Coppola J A, Cole M D
Nature. 1986;320(6064):760-3. doi: 10.1038/320760a0.
Mouse erythroleukaemia cells (also called Friend cells) can be isolated from the spleen of certain strains of mice that have been infected with the Friend virus complex. The cells resemble proerythroblasts and, when exposed to dimethyl sulphoxide (DMSO) or a variety of other chemicals, can be induced to undergo a programme of differentiation which closely resembles the final stages of normal erythropoiesis. This includes the cessation of proliferation and large increases in the production of messenger RNA for both alpha- and beta-globin. In addition, DMSO induces a rapid (less than 2 h) decrease in c-myc mRNA levels. The c-myc oncogene is expressed in the majority of proliferating normal cells and altered expression of the gene has been implicated in the genesis of a wide variety of tumours. To study the influence of oncogene activation on differentiation, we have transfected viral-promoter-driven c-myc genes into mouse erythroleukaemia cells. Constitutive c-myc expression was found to block DMSO-induced differentiation.
小鼠红白血病细胞(也称为弗瑞德细胞)可从感染了弗瑞德病毒复合体的某些品系小鼠的脾脏中分离得到。这些细胞类似于早幼红细胞,当暴露于二甲基亚砜(DMSO)或多种其他化学物质时,可被诱导经历一个分化程序,该程序与正常红细胞生成的最后阶段非常相似。这包括增殖停止以及α-和β-珠蛋白信使RNA产量大幅增加。此外,DMSO可诱导c-myc mRNA水平迅速(少于2小时)下降。c-myc癌基因在大多数增殖的正常细胞中表达,该基因表达的改变与多种肿瘤的发生有关。为了研究癌基因激活对分化的影响,我们已将病毒启动子驱动的c-myc基因转染到小鼠红白血病细胞中。发现组成型c-myc表达会阻断DMSO诱导的分化。