Knightbridge A, Ralph R K
Mol Cell Biochem. 1981 Feb 11;34(3):153-64. doi: 10.1007/BF02359620.
Addition of N6,O2'-Dibutyryladenosine cyclic 3',5'-monophosphate (DB cyclic AMP) plus theophylline or transfer to medium containing 0.2% serum slowed the growth of cultured mouse mastocytoma cells and eventually arrested their growth in G1 phase. Examination of the properties of cells arrested by either procedure suggested that the drugs arrested cells in G1 phase 1.5-2 h after the point of low serum arrest. Cycloheximide prevented the recovery of cell growth after low serum or drug-induced arrest demonstrating that protein synthesis was necessary to pass either growth restriction point. Cordycepin also prevented drug-arrested cells from progressing into cycle indicating a requirement for RNA synthesis to overcome the drug-induced growth arrest. Evidence is also presented that DB cyclic AMP prevented the cells receiving a pulse of calcium necessary to proceed past the DB cyclic AMP-sensitive growth restriction point. It is suggested that high cyclic AMP levels prevent mastocytoma cells from receiving a surge of calcium in G1 phase that is necessary if the cells are to proceed to S phase and eventually divide.
添加 N6,O2'-二丁酰腺苷 3',5'-环磷酸酯(DB 环磷腺苷)加茶碱,或转移至含 0.2%血清的培养基中,会减缓培养的小鼠肥大细胞瘤细胞的生长,并最终使其生长停滞在 G1 期。对通过上述任一方法停滞生长的细胞特性进行检测表明,这些药物会在血清含量降低导致细胞停滞生长后的 1.5 - 2 小时,使细胞停滞在 G1 期。放线菌酮可阻止血清含量降低或药物诱导导致的细胞生长停滞之后的细胞生长恢复,这表明蛋白质合成对于通过任一生长限制点都是必需的。虫草素也可阻止药物诱导停滞生长的细胞进入细胞周期,这表明克服药物诱导的生长停滞需要 RNA 合成。还有证据表明,DB 环磷腺苷可阻止细胞接收通过 DB 环磷腺苷敏感生长限制点所需的钙脉冲。有人提出,高环磷腺苷水平可阻止肥大细胞瘤细胞在 G1 期接收钙激增,而如果细胞要进入 S 期并最终分裂,这种钙激增是必需的。