Tsuyama N, Miura M, Kitahira M, Ishibashi S, Ide T
Department of Cellular and Molecular Biology, Hiroshima University School of Medicine, Japan.
Cell Struct Funct. 1991 Feb;16(1):55-62. doi: 10.1247/csf.16.55.
Two lines of immortal human fibroblasts were isolated following transfection of TIG-3 cells with plasmid DNA, pMT-1ODtsA, that contained SV40 early gene with a deletion in replication origin and ts mutation in coding sequence for T-antigen. These cells continued proliferation at 34 degrees C, over 565 population doubling level (PDL) which is far over the limited division potential of untransformed normal TIG-3 of 70-80 PDL. When the culture temperature was shifted to 40 degrees C after 70 PDL, they ceased proliferation immediately. One of these immortal clones, SVts8, lost its ts phenotype after retransformation with wtT-antigen gene. These results indicated that the function of intact T-antigen is required for maintenance of immortal proliferation, at least in one of the SV40 transformed immortal clones.
用含有SV40早期基因的质粒DNA(pMT-1ODtsA)转染TIG-3细胞后,分离出两株永生的人成纤维细胞系。该质粒DNA的复制起点有缺失,T抗原编码序列存在温度敏感突变。这些细胞在34℃下持续增殖,超过了565个群体倍增水平(PDL),这远远超过了未转化的正常TIG-3细胞70 - 80 PDL的有限分裂潜能。当培养温度在70个PDL后转移到40℃时,它们立即停止增殖。其中一个永生克隆SVts8在用野生型T抗原基因再次转化后失去了温度敏感表型。这些结果表明,完整的T抗原功能对于维持永生增殖是必需的,至少在其中一个SV40转化的永生克隆中是如此。