Cattanach B M, Jones C, Papworth D G
Mutat Res. 1985 Mar;149(1):105-18. doi: 10.1016/0027-5107(85)90015-6.
The specific-locus mutation frequency obtained from mouse spermatogonial stem cells following unequal, 1 + 9 Gy X-ray fractionation with a 24-h fractionation interval is low, and consistent with the two fractions acting additively. The response is therefore markedly different from the augmented mutation frequencies obtained with 500 + 500 R and 100 + 500 R, 24-h fractionations. The lower yield compared with the 100 + 500 R response also indicates a clear difference from the translocation data which demonstrate increases in yield with increasing second dose over the same dose range. The decline in specific locus mutation yield with the increase in the second dose from 500 R to 9 Gy suggests that the stem cells surviving the first fraction are heterogeneous in their sensitivities to this class of genetic damage. A similar, additive specific locus mutation frequency is obtained with unequal, 1 + 9 Gy X-irradiation when the interval between fractions is 4 days. This is consistent with 500 + 500 R, 4-day and 7-day interval responses obtained previously but again differs from the sub-additive translocation responses obtained with such X-ray fractionation. Taken together with the data from previous studies the present results suggest that (1) 24 h after the first fraction, (a) the surviving stem cell have two components; survivors of the formerly radiosensitive, cycling component of the normal stem cell population and the formerly radioresistant, G0 or arrested G1 cells, which are being 'triggered' into a rapid cell cycle to achieve repopulation of the testis; (b) these two components are of near-equal sensitivity to translocation induction and cell killing, hence the additive translocation yields with equal X-ray fractionations and yields consistent with those extrapolated from lower doses with higher, unequal fractionations, e.g. 1 + 7 Gy, 1 + 9 Gy; but (c) the formerly radioresistant, triggered component is much more sensitive than the surviving cycling component to specific locus mutation and cell killing, hence the augmented mutation response with 500 + 500 R fractionation and the drop in yield with 1 + 9 Gy compared with 100 + 500 R X-irradiation.(ABSTRACT TRUNCATED AT 400 WORDS)
在24小时分次间隔下,对小鼠精原干细胞进行1 + 9 Gy不等量X射线分次照射后获得的特定位点突变频率较低,这与两次照射的累加作用一致。因此,该反应与24小时分次照射500 + 500 R和100 + 500 R时获得的增加的突变频率明显不同。与100 + 500 R反应相比产量较低,这也表明与易位数据存在明显差异,易位数据显示在相同剂量范围内随着第二剂量增加产量会升高。随着第二剂量从500 R增加到9 Gy,特定位点突变产量下降,这表明在第一次照射后存活的干细胞对这类遗传损伤的敏感性存在异质性。当分次间隔为4天时,对小鼠精原干细胞进行1 + 9 Gy不等量X射线照射也可获得类似的累加特定位点突变频率。这与之前获得的500 + 500 R、4天和7天分次间隔的反应一致,但同样与这种X射线分次照射获得的亚累加易位反应不同。结合之前研究的数据,目前的结果表明:(1) 在第一次照射后24小时,(a) 存活的干细胞有两个组成部分;正常干细胞群体中先前对辐射敏感的增殖部分的存活细胞,以及先前对辐射有抗性的G0期或G1期停滞细胞,它们正被“触发”进入快速细胞周期以实现睾丸的再增殖;(b) 这两个组成部分对易位诱导和细胞杀伤的敏感性近乎相等,因此等量X射线分次照射时易位产量呈累加性,且产量与从较低剂量外推到较高不等量分次照射(如1 + 7 Gy、1 + 9 Gy)时的产量一致;但(c) 先前对辐射有抗性的被触发部分对特定位点突变和细胞杀伤比存活的增殖部分更敏感,因此500 + 500 R分次照射时突变反应增强,与100 + 500 R X射线照射相比,1 + 9 Gy时产量下降。(摘要截短于400字)