Fischer-Fantuzzi L, Marin G, Vesco C
Eur J Biochem. 1975 Dec 15;60(2):505-11. doi: 10.1111/j.1432-1033.1975.tb21029.x.
Resting cultures of 3T3 cells (an established line of mouse fibroblasts) were released from density inhibition by either infection with Simian virus 40 or addition of serum. The increased rate of thymidine incorporation into DNA, induced by these two agents, was measured in the presence and in the absence of three inhibitory conditions (cycloheximide or dibutyryladenosine 3':5'-monophosphate added to the medium, or lack of anchorage). The inhibition was found to be quite similar in cultures stimulated by virus or serum; under the same conditions, however, the incorporation into mitochondrial DNA was much less inhibited than that into nuclear DNA. The experiments also suggest that new protein synthesis may not be necessary, for either virus or serum, to start the inductive mechanism.
3T3细胞(一种已建立的小鼠成纤维细胞系)的静止培养物,通过感染猿猴病毒40或添加血清来解除密度抑制。在存在和不存在三种抑制条件(向培养基中添加环己酰亚胺或二丁酰腺苷3':5'-单磷酸,或缺乏锚定)的情况下,测量了这两种试剂诱导的胸苷掺入DNA的速率增加。发现病毒或血清刺激的培养物中的抑制作用非常相似;然而,在相同条件下,线粒体DNA的掺入受到的抑制远小于核DNA。实验还表明,无论是病毒还是血清,启动诱导机制可能都不需要新的蛋白质合成。