Generoso W M, Cain K T, Cornett C V, Frome E L
Biology Division, Oak Ridge National Laboratory, TN 37731-8077.
Mutat Res. 1991 Aug;249(2):301-10. doi: 10.1016/0027-5107(91)90004-8.
In a previous report (Generoso et al., 1985) it was shown that the two hybrid stocks of mice, (C3H/R1 x 101/R1)F1 and (SEC/R1 x C57BL/6)F1, differed in their responses to induction of chromosomal aberrations following exposure of the stem-cell spermatogonia to 500 R x 4 (4-week intervals) acute X-rays. The levels of response in the two stocks were paralleled by the effects on the length of the sterile period, which presumably results from stem-cell killing and repopulation. The present study was conducted in order to determine whether the differences between the two stocks in these parameters hold true also for other conditions of radiation exposure. Thus, comparative experiments were conducted using the following acute exposure regimens: 500 R single dose, 500 R + 500 R (24-h interval), 100 R + 900 R (24-h interval), and 500 R x 4 (8-week intervals). The endpoints measured were chromosome rearrangements in diakinesis/metaphase-I meiocytes, embryonic lethality in conceptuses, length of sterile period and testis weight. Trend analysis indicated that higher frequencies of chromosome rearrangements and embryonic lethality were recovered from (C3H/R1 x 101/R1)F1 than from (SEC/R1 x C57BL/6)F1 males, that there were no significant differences between stocks in testis weight reductions, and that there was no consistency in the direction of the significant differences that occurred in the length of the sterile period. A definitive conclusion regarding the possible association between induction of chromosomal aberrations and induction of cell killing awaits direct histological analysis of the stem-cell population.
在之前的一份报告中(杰内罗索等人,1985年)表明,两种小鼠杂交品系,即(C3H/R1×101/R1)F1和(SEC/R1×C57BL/6)F1,在其干细胞精原细胞暴露于500伦琴×4(间隔4周)的急性X射线后,对染色体畸变诱导的反应有所不同。这两种品系的反应水平与对不育期长度的影响平行,不育期长度的影响可能是由于干细胞的杀伤和再增殖导致的。进行本研究是为了确定这两种品系在这些参数上的差异在其他辐射暴露条件下是否也成立。因此,使用以下急性暴露方案进行了比较实验:500伦琴单剂量、500伦琴+500伦琴(间隔24小时)、100伦琴+900伦琴(间隔24小时)以及500伦琴×4(间隔8周)。所测量的终点指标包括终变期/减数分裂中期I的减数分裂细胞中的染色体重排、着床前胚胎的致死率、不育期长度和睾丸重量。趋势分析表明,从(C3H/R1×101/R1)F1雄性小鼠中回收的染色体重排和胚胎致死率的频率高于(SEC/R1×C57BL/6)F1雄性小鼠,两种品系在睾丸重量减轻方面没有显著差异,并且在不育期长度出现的显著差异方向上没有一致性。关于染色体畸变诱导与细胞杀伤诱导之间可能关联的明确结论有待对干细胞群体进行直接组织学分析。