Eguchi-Kasai K, Murakami M, Itsukaichi H, Fukutsu K, Kanai T, Furusawa Y, Sato K, Ohara H, Yatagai F
National Institute of Radiological Sciences, Chiba-shi, Japan.
Adv Space Res. 1996;18(1-2):109-18. doi: 10.1016/0273-1177(95)00797-i.
It can be noted that it is not simple double strand breaks (dsb) but the non-reparable breaks that are associated with high biological effectiveness in the cell killing effect for high LET radiation. Here, we have examined the effectiveness of fast neutrons and low (initial energy = 12 MeV/u) or high (135 MeV/u) energy charged particles on cell death in 19 mammalian cell lines including radiosensitive mutants. Some of the radiosensitive lines were deficient in DNA dsb repair such as LX830, M10, V3, and L5178Y-S cells and showed lower values of relative biological effectiveness (RBE) for fast neutrons if compared with their parent cell lines. The other lines of human ataxia-telangiectasia fibroblasts, irs 1, irs 2, irs 3 and irs1SF cells, which were also radiosensitive but known as proficient in dsb repair, showed moderated RBEs. Dsb repair deficient mutants showed low RBE values for heavy ions. These experimental findings suggest that the DNA repair system does not play a major role against the attack of high linear energy transfer (LET) radiations. Therefore, we hypothesize that a main cause of cell death induced by high LET radiations is due to non-reparable dsb, which are produced at a higher rate compared to low LET radiations.
可以注意到,与高传能线密度(LET)辐射的细胞杀伤效应中高生物学效应相关的并非简单的双链断裂(dsb),而是不可修复的断裂。在此,我们研究了快中子以及低(初始能量 = 12 MeV/u)或高(135 MeV/u)能量带电粒子对19种哺乳动物细胞系(包括辐射敏感突变体)细胞死亡的影响。一些辐射敏感细胞系存在DNA双链断裂修复缺陷,如LX830、M10、V3和L5178Y - S细胞,与它们的亲本细胞系相比,对快中子的相对生物学效应(RBE)值较低。其他人类共济失调 - 毛细血管扩张症成纤维细胞系,irs 1、irs 2、irs 3和irs1SF细胞,虽然也对辐射敏感,但已知双链断裂修复能力正常,其RBE值适中。双链断裂修复缺陷的突变体对重离子的RBE值较低。这些实验结果表明,DNA修复系统在抵抗高传能线密度(LET)辐射的攻击中并不起主要作用。因此,我们推测高LET辐射诱导细胞死亡的主要原因是由于不可修复的双链断裂,与低LET辐射相比,其产生速率更高。