Thierry D, Rigaud O, Duranton I, Moustacchi E, Magdelenat H
Radiat Res. 1985 Jun;102(3):347-58.
Fluorimetric analysis of DNA unwinding, which allows measurement of DNA strand breaks in human leukocytes, has been optimized by reducing the amount of cells required for the test and by modifying the DNA alkali unwinding conditions. This permitted measurement of DNA strand-break induction in cells irradiated with low (0.5-7 Gy) or high doses (5-20 Gy) of gamma rays. Linear dose-response curves were obtained for both dose ranges. Presence of cysteamine during irradiation caused a decrease in the extent of DNA strand breaks. The kinetics of the DNA strand-break rejoining process appeared to be biphasic over the dose range of 2-20 Gy when plotted on a linear vs linear axis (percentage of damage as a function of time). Since the rate of disappearance of damaged DNA was similar for any given dose and for all postirradiation incubation times tested, we have expressed the extent of repair after a given postirradiation incubation as the ratio of the slopes of the regression lines obtained from incubated and nonincubated cells. Leukocytes from 25 healthy donors were analyzed to determine an average value for controls. No difference in the level of DNA strand breaks and the rate of repair of these breaks was observed between leukocytes from three ataxia telangiectasia patients and those from normal donors.
通过减少检测所需的细胞数量并改变DNA碱解旋条件,对用于测量人类白细胞中DNA链断裂的DNA解旋荧光分析进行了优化。这使得能够测量用低剂量(0.5 - 7 Gy)或高剂量(5 - 20 Gy)γ射线照射的细胞中的DNA链断裂诱导情况。在两个剂量范围内均获得了线性剂量反应曲线。照射期间半胱胺的存在导致DNA链断裂程度降低。当在线性与线性轴上绘制(损伤百分比作为时间的函数)时,在2 - 20 Gy的剂量范围内,DNA链断裂重新连接过程的动力学似乎是双相的。由于对于任何给定剂量以及所有测试的照射后孵育时间,受损DNA的消失速率相似,我们将给定照射后孵育后的修复程度表示为从孵育细胞和未孵育细胞获得的回归线斜率之比。分析了25名健康供体的白细胞以确定对照的平均值。在三名共济失调毛细血管扩张症患者的白细胞与正常供体的白细胞之间,未观察到DNA链断裂水平及其修复速率的差异。