Schmid E, Braselmann H, Nahrstedt U
Institut für Strahlenbiologie, GSF-Forschungszentrum, Oberschleissheim, Germany.
Mutat Res. 1995 Nov;348(3):125-30. doi: 10.1016/0165-7992(95)00056-9.
In an earlier work stable aberrations and dicentrics were determined by fluorescence in situ hybridization (FISH) after various doses of 137Cs gamma-rays. No corresponding calibration curve for dicentrics is available for determinations in terms of the conventional analysis as performed in our laboratory. In view of the potential for the application of chromosome painting to human biological dosimetry, it is desirable to determine such a calibration curve and this and the comparison of the resulting data to those obtained in terms of the FISH method is the objective of the present communication. In the study it is found that the linear-quadratic dose response curves for dicentrics, that are determined by the two methods, are significantly different, although the different target sizes are accounted for. A similar problem was found earlier for X-rays. It does not appear that the difference is due to technical difficulties in the FISH method, that has been improved by employing in addition to the whole chromosome DNA probes, a pan-centromeric DNA probe.
在早期的一项工作中,通过荧光原位杂交(FISH)测定了不同剂量的137Csγ射线照射后的稳定畸变和双着丝粒。在我们实验室进行的常规分析中,没有相应的双着丝粒校准曲线可用于测定。鉴于染色体涂染在人类生物剂量测定中的应用潜力,确定这样一条校准曲线是很有必要的,而本文的目的就是确定这条校准曲线,并将所得数据与通过FISH方法获得的数据进行比较。在该研究中发现,尽管考虑了不同的靶尺寸,但通过两种方法测定的双着丝粒的线性二次剂量反应曲线存在显著差异。早些时候在X射线研究中也发现了类似的问题。这种差异似乎并非由于FISH方法存在技术困难,因为除了全染色体DNA探针外,还使用了泛着丝粒DNA探针,FISH方法已经得到了改进。