van Rijn J, van den Berg J, van Meeteren A, van Wijk R
Radiat Res. 1983 Aug;95(2):262-72.
Reuber H35 rat hepatoma cells, clone KRC, were used to study the effect of cyclic AMP on radiation-induced cell death. Treatment of logarithmically growing cultures with 0.5 mM cAMP for 17 hr prior to irradiation resulted in a decreased cell survival. Similar results were obtained with cultures irradiated after treatment with Bt2cAMP. Treatment of H35 cells with cAMP or Bt2cAMP caused inhibition of their proliferation and resulted in an accumulation of cells in early S phase and a depletion of G2-phase cells. In synchronized cultures cells were relatively radioresistant during their S phase. In addition to single-dose treatment with X rays, the effect of Bt2cAMP on radiation-induced cell death was studied during fractionated irradiation with 2.5 Gy per day. This fractionated irradiation resulted in a dose-reduction factor of 1.6 at the 10% survival level and a 10-fold decrease in the surviving cell population due to the cooperative effects of Bt2cAMP on growth rate and radiation survival. The effect of cAMP on radiation-induced mitotic delay was also studied. It appeared that whereas cAMP had no effect on the progression of G2 cells into mitosis, it prevented cells from recovery from the X-ray mitotic delay in G2.
使用Reuber H35大鼠肝癌细胞系KRC克隆来研究环磷酸腺苷(cAMP)对辐射诱导细胞死亡的影响。在照射前,用0.5 mM cAMP处理对数生长期的细胞培养物17小时,导致细胞存活率降低。用双丁酰环磷腺苷(Bt2cAMP)处理后再进行照射的培养物也得到了类似结果。用cAMP或Bt2cAMP处理H35细胞会抑制其增殖,并导致细胞在S期早期积累,G2期细胞减少。在同步培养物中,细胞在S期相对抗辐射。除了用X射线进行单剂量处理外,还研究了Bt2cAMP在每天2.5 Gy分次照射期间对辐射诱导细胞死亡的影响。这种分次照射在10%存活水平时导致剂量减少因子为1.6,由于Bt2cAMP对生长速率和辐射存活的协同作用,存活细胞群体减少了10倍。还研究了cAMP对辐射诱导的有丝分裂延迟的影响。结果表明,虽然cAMP对G2期细胞进入有丝分裂的进程没有影响,但它阻止细胞从G2期的X射线有丝分裂延迟中恢复。