Muakkassah-Kelly S F, Jans D A, Lydon N, Bieri F, Waechter F, Bentley P, Stäubli W
Central Toxicology Unit, Ciba-Geigy Limited, Basel, Switzerland.
Exp Cell Res. 1988 Oct;178(2):296-306. doi: 10.1016/0014-4827(88)90400-4.
The human c-myc gene was introduced and transiently expressed in adult rat hepatocyte cultures by the technique of electroporation and its effect on DNA synthesis was examined. Epidermal growth factor (EGF) has been found to stimulate a wave of DNA synthesis in electroporated rat hepatocytes. Hepatocyte cultures electroporated with the c-myc gene showed a potentiation of this EGF effect exhibiting rates of DNA synthesis up to 50% greater than those of control electroporated cultures, as determined by [3H]thymidine labeling of cell nuclei. This potentiation was dependent on the amount of c-myc DNA transfected. The potentiation was due neither to an alteration in the dose-response of the stimulatory effect of EGF nor to a change in the time course of the DNA synthesis wave.
通过电穿孔技术将人类c-myc基因导入成年大鼠肝细胞培养物中并使其瞬时表达,然后检测其对DNA合成的影响。已发现表皮生长因子(EGF)能刺激电穿孔大鼠肝细胞中的一波DNA合成。用c-myc基因进行电穿孔的肝细胞培养物显示出这种EGF效应的增强,通过细胞核的[3H]胸腺嘧啶核苷标记测定,其DNA合成速率比对照电穿孔培养物高50%。这种增强依赖于转染的c-myc DNA的量。这种增强既不是由于EGF刺激作用的剂量反应改变,也不是由于DNA合成波的时间进程变化。