van Delft J H, Baan R A
Department of Genetic Toxicology, TNO Nutrition and Food Research Institute, Rijswijk, The Netherlands.
Mutagenesis. 1995 May;10(3):209-14. doi: 10.1093/mutage/10.3.209.
Germ cell mutagenesis was studied in male lambda lacZ transgenic mice in such a way that the data can be compared with literature data for germ cell mutagenesis obtained with the specific-locus test. This comparison is of interest for validation of the transgenic mouse model. We studied mutagenesis induced by ethylnitrosourea (ENU) in mature spermatozoa isolated from epididymis and vas deferens. In order to investigate mutagenesis in different phases of spermatogenesis, animals were killed at various time points after treatment. After an ENU dose of 150 mg/kg, an increase of the mutant frequency (MF) occurred only in stem cells (9-fold; 100 days post-treatment) but not in post-stem cells (0.1 and 7 days post-treatment). Specific locus test data from literature showed a larger induction of mutations in stem cells (44-fold; > 42 days post-treatment). Although spermatogenesis in mice normally takes approximately 42 days, we found only a limited increase of the MF at 50 days post-treatment. This may be due to a delay of spermatogenesis, which was confirmed by the observation that O6-ethylguanine levels in spermatozoan DNA remained approximately the same between 0.1 and 50 days and were reduced to background levels at 100 days. Dose-response studies with the lambda lacZ mice indicated a threshold for mutation induction in stem cells at low ENU dosages, which is in accordance with the specific-locus test data. In summary, our experiments suggest that lambda lacZ transgenic mice are a suitable model to study germ cell mutagenesis in spermatogonial stem cells.
在雄性λ-乳糖操纵子转基因小鼠中研究了生殖细胞诱变,以便能够将数据与通过特定位点试验获得的生殖细胞诱变文献数据进行比较。这种比较对于转基因小鼠模型的验证具有重要意义。我们研究了从附睾和输精管分离的成熟精子中乙基亚硝基脲(ENU)诱导的诱变。为了研究精子发生不同阶段的诱变情况,在处理后的不同时间点处死动物。给予150mg/kg的ENU剂量后,仅在干细胞中突变频率(MF)增加(9倍;处理后100天),而在干细胞后阶段(处理后0.1天和7天)未增加。文献中的特定位点试验数据显示干细胞中的突变诱导作用更大(44倍;处理后>42天)。虽然小鼠的精子发生通常需要约42天,但我们发现在处理后50天MF仅有限增加。这可能是由于精子发生延迟,这一点通过观察精子DNA中的O6-乙基鸟嘌呤水平在0.1天至50天之间保持大致相同且在100天时降至背景水平得到证实。对λ-乳糖操纵子小鼠的剂量反应研究表明,在低ENU剂量下干细胞中存在突变诱导阈值,这与特定位点试验数据一致。总之,我们的实验表明,λ-乳糖操纵子转基因小鼠是研究精原干细胞中生殖细胞诱变的合适模型。