Surmacz E, Kaczmarek L, Rønning O, Baserga R
Mol Cell Biol. 1987 Feb;7(2):657-63. doi: 10.1128/mcb.7.2.657-663.1987.
We constructed a stable cell line, 3T3A5, which carried a chimeric gene in which the simian virus 40 T-antigen-coding gene was under the control of the mouse ribosomal DNA promoter. These cells expressed T antigen when they were growing exponentially in 10% fetal calf serum, but they all became T negative when incubated for 5 days in low-concentration serum. The readdition of serum or platelet-poor plasma again induced the expression of T antigen, which was accompanied by an increase in steady-state levels of the corresponding RNA. Among the various growth factors tested for their ability to induce T-antigen expression in 3T3A5 cells, only insulinlike growth factor I (IGF-I) could induce T antigen at physiological concentrations. The effect of IGF-I or platelet-poor plasma was abolished by an antibody to IGF-I. Other growth factors, like insulin and epidermal growth factor, could induce the expression of T antigen in 3T3A5 cells, but only at concentrations far above the physiological range. Other growth factors were totally ineffective. These results indicate that exposure of cells to IGF-I can activate transcription from the ribosomal DNA promoter.
我们构建了一个稳定的细胞系3T3A5,它携带一个嵌合基因,其中猿猴病毒40 T抗原编码基因受小鼠核糖体DNA启动子的控制。这些细胞在含有10%胎牛血清的培养基中指数生长时表达T抗原,但在低浓度血清中培养5天后全部变为T阴性。重新添加血清或贫血小板血浆可再次诱导T抗原的表达,同时相应RNA的稳态水平增加。在测试的各种生长因子中,只有胰岛素样生长因子I(IGF-I)在生理浓度下能诱导3T3A5细胞表达T抗原。IGF-I抗体可消除IGF-I或贫血小板血浆的作用。其他生长因子,如胰岛素和表皮生长因子,虽能诱导3T3A5细胞表达T抗原,但仅在远高于生理范围的浓度下才行。其他生长因子则完全无效。这些结果表明,细胞暴露于IGF-I可激活核糖体DNA启动子的转录。