S F, Howett M K, Rapp F

出版信息

J Gen Virol. 1982 May;60(Pt 1):15-24. doi: 10.1099/0022-1317-60-1-15.

Abstract

Previous studies in this laboratory have quantified the fibrinolytic activity of herpesvirus-transformed cell lines and implicated the proteolytic capacity of cloned cell lines in the formation of primary and metastatic tumours. Because of the involvement of proteases in tumourigenesis in this system, we examined the effect of various protease inhibitors (alpha-1-antitrypsin, leupeptin and alpha-2-macroglobulin), as well as hamster serum containing acute phase proteins generated in response to physiological trauma, on the fibrinolytic capacity of a herpes simplex virus type 2-transformed hamster cell line. The effects of the various inhibitors on cell growth, fibrinolysis in vitro and tumourigenesis were examined. Leupeptin, alpha-1-antitrypsin, alpha-2-macroglobulin and hamster serum containing acute phase proteins were capable of inhibiting fibrinolysis in vitro, were not toxic to the cells and their action was reversible, while rejection of a mixture of protease inhibitor and transformed cells resulted in delayed tumour development.

摘要

本实验室先前的研究已对疱疹病毒转化细胞系的纤溶活性进行了定量,并表明克隆细胞系的蛋白水解能力与原发性和转移性肿瘤的形成有关。由于蛋白酶参与了该系统中的肿瘤发生过程,我们研究了各种蛋白酶抑制剂(α-1-抗胰蛋白酶、亮抑酶肽和α-2-巨球蛋白)以及含有因生理创伤而产生的急性期蛋白的仓鼠血清对单纯疱疹病毒2型转化的仓鼠细胞系纤溶能力的影响。研究了各种抑制剂对细胞生长、体外纤溶作用和肿瘤发生的影响。亮抑酶肽、α-1-抗胰蛋白酶、α-2-巨球蛋白以及含有急性期蛋白的仓鼠血清能够在体外抑制纤溶作用,对细胞无毒且其作用是可逆的,而排斥蛋白酶抑制剂与转化细胞的混合物会导致肿瘤发展延迟。

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