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汇合培养时间对人二倍体成纤维细胞紫外线诱变的影响。

Influence of confluent holding time on UV light mutagenesis in human diploid fibroblasts.

作者信息

Grosovsky A J, Little J B

出版信息

Mutat Res. 1983 Aug;110(2):401-12. doi: 10.1016/0027-5107(83)90156-2.

Abstract

We have investigated the induction of mutants resistant to 6-thioguanine (6TG) following 254 nm ultraviolet light exposure of density-inhibited cultures of human diploid fibroblasts. Phenotypic expression of 6TG resistance was maximal within 9 days and remained stable through 19 days after irradiation. In reconstruction studies, complete recovery of 6TG-resistant mutants occurred at cell densities of up to 35 000 cells per 100-mm petri dish. The induced mutation frequency increased linearly with dose over the range of 3-9 J/m2; the D0 of the survival curve was 4.2 J/m2. Delaying subculture to low density for 1.5-24 h after irradiation produced unexpected alterations in induced mutation frequencies. An increase in UV-induced mutations of approximately 3-fold was observed in cultures maintained in confluence for 3 h. This trend was reversed with longer holding times: the mutation frequency declined sharply in cultures held for 6 h as compared to the 3-h value, and thereafter showed a steady and gradual diminution to background levels. These data suggest that the repair of potentially mutagenic damage is a complex phenomenon which can lead to an increase or decrease in mutation frequency as a function of holding time. Although the decline in mutation frequency observed following longer holding intervals is consistent with the notion of an error-free process, we hypothesize that the increased mutation frequency produced by a short holding period reflects the existence of a cell-mediated process which enhances the mutagenic potential of at least some UV-induced DNA photoproducts.

摘要

我们研究了人二倍体成纤维细胞密度抑制培养物经254nm紫外线照射后对6-硫鸟嘌呤(6TG)耐药突变体的诱导情况。6TG耐药性的表型表达在照射后9天内达到最大值,并在19天内保持稳定。在重建研究中,每100mm培养皿中细胞密度高达35000个细胞时,6TG耐药突变体可完全恢复。在3-9J/m2的剂量范围内,诱导突变频率随剂量呈线性增加;存活曲线的D0为4.2J/m2。照射后将传代培养推迟至低密度状态1.5-24小时,会使诱导突变频率发生意外变化。在汇合状态下维持3小时的培养物中,紫外线诱导的突变增加了约3倍。随着保持时间延长,这种趋势发生逆转:与3小时的值相比,保持6小时的培养物中突变频率急剧下降,此后逐渐稳定下降至背景水平。这些数据表明,潜在诱变损伤的修复是一个复杂的现象,它可能导致突变频率随保持时间的变化而增加或减少。尽管在较长保持间隔后观察到的突变频率下降与无差错过程的概念一致,但我们推测,短时间保持导致的突变频率增加反映了一种细胞介导过程的存在,该过程增强了至少一些紫外线诱导的DNA光产物的诱变潜力。

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