Bláha Pavel, Koshlan Nataliya A, Koshlan Igor V, Petrova Daria V, Bogdanova Yulia V, Govorun Raisa D, Múčka Viliam, Krasavin Evgeny A
Laboratory of Radiation Biology, Joint Institute for Nuclear Research, Joliot--Curie 6, 141980, Dubna, Moscow Region, Russia; Faculty of Nuclear Sciences and Physical Engineering, Czech Technical University in Prague, Břehová 7, 11519, Prague 1, Czech Republic.
Laboratory of Radiation Biology, Joint Institute for Nuclear Research, Joliot--Curie 6, 141980, Dubna, Moscow Region, Russia.
Mutat Res. 2017 Oct;803-805:35-41. doi: 10.1016/j.mrfmmm.2017.08.004. Epub 2017 Aug 31.
Fundamental research on the harmful effects of ionizing radiation on living cells continues to be of great interest. Recently, priority has been given to the study of high-charge and high-energy (HZE) ions that comprise a substantial part of the galactic cosmic ray (GCR) spectra that would be encountered during long-term space flights. Moreover, predictions of the delayed genetic effects of high linear energy transfer (LET) exposure is becoming more important as heavy ion therapy use is increasing. This work focuses mainly on the basic research on the delayed effects of HZE ions on V79 Chinese hamster cells, with emphasis on the induction of HPRT mutations after prolonged expression times (ET). The research was conducted under various irradiation conditions with accelerated ions O (E=35.2MeV/n), Ne (E=47.7MeV/n and 51.8MeV/n), and B (E=32.4MeV/n), with LET in the range from 49 to 149 keV/μm and with Co γ-rays. The HPRT mutant fractions (MF) were detected in irradiated cells in regular intervals during every cell culture recultivation (every 3days) up to approximately 40days (70-80 generations) after irradiation. The MF maximum was reached at different ET depending on ionizing radiation characteristics. The position of the maximum was shifting towards longer ET with increasing LET. We speculate that the delayed mutations are created de novo and that they are the manifestation of genomic instability. Although the exact mechanisms involved in genomic instability initiation are yet to be identified, we hypothesize that differences in induction of delayed mutations by radiations with various LET values are related to variations in energy deposition along the particle track. A dose dependence of mutation yield is discussed as well.
关于电离辐射对活细胞有害影响的基础研究一直备受关注。最近,高电荷和高能(HZE)离子的研究成为重点,这类离子在长期太空飞行中会遇到的银河宇宙射线(GCR)光谱中占很大一部分。此外,随着重离子治疗应用的增加,对高线性能量转移(LET)照射的延迟遗传效应的预测变得越发重要。这项工作主要聚焦于HZE离子对V79中国仓鼠细胞延迟效应的基础研究,重点是延长表达时间(ET)后次黄嘌呤 - 鸟嘌呤磷酸核糖转移酶(HPRT)突变的诱导。研究在多种辐照条件下进行,使用加速离子O(E = 35.2MeV/n)、Ne(E = 47.7MeV/n和51.8MeV/n)和B(E = 32.4MeV/n),LET范围为49至149keV/μm,并使用钴γ射线。在每次细胞培养传代(每3天)的定期时间间隔内,检测辐照细胞中的HPRT突变率(MF),直至辐照后约40天(70 - 80代)。根据电离辐射特性,MF最大值在不同的ET时达到。随着LET增加,最大值的位置向更长的ET移动。我们推测延迟突变是重新产生的,并且它们是基因组不稳定的表现。尽管基因组不稳定起始所涉及的确切机制尚未确定,但我们假设不同LET值的辐射诱导延迟突变的差异与沿粒子轨迹的能量沉积变化有关。还讨论了突变产率的剂量依赖性。