Evans H J
Mutat Res. 1984 Jan;125(1):87-94. doi: 10.1016/0027-5107(84)90035-6.
Lymphocytes separated from human peripheral blood were cultured in vitro, in the presence of 6-thioguanine (TG), to select and clone rare TG-resistant (TGr) cells present in the circulation in vivo. The incidence of such TGr cells ranged from 0.83 X 10(-5) to 2.53 X 10(-5) (mean 1.48 X 10(-5) ) in healthy individuals aged between 19 and 79 years; did not differ between males and females; but increased significantly with age at a rate of 2.4 cells/10(7) lymphocytes/year. Exposure of lymphocytes (G0) in vitro to X-ray doses of upto 200 rad resulted in a dose-dependent increase in TGr cell frequencies. The rates of increase were approximately in proportion to the square of the dose and these rates were closely similar to those obtained in cultured skin fibroblasts and suggest that the bulk of these mutations are a consequence of chromosome structural aberrations. The cloned TGr cells are considered to be HPRT- mutants and the mutation frequencies in lymphocytes determined using this cloning technique were compared with the variant frequencies obtained in earlier experiments utilising an autoradiographic technique to detect azaguanine-resistant (AGr) variant cells. Mutation frequencies with the cloning technique were 10-20-fold lower than variant frequencies with the autoradiographic method.
从人外周血中分离出的淋巴细胞在体外培养,同时加入6-硫鸟嘌呤(TG),以筛选并克隆体内循环中存在的罕见的TG抗性(TGr)细胞。在19至79岁的健康个体中,此类TGr细胞的发生率在0.83×10⁻⁵至2.53×10⁻⁵之间(平均为1.48×10⁻⁵);男女之间无差异;但随年龄显著增加,增加速率为每年2.4个细胞/10⁷淋巴细胞。体外将淋巴细胞(G0期)暴露于高达200拉德的X射线剂量下,会导致TGr细胞频率呈剂量依赖性增加。增加速率大致与剂量的平方成正比,且这些速率与培养的皮肤成纤维细胞中获得的速率非常相似,这表明这些突变大部分是染色体结构畸变的结果。克隆的TGr细胞被认为是次黄嘌呤磷酸核糖转移酶(HPRT)突变体,将使用这种克隆技术测定的淋巴细胞中的突变频率与早期利用放射自显影技术检测抗氮杂鸟嘌呤(AGr)变异细胞的实验中获得的变异频率进行了比较。克隆技术的突变频率比放射自显影方法的变异频率低10至20倍。