γ辐照诱导的可变放射敏感性慢性淋巴细胞白血病细胞DNA单双链断裂及其修复。

M H Myllyperkiö, T R Koski, L M Vilpo, J A Vilpo
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引用次数: 26

摘要

用碱性和中性彗星法研究了γ辐照诱导的正常造血细胞和白血病淋巴细胞DNA单链和双链断裂(SSB和DSB)形成及其修复动力学。采用密度梯度离心法从慢性淋巴细胞白血病(CLL)患者和健康受试者的外周血中分离出细胞。此外,用免疫磁珠从非白血病人骨髓中分离CD34+祖细胞进行了研究。采用放射性亮氨酸结合法测定137Cs辐照对36例慢性淋巴细胞白血病患者和8例健康供者外周血单核淋巴细胞的体外细胞毒性。当细胞暴露于高达10.4 Gy的γ辐照剂量时,在碱性(SSBs)和中性(DSBs)凝胶电泳中观察到DNA迁移的剂量依赖性增加。2.4和5.4 Gy辐照后,细胞几乎完全修复了单链和双链断裂。DNA链断裂的形成和修复在所有被调查的正常细胞群和CLL细胞中基本上是相似的。γ辐射诱导的细胞毒性与DNA链断裂形成和修复能力无关。根据这些结果,个体CLL病例和健康人之间γ辐照耐受性的差异可以解释为DNA链断裂形成或修复之外的其他方面。
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Gamma-irradiation-induced DNA single- and double-strand breaks and their repair in chronic lymphocytic leukemia cells of variable radiosensitivity.

Gamma-irradiation-induced DNA single- and double-strand break (SSB and DSB) formation and their repair kinetics in normal hematopoietic cells and in leukemic lymphocytes was investigated using alkaline and neutral comet assays. The cells were isolated by density gradient centrifugation from peripheral blood of patients with chronic lymphocytic leukemia (CLL) and from healthy study subjects. Furthermore, CD34+ progenitor cells isolated with immunomagnetic beads from bone marrow of non-leukemic persons were investigated. The cytotoxicity of 137Cs irradiation was determined in vitro in peripheral blood mononuclear lymphocytes from 36 CLL patients and from 8 healthy donors using radioactive leucine incorporation assay in 4-day culture. A dose-dependent increase in DNA migration was observed in alkaline (SSBs) and neutral (DSBs) gel electrophoresis when the cells were exposed to gamma-irradiation doses up to 10.4 Gy. After irradiation with doses of 2.4 and 5.4 Gy, the cells repaired their single- and double-strand breaks almost completely. The formation and repair of DNA strand breaks were essentially similar in all normal cell populations investigated and in CLL cells. The gamma-irradiation-induced cytotoxicity did not correlate with DNA strand break formation and repair capacity. According to these results, the differences of gamma-irradiation tolerance among individual CLL cases and among healthy persons are explicable in terms other than DNA strand break formation or repair.

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