Shibuya T, Murota T, Horiya N, Matsuda H, Hara T
Laboratory of Genetic Toxicology, Hatano Research Institute, Kanagawa, Japan.
Mutat Res. 1993 Dec;290(2):273-80. doi: 10.1016/0027-5107(93)90168-f.
A specific-locus test was carried out to examine the mutagenic activity of N-ethyl-N-nitrosourea (ENU) on mouse primordial germ cells (PGC). Embryos of C3H/He mice were treated transplacentally with 30 or 50 mg ENU per kg of maternal body weight on day 8.5, 10.5, or 13.5 of gestation (G8.5 day, G10.5 day, or G13.5 day). Male and female mice that had been treated with ENU in embryonic stages were mated with female or male tester PW mice to detect recessive mutations induced in PGC. ENU induced recessive mutations at a relatively high rate in PGC at these developmental stages. The most sensitive stage was G10.5 day. On G8.5 day, the induced mutation rate in males and females was not significantly different. Cluster mutations, which originate from the limited number of PGC and cell killing, were more frequently induced at an earlier developmental stage. The induced mutation rate per unit dose of ENU (1 mg/kg) was higher in G8.5 and G10.5 day PGC than in stem-cell spermatogonia. It can be concluded that mouse PGC are more sensitive than stem-cell spermatogonia to the induction of recessive mutations by ENU.
进行了一项特定位点测试,以检测N-乙基-N-亚硝基脲(ENU)对小鼠原始生殖细胞(PGC)的诱变活性。在妊娠第8.5天、10.5天或13.5天(G8.5天、G10.5天或G13.5天),给C3H/He小鼠胚胎经胎盘注射每千克母体体重30或50毫克ENU。在胚胎期接受ENU处理的雄性和雌性小鼠与雌性或雄性测试PW小鼠交配,以检测PGC中诱导的隐性突变。在这些发育阶段,ENU在PGC中诱导隐性突变的发生率相对较高。最敏感的阶段是G10.5天。在G8.5天,雄性和雌性的诱导突变率没有显著差异。起源于有限数量的PGC和细胞杀伤的簇状突变在较早的发育阶段更频繁地被诱导。G8.5和G10.5天PGC中每单位剂量ENU(1毫克/千克)的诱导突变率高于干细胞精原细胞。可以得出结论,小鼠PGC对ENU诱导隐性突变的敏感性高于干细胞精原细胞。