Wolff L, Tambourin P, Ruscetti S
Virology. 1986 Jul 15;152(1):272-6. doi: 10.1016/0042-6822(86)90393-4.
The erythroleukemia induced by the Friend spleen focus-forming virus (SFFV) in mice exemplifies a multistep oncogenic process. Its sequential steps include a rapid polyclonal hyperplastic stage and a more slowly developing malignant stage characterized by autonomous erythroid cells. We report here that the helper virus normally present in mice infected by SFFV is not required for development of the second stage of transformation. In this study, mice were infected with a polycythemia-inducing variant of SFFV which was prepared as a helper-free stock (L. Wolff and S. Ruscetti, 1985, Science 228, 1549). Highly malignant cells could be detected in helper-free SFFV-infected mice by their transplantability into the omentum of sublethally irradiated mice, and erythroleukemia cell lines, typical of previously isolated Friend murine erythroleukemia cell lines, could be established from diseased spleens. Like their helper virus-containing counterparts, the lines established with helper-free SFFV are inducible for hemoglobin synthesis with a variety of chemicals, but not erythropoietin, and express p53, a marker of malignant transformation. Although the cells expressed SFFV encoded proteins, none expressed gene products of replication competent murine leukemia viruses.
由弗瑞德脾集落形成病毒(SFFV)诱导的小鼠红白血病是多步骤致癌过程的一个例证。其连续步骤包括一个快速的多克隆增生阶段和一个以自主性红系细胞为特征的发展较为缓慢的恶性阶段。我们在此报告,被SFFV感染的小鼠中正常存在的辅助病毒对于转化的第二阶段发展并非必需。在本研究中,用一种诱导红细胞增多症的SFFV变异体感染小鼠,该变异体被制备成无辅助病毒的毒株(L. 沃尔夫和S. 鲁斯凯蒂,1985年,《科学》228卷,1549页)。通过将无辅助病毒的SFFV感染小鼠的细胞移植到经亚致死剂量照射的小鼠的网膜中,可检测到高度恶性的细胞,并且可从患病脾脏中建立起典型的先前分离的弗瑞德小鼠红白血病细胞系的红白血病细胞系。与含有辅助病毒的对应细胞系一样,用无辅助病毒的SFFV建立的细胞系可被多种化学物质诱导合成血红蛋白,但不能被促红细胞生成素诱导,并且表达p53,这是恶性转化的一个标志物。尽管这些细胞表达SFFV编码的蛋白,但没有一个表达具有复制能力的鼠白血病病毒的基因产物。