Nishi Y, Hasegawa M M, Inui N
Toxicol Lett. 1983 Jul;17(3-4):335-42. doi: 10.1016/0378-4274(83)90247-3.
Studies were made on chromosome aberrations in Syrian hamster embryonal fibroblasts (SHEF) at early and late passages in culture. Aberrations were induced with a potent indirect clastogen, 7,12-dimethylbenz(a)anthracene (DMBA). Results showed that cells at late passages were much more susceptible to this chemical than cells at early passages: the frequency of aberrant metaphases was usually less than 20% at the 2nd passage, but it gradually increased with increase in the number of culture passages, reaching 50% or more at the 8th passage in one experiment and 6th-7th passage in another. Induction of chromosome aberrations was also examined in V79 cells co-cultured with hamster cells at early and late passages. V79 cells are known to have no drug-metabolizing enzyme activity. Results demonstrate that the frequency of chromosome aberrations of V79 cells was much greater in the presence of hamster cells at late passages than in the presence of cells at early passages.
对叙利亚仓鼠胚胎成纤维细胞(SHEF)在培养早期和晚期传代时的染色体畸变进行了研究。用一种强效间接致裂剂7,12 - 二甲基苯并(a)蒽(DMBA)诱导畸变。结果表明,晚期传代的细胞比早期传代的细胞对这种化学物质更敏感:在第2代时异常中期的频率通常低于20%,但随着培养代数的增加逐渐升高,在一次实验中第8代时达到50%或更高,在另一次实验中第6 - 7代时达到50%或更高。还在与早期和晚期传代的仓鼠细胞共培养的V79细胞中检测了染色体畸变的诱导情况。已知V79细胞没有药物代谢酶活性。结果表明,在晚期传代的仓鼠细胞存在的情况下,V79细胞的染色体畸变频率比在早期传代的细胞存在的情况下要高得多。