Bergholz C M, Wolfe L G, Deinhardt F
Int J Cancer. 1977 Jul 15;20(1):104-11. doi: 10.1002/ijc.2910200117.
Simian sarcoma virus, type 1 (SSV-1)-transformed non-producer cell lines were established by infection of normal marmoset fibroblast cells (HF) with limiting dilutions of SSV-1. Four focus-derived cell lines were identified as non-producers by assay of culture fluids for focus-forming activity and by the mixed culture cytopathogenicity test with XC cells. Further studies failed to detect production of type-C virus by 3H-uridine labelling, reverse transcriptase assay or electron microscopy. The non-producer cell lines, designated HF/SSV-NPI, IV, V, and VI, appeared morphologically transformed and cloned in soft agar with the same efficiency as HF/SSV-1 virus-producing transformed cells. Expression of either cytoplasmic or cell surface virus-related antigens was not detected by immunofluorescence or serum cytotoxicity tests. The presence of sarcoma genome in the transformed non-producer cell lines was demonstrated by rescue of focus-forming activity following superinfection with non-transforming helper virus or by cocultivation with helper-virus-producing cell lines. The SSV-1-transformed non-producer primate cells provide a useful tool for future studies.
通过用有限稀释的猿猴肉瘤病毒1型(SSV-1)感染正常狨猴成纤维细胞(HF),建立了SSV-1转化的非生产性细胞系。通过检测培养液的集落形成活性以及与XC细胞进行混合培养细胞病变效应试验,鉴定出四个源自集落的细胞系为非生产性细胞系。进一步研究未能通过3H-尿苷标记、逆转录酶测定或电子显微镜检测到C型病毒的产生。这些非生产性细胞系命名为HF/SSV-NPI、IV、V和VI,在形态上呈现转化特征,并且在软琼脂中克隆的效率与产生HF/SSV-1病毒的转化细胞相同。通过免疫荧光或血清细胞毒性试验未检测到细胞质或细胞表面病毒相关抗原的表达。在用非转化辅助病毒超感染后集落形成活性的恢复,或与产生辅助病毒的细胞系共培养,证明了转化的非生产性细胞系中肉瘤基因组的存在。SSV-1转化的非生产性灵长类细胞为未来的研究提供了一个有用的工具。