Epifanova O I, Rosenwald I B, Makarova G F
Institute of Molecular Biology, Academy of Sciences of the USSR, Moscow.
Acta Histochem Suppl. 1990;39:211-4.
Incubation of resting (serum-deprived) NIH 3T3 mouse fibroblasts for 12 hours with PDGF1) stimulates the onset of DNA synthesis. A brief exposure (45 minutes) of resting cells to inhibitors of protein synthesis (cycloheximide or puromycin) exerts similar effect inducing by itself the entry of cells into the S period. Incubation with EGF1) following pretreatment with either PDGF or protein synthesis inhibitors does not enhance the number of cells synthesizing DNA. The results support the assumption that the acquirement, by resting cells, of competence for DNA replication includes, as a necessary step, the down-regulation of intracellular growth inhibitors whose formation depends on protein synthesis.
将静止(血清饥饿)的NIH 3T3小鼠成纤维细胞与血小板衍生生长因子(PDGF)一起孵育12小时会刺激DNA合成的开始。将静止细胞短暂暴露(45分钟)于蛋白质合成抑制剂(放线菌酮或嘌呤霉素)会产生类似的效果,其自身诱导细胞进入S期。在用PDGF或蛋白质合成抑制剂预处理后再与表皮生长因子(EGF)一起孵育,并不会增加合成DNA的细胞数量。这些结果支持这样一种假设,即静止细胞获得DNA复制能力,作为一个必要步骤,包括下调细胞内生长抑制剂,其形成依赖于蛋白质合成。