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No Evidence for the in vivo Induction of Genomic Instability by Low Doses of 137Cs Gamma Rays in Bone Marrow Cells of BALB/cJ and C57BL/6J Mice

机译:没有证据表明低剂量的BALB / cJ和C57BL / 6J小鼠骨髓细胞中137Cs伽马射线的体内诱导基因组不稳定性

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In spite of extensive research, assessment of potential health risks associated with exposure to low-dose (≤ 0.1 Gy) radiation is still challenging. We evaluated the in vivo induction of genomic instability, expressed as late-occurring chromosome aberrations, in bone-marrow cells of two strains of mouse with different genetic background, i.e. the radiosensitive BALB/cJ and the radioresistant C57BL/6J strains following a whole-body exposure to varying doses of 137Cs gamma rays (0, 0.05, 0.1, and 1.0 Gy). A total of five mice per dose per strain were sacrificed at various times post-irradiation up to 6 months for sample collections. Three-color fluorescence in situ hybridization for mouse chromosomes 1, 2, and 3 was used for the analysis of stable-aberrations in metaphase-cells. All other visible gross structural-abnormalities involving non-painted-chromosomes were also evaluated on the same metaphase-cells used for scoring the stable-aberrations of painted-chromosomes. Our new data demonstrated in bone-marrow cells from both strains that low doses of low LET-radiation (as low as 0.05 Gy) are incapable of inducing genomic instability but are capable of reducing specific aberration-types below the spontaneous rate with time post-irradiation. However, the results showed the induction of genomic instability by 1.0 Gy of 137Cs gamma rays in the radiosensitive strain only.
机译:尽管进行了广泛的研究,但评估与低剂量(≤0.1 Gy)辐射相关的潜在健康风险仍然具有挑战性。我们评估了两种具有不同遗传背景的小鼠品系(即放射敏感性BALB / cJ和抗放射性C57BL / 6J品系,经过完整的实验后)在骨髓细胞中的基因组不稳定性的体内诱导,表示为后期发生的染色体畸变。暴露于不同剂量的 137 Cs伽玛射线(0、0.05、0.1和1.0 Gy)。在辐照后长达6个月的不同时间处,每株每种剂量共杀死5只小鼠,以收集样品。小鼠染色体1、2和3的三色荧光原位杂交用于分析中期细胞中的稳定畸变。还使用相同的中期细胞对涉及未上漆的染色体的所有其他可见的总体结构异常进行了评估,这些细胞用于评分上漆的染色体的稳定像差。我们的新数据表明,在两种菌株的骨髓细胞中,低剂量的低LET辐射(低至0.05 Gy)均无法诱导基因组不稳定,但能够随时间推移将特定像差类型降低至自发率以下。辐射。然而,结果显示仅1.0 Gy的 137 Cs伽马射线在放射敏感株中引起基因组不稳定性。

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