Tallon I, Verschaeve L, Kirsch-Volders M
Laboratory for Anthropogenetics, Free University Brussels, Belgium.
Microsc Res Tech. 1998 Mar 1;40(5):344-53. doi: 10.1002/(SICI)1097-0029(19980301)40:5<344::AID-JEMT2>3.0.CO;2-R.
Although ionising radiation mainly induces DNA strand breaks leading to chromosomal aberrations, there are indications that it also might induce numerical chromosome aberrations (aneuploidy). The existing data, however, do not provide evidence for a mechanism. To assess the relative sensitivity of the G1 vs. G2 cellular targets, whole blood cultures of lymphocytes were irradiated in vitro with different doses of X-rays (0.5, 1 and 2 Gy). The lymphocytes were harvested after cytochalasin-B blockade to allow the selective study of binucleated cells, having undergone only one division in culture. Harvesting was performed at different sampling times (70, 74, and 78 hours). To evaluate the micronuclei, regarding whole chromosomes or acentric fragments, an oligonucleotide probe that recognises the centromeric region of all human chromosomes was used. The relative percentage of centromere-positive micronuclei ranged from 5 up to 18% depending on the cell cycle stage and on the received dose. Cells exposed during the G1 phase exhibited a slightly higher frequency of centromere-positive micronuclei than cells that were in G2 at the time of exposure. G1 exposure induced a centromere-positive micronuclei dose-effect relationship that was not observed after G2 exposure. The observed difference in response of both phases on the centromere-positive micronuclei yields may be due to the involvement of different targets.
尽管电离辐射主要诱导DNA链断裂从而导致染色体畸变,但有迹象表明它也可能诱导染色体数目畸变(非整倍体)。然而,现有数据并未提供相关机制的证据。为了评估G1期与G2期细胞靶点的相对敏感性,用不同剂量的X射线(0.5、1和2 Gy)对淋巴细胞的全血培养物进行体外照射。在用细胞松弛素B阻断后收获淋巴细胞,以便对仅在培养中经历一次分裂的双核细胞进行选择性研究。在不同的采样时间(70、74和78小时)进行收获。为了评估关于整条染色体或无着丝粒片段的微核,使用了一种识别所有人类染色体着丝粒区域的寡核苷酸探针。着丝粒阳性微核的相对百分比根据细胞周期阶段和所接受的剂量在5%至18%之间。在G1期暴露的细胞比在暴露时处于G2期的细胞表现出略高的着丝粒阳性微核频率。G1期暴露诱导了着丝粒阳性微核的剂量效应关系,而G2期暴露后未观察到这种关系。两个阶段对着丝粒阳性微核产量的反应差异可能是由于不同靶点的参与。