Abstract

The radiobiological effects of accelerated ions with high charge and high energy (HZE) on mammalian cells and their propagation in time are still not sufficiently explained and attract great deal of attention. This work aims to compare the immediate and delayed effects with emphasis on the latter. As shown by our group, the dependence of mutant fraction on expression time after irradiation may have interesting, non-monotonic, character depending on LET (linear energy transfer) of the used heavy ions. We speculate that this phenomenon may occur due to the induced genomic instability. Another area of our research is the study of the DNA structural changes in these mutants induced at different expression times. Chinese hamster V79 cells were irradiated with accelerated ions 11B, 18O, 20Ne, and gamma radiation. The LET was ranging from 0.23 keV/μm of 60Co gamma rays up to 136 keV/μm of 20Ne ions. DNA of unique HPRT mutants was isolated, concentration measured, HPRT exons amplified, and analyzed at several different time points, up to about 40 days, after exposure. Over 1200 HPRT mutants were analyzed for deletions of exons and sorted into three main categories: partial deletion, PD—with deletion of one to eight exons; total deletions, TD—with all nine exons deleted; and no deletions—no change in the HPRT structure observed. In general, the number of samples with partial deletion was increasing with LET of the used radiation, suggesting that higher energy deposition to the cell nucleus is more likely to cause larger structural changes. In the case of total deletions, increase in their number with LET was observed up to LET ∼115 keV/μm followed by a sharp decrease. The samples were also analyzed for the distribution of deletions, in particular exons at various expression times, the so-called mutational patterns. Hypothesis of the mechanisms behind observed phenomena is given, and possible implications for further research are discussed.

Highlights

  • Accelerated heavy ions (HZE: high Z, high energy) are in the focus of biophysical and radiobiological research fields for some time

  • The hypoxanthine–guanine phosphoribosyltransferase (HPRT) gene mutation assay is a well-known system for easy mutagenic studies, based on the 6thioguanine (6-TG) mutant selection [10], which has been widely used to study the mutagenic effects of ionizing radiation (IR) of various qualities in mammalian cell cultures [11,12,13,14,15,16]

  • It was shown that the fraction of exon partial deletions in HPRT gene was increasing with LET of the used radiation in the tested range from 0.23 keV/μm of gamma radiation to 136 keV/μm of 20Ne ions

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Summary

Introduction

Accelerated heavy ions (HZE: high Z, high energy) are in the focus of biophysical and radiobiological research fields for some time now. The knowledge of biological effects of HZE ions is limited compared to sparsely. Ion induced HPRT structural changes ionizing radiation such as gamma rays or X-rays, due to the limited availability of ion-capable accelerators usable for irradiation of biological samples. Research focusing on the mutation induction, their type, and the radiation-induced genomic instability is significant for understanding of the long-term effects of radiation, probably more than the cell killing [4]. The hypoxanthine–guanine phosphoribosyltransferase (HPRT) gene mutation assay is a well-known system for easy mutagenic studies, based on the 6thioguanine (6-TG) mutant selection [10], which has been widely used to study the mutagenic effects of ionizing radiation (IR) of various qualities in mammalian cell cultures [11,12,13,14,15,16]

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