Shay J W, Wright W E
Department of Cell Biology, University of Texas, Southwestern Medical Center, Dallas 75235.
Exp Cell Res. 1989 Sep;184(1):109-18. doi: 10.1016/0014-4827(89)90369-8.
The mechanism by which SV40 large T-antigen immortalizes human lung fibroblasts is not yet understood, and the frequency with which immortalization occurs is unknown. Here we report detailed studies of the kinetics of immortalization. Approximately 20-50% of individual T-antigen transfected clones of IMR-90 human lung fibroblasts are able to immortalize. The failure of some clones to immortalize is consistent with the hypothesis that in some cells the aneuploidy induced by T-antigen produces extra copies of the chromosome containing a factor that must be inactivated before immortalization occurs. Within immortalization-competent clones, the frequency of immortalization is about 3 X 10(-7). This frequency is consistent with a mutational mechanism for the inactivation of the factor that causes crisis in T-antigen expressing cells.
猿猴病毒40(SV40)大T抗原使人类肺成纤维细胞永生化的机制尚不清楚,永生化发生的频率也未知。在此,我们报告了关于永生化动力学的详细研究。IMR - 90人类肺成纤维细胞中,约20 - 50%的单个T抗原转染克隆能够实现永生化。一些克隆未能永生化,这与以下假设一致:在某些细胞中,T抗原诱导的非整倍体产生了含有一个因子的染色体的额外拷贝,该因子在永生化发生之前必须被灭活。在具有永生化能力的克隆中,永生化频率约为3×10^(-7)。这个频率与导致表达T抗原的细胞出现危机的因子失活的突变机制相符。