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首页> 外文期刊>Mutation Research - Genetic Toxicology and Environmental Mutagenesis >Sub-micrometer 20 MeV protons or 45 MeV lithium spot irradiation enhances yields of dicentric chromosomes due to clustering of DNA double-strand breaks
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Sub-micrometer 20 MeV protons or 45 MeV lithium spot irradiation enhances yields of dicentric chromosomes due to clustering of DNA double-strand breaks

机译:亚微米20 MeV质子或45 MeV锂点辐射由于DNA双链断裂的聚集而提高了双中心染色体的产量

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In conventional experiments on biological effects of radiation types of diverse quality, micrometerscale double-strand break (DSB) clustering is inherently interlinked with clustering of energy deposition events on nanometer scale relevant for DSB induction. Due to this limitation, the role of the micrometer and nanometer scales in diverse biological endpoints cannot be fully separated. To address this issue, hybrid human-hamster A(L) cells have been irradiated with 45 MeV (60 keV/mu m) lithium ions or 20 MeV (2.6 keV/mu m) protons quasi-homogeneously distributed or focused to 0.5 x 1 mu m(2) spots on regular matrix patterns (point distances up to 10.6 x 10.6 mu m), with pre-defined particle numbers per spot to provide the same mean dose of 1.7 Gy. The yields of dicentrics and their distribution among cells have been scored. In parallel, track-structure based simulations of DSB induction and chromosome aberration formation with PARTRAC have been performed. The results show that the sub-micrometer beam focusing does not enhance DSB yields, but significantly affects the DSB distribution within the nucleus and increases the chance to form DSB pairs in close proximity, which may lead to increased yields of chromosome aberrations. Indeed, the experiments show that focusing 20 lithium ions or 451 protons per spot on a 10.6 mu m grid induces two or three times more dicentrics, respectively, than a quasi-homogenous irradiation. The simulations reproduce the data in part, but in part suggest more complex behavior such as saturation or overkill not seen in the experiments. The direct experimental demonstration that sub-micrometer clustering of DSB plays a critical role in the induction of dicentrics improves the knowledge-on the mechanisms by which these lethal lesions arise, and indicates how the assumptions of the biophysical model could be improved. It also provides a better understanding of the increased biological effectiveness of high-LET radiation. (C) 2015 Elsevier B.V. All rights reserved.
机译:在有关质量不同的辐射类型的生物学效应的常规实验中,微米级双链断裂(DSB)聚类与与DSB诱导有关的纳米级能量沉积事件聚类固有地相互联系。由于此限制,微米和纳米标度在各种生物学终点中的作用无法完全分开。为了解决此问题,已使用45 MeV(60 keV /μm)锂离子或20 MeV(2.6 keV /μm)质子准均质分布或聚焦到0.5 x 1的混合型人仓鼠A(L)细胞进行辐照。常规矩阵图案上的μm(2)点(点距最大为10.6 x 10.6μm),每个点具有预定义的颗粒数,以提供1.7 Gy的相同平均剂量。已对双着丝粒的产量及其在细胞之间的分布进行了评分。并行地,已经进行了基于轨道结构的利用PARTRAC的DSB诱导和染色体畸变形成的模拟。结果表明,亚微米光束聚焦不会提高DSB的产量,但会显着影响DSB在原子核内的分布,并增加形成DSB对紧密结合的机会,这可能导致染色体畸变的产量增加。确实,实验表明,将每个点20个锂离子或451质子聚焦在10.6微米网格上会比准均质辐照分别引起两倍或三倍的双心率。模拟部分重现了数据,但部分暗示了更复杂的行为,例如在实验中未发现的饱和或过度杀伤。直接实验证明,DSB的亚微米簇在诱导双着丝粒中起着关键作用,从而提高了对这些致死性损伤发生机理的认识,并指出了如何改善生物物理模型的假设。它还可以更好地了解高LET辐射的增强的生物有效性。 (C)2015 Elsevier B.V.保留所有权利。

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