Morita T
Tsukuba Research Laboratories, Nippon Glaxo Ltd., Ibaraki, Japan.
Mutat Res. 1995 Jun;334(3):301-8. doi: 10.1016/0165-1161(95)90067-5.
The effect of low pH on sister-chromatid exchanges (SCE), chromosomal aberrations (CA), and the cell cycle were investigated in Chinese hamster cells. The cells were treated in media over the pH range 7.2-5.4 during 24-h continuous or 3-h pulse treatments. In Chinese hamster ovary K1 cells, slight increases in SCE frequency were induced by 3-h pulse treatment with a 28-h recovery time. In Chinese hamster V79 379A cells, similar slight increases in SCE frequency were observed with both treatments. A severe delay in the cell cycle was noted in both cell types. DNA analysis with flow cytometry indicated that the cell cycle delay occurred in S phase. CA were observed in the first metaphase. Multiple fixation times over a 27-h period were used to determine whether or not CA could be induced in cells exposed to low pH medium in more than one part of the cell cycle. Only a few chromatid gaps were induced when the cells were fixed at 0-9 h after the 3-h treatment, most probably representing cells that were treated in their G2 or late S phase. CA were induced in cells fixed between 12 and 27 h after the 3-h treatment. These cells were most probably treated in early S phase, in G1, or in the previous G2/M. These results suggest that low pH clastogenicity is S-dependent.
研究了低pH值对中国仓鼠细胞姐妹染色单体交换(SCE)、染色体畸变(CA)及细胞周期的影响。在24小时连续处理或3小时脉冲处理期间,将细胞置于pH值范围为7.2至5.4的培养基中。在中国仓鼠卵巢K1细胞中,经3小时脉冲处理并恢复28小时后,SCE频率略有增加。在中国仓鼠V79 379A细胞中,两种处理方式均观察到SCE频率有类似的轻微增加。两种细胞类型均出现了严重的细胞周期延迟。流式细胞术DNA分析表明,细胞周期延迟发生在S期。在第一次中期观察到染色体畸变。在27小时内采用多个固定时间来确定在细胞周期的多个阶段暴露于低pH培养基中的细胞是否能诱导产生染色体畸变。在3小时处理后0至9小时固定细胞时,仅诱导出少数染色单体裂隙,很可能代表在G2期或S期晚期接受处理的细胞。在3小时处理后12至27小时固定的细胞中诱导出了染色体畸变。这些细胞很可能是在S期早期、G1期或前一个G2/M期接受处理的。这些结果表明,低pH致断裂性是依赖于S期的。