Laval F
Biochimie. 1985 Mar-Apr;67(3-4):361-4. doi: 10.1016/s0300-9084(85)80081-x.
Pretreatment of H4 (rat hepatoma) cells for 48 h with non toxic doses of alkylating agents methylmethane sulfonate, (MMS), N-methyl-N'-nitro-N-nitrosoguanidine (MNNG) renders the cells more resistant to the toxic and mutagenic effects of these compounds. This adaptive response seems to reflect improved repair of methylated lesions in cellular DNA. Therefore, we measured the activity of the DNA-glycosylase for N-methylated purines (7-MeGua and 3-MeAd) and the activity of the O6-methylguanine-DNA methyltransferase in control and adapted cells. We show that the adaptive response does not significantly increase the DNA-glycosylase activity but involves the induction of methyltransferase molecules.
用无毒剂量的烷化剂甲磺酸甲酯(MMS)、N-甲基-N'-硝基-N-亚硝基胍(MNNG)对H4(大鼠肝癌)细胞进行48小时预处理,可使细胞对这些化合物的毒性和诱变作用产生更强的抗性。这种适应性反应似乎反映了细胞DNA中甲基化损伤修复能力的提高。因此,我们测定了对照细胞和适应细胞中针对N-甲基化嘌呤(7-甲基鸟嘌呤和3-甲基腺嘌呤)的DNA糖基化酶活性以及O6-甲基鸟嘌呤-DNA甲基转移酶的活性。我们发现,适应性反应并没有显著提高DNA糖基化酶的活性,但涉及甲基转移酶分子的诱导。