Abramsson-Zetterberg L, Zetterberg G, Grawé J
Department of Genetics, Uppsala University, Sweden.
Mutat Res. 1996 Mar 9;350(2):349-58. doi: 10.1016/0027-5107(95)00208-1.
The time-course of micronucleated polychromatic erythrocytes (MPCE) in mouse bone marrow and peripheral blood, induced by an acute 0.1 Gy dose of X-rays, was determined using flow cytometric analysis, which made frequent sampling possible and allowed use of a dose low enough not to affect erythroid cell proliferation. The frequency of MPCE (fMPCE) began to increase in the bone marrow at 10 h after irradiation and reached a maximum at 28 h after irradiation. In the peripheral blood fMPCE began to increase at 20 h after irradiation and peaked at about 40 h after irradiation. The time-course found is discussed on the basis of data on the differentiation of erythroid cells. The results indicate that the micronuclei registered in polychromatic erythrocytes may originate from lesions induced not only during the last cell cycle but also during earlier ones. After an acute dose of 1.0 Gy of X-rays the maximum fMPCE was delayed both in bone marrow and peripheral blood reflecting an effect on the cell cycle progression of erythroblasts.
采用流式细胞术分析测定了急性0.1 Gy X射线剂量诱导的小鼠骨髓和外周血中微核多染性红细胞(MPCE)的时间进程,该方法使得频繁取样成为可能,并允许使用足够低的剂量以免影响红系细胞增殖。MPCE频率(fMPCE)在照射后10小时开始在骨髓中增加,并在照射后28小时达到最大值。在外周血中,fMPCE在照射后20小时开始增加,并在照射后约40小时达到峰值。根据红系细胞分化的数据对所发现的时间进程进行了讨论。结果表明,多染性红细胞中记录的微核可能不仅源于最后一个细胞周期,还源于更早的细胞周期所诱导的损伤。急性1.0 Gy X射线剂量照射后,骨髓和外周血中fMPCE的最大值均延迟出现,这反映了对成红细胞细胞周期进程的影响。