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疱疹病毒转化细胞产生纤溶酶原激活物。

Production of plasminogen activator by cells transformed by herpesviruses.

作者信息

Howett M K, High C S, Rapp F

出版信息

Cancer Res. 1978 Apr;38(4):1075-8.

PMID:205345
Abstract

Plasminogen activator is produced by hamster cells transformed by human herpesviruses. These cell lines have previously been shown to be oncogenic when injected s.c. into newborn syngeneic hamsters. Lysis of fibrin overlays by these cell lines was plasminogen dependent. Normal hamster embryo fibroblasts and a hamster cell line transformed by PARA-7 (an adenovirus-SV 40 hybrid) failed to produced lysis. In separate experiments fibrin overlay of lytically infected secondary rabbit kidney cells did not show induction of this activity during the normal course of productive infection. The human cell line TE-85 clone F-5, a clonal cell line from a human osteogenic sarcoma, failed to produce plasminogen activator, but two separate clones of these cells that were morphologically transformed after exposure to UV-inactivated herpes simplex virus type 2 produced rapid lysis of the fibrin overlay. Clonal variation was observed in herpes simplex virus types 1 and 2-transformed hamster lines and is under investigation. It is suggested that plasminogen activator detection may serve as a convenient assay system for transformation of normal cells by herpesviruses.

摘要

纤溶酶原激活物由人疱疹病毒转化的仓鼠细胞产生。这些细胞系先前已被证明,当皮下注射到同基因新生仓鼠体内时具有致癌性。这些细胞系对纤维蛋白覆盖物的溶解作用依赖于纤溶酶原。正常仓鼠胚胎成纤维细胞和由PARA - 7(一种腺病毒 - SV40杂种病毒)转化的仓鼠细胞系未能产生溶解作用。在单独的实验中,在生产性感染的正常过程中,被裂解感染的二代兔肾细胞的纤维蛋白覆盖物未显示出这种活性的诱导。人成骨肉瘤的克隆细胞系TE - 85克隆F - 5未能产生纤溶酶原激活物,但这些细胞的两个单独克隆在暴露于紫外线灭活的2型单纯疱疹病毒后发生形态转化,能快速溶解纤维蛋白覆盖物。在1型和2型单纯疱疹病毒转化的仓鼠细胞系中观察到克隆变异,正在对此进行研究。有人提出,纤溶酶原激活物检测可能作为一种方便的检测系统,用于检测疱疹病毒对正常细胞的转化。

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