Bempong M A
J Environ Pathol Toxicol. 1979 Jan-Feb;2(3):633-56.
Cultured chinese hamster ovary (CHO) cells were exposed to different concentrations of N-methyl-N'-nitro-N-nitrosoguanidine (MNNG) for either 24 hr or 6 days. For cytological consequences of MNNG exposure, CHO cells were treated for 24 hr and allowed a 24 hr recovery period prior to analysis; for the estimation of cytotoxicity of MNNG, cells were treated for 6 days followed by a 6 day recovery period. The cytotoxic effect of MNNG based on the colony-forming ability of treated cells showed a semi-logarithmic decrease in the number of colonies formed with an increase in MNNG concentration. The data on the cytological effect of MNNG on CHO cells demonstrate that the chemical causes both structural and numerical chromosomal anomalies and that the incidence of each aberration type is influenced by MNNG concentration. Karyomorphological analysis of CHO cells treated for 24 hr and fixed after four cell cycles showed a varied chromosome constitution ranging from 18 to 54. Chromosomal structural changes arising from breaks and/or exchanges were of chromatid types. Distribution of breaks along the length of the chromosomes and among chromosomes showed that no chromosome segment or chromosome was preferentially susceptible to the clastogenic effect of MNNG. MNNG-induced chromosomal rearrangements, such as ring configurations, exchanges, and dicentrics, exceeded such cytological errors as fragments and pulverizations. In a descending order of magnitude the induced structural rearrangements were ring chromosomes, triradials, quadriradials, and dicentrics.
将培养的中国仓鼠卵巢(CHO)细胞暴露于不同浓度的N-甲基-N'-硝基-N-亚硝基胍(MNNG)中24小时或6天。为了研究MNNG暴露的细胞学后果,将CHO细胞处理24小时,并在分析前给予24小时的恢复期;为了评估MNNG的细胞毒性,将细胞处理6天,随后给予6天的恢复期。基于处理后细胞集落形成能力的MNNG细胞毒性作用显示,随着MNNG浓度的增加,形成的集落数量呈半对数下降。关于MNNG对CHO细胞细胞学作用的数据表明,该化学物质会导致结构和数量染色体异常,并且每种畸变类型的发生率都受MNNG浓度的影响。对处理24小时并在四个细胞周期后固定的CHO细胞进行核型分析,结果显示染色体组成从18条到54条不等。由断裂和/或交换引起的染色体结构变化属于染色单体类型。沿着染色体长度和染色体之间的断裂分布表明,没有染色体片段或染色体优先易受MNNG的致断裂作用影响。MNNG诱导的染色体重排,如环状结构、交换和双着丝粒,超过了诸如片段和粉碎等细胞学错误。按数量级降序排列,诱导的结构重排依次为环状染色体、三辐射体、四辐射体和双着丝粒。