A comet assay study reveals that aluminium induces DNA damage and inhibits the repair of radiation-induced lesions in human peripheral blood lymphocytes

被引:113
作者
Lankoff, A
Banasik, AB
Duma, A
Ochniak, E
Lisowska, H
Kuszewski, T
Gózdz, S
Wojcik, A
机构
[1] Jan Kochanowski Univ Humanities & Sci, Inst Biol, Dept Radiobiol & Immunol, PL-25406 Kielce, Poland
[2] Swietokrzyskie Oncol Ctr, Kielce, Poland
[3] Inst Nucl Chem & Technol, Dept Radiobiol & Hlth Protect, PL-03195 Warsaw, Poland
关键词
aluminium; comet assay; DNA single strand breaks; oxidative DNA damage; DNA repair; human lymphocytes; ionizing radiation;
D O I
10.1016/j.toxlet.2005.07.012
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Although it is known that many metals induce DNA damage and inhibit DNA repair, information regarding aluminium (Al) is scarce. The aim of this study was to analyze the level of DNA damage in human peripheral blood lymphocytes treated with At and the impact of Al on the repair of DNA damage induced by ionizing radiation. Cells were treated with different doses of aluminium chloride (1, 2, 5, 10 and 25 mu g/ml AlCl3) for 72 h. The level of DNA damage and of apoptosis was determined by the comet assay. The level of oxidative damage was determined by the application of endonuclease III and formamidopyrimidine DNA glycosylase. The results on apoptosis were confirmed by flow cytometry. Based on the fluorescence intensity, cells were divided into cohorts of different relative DNA content that corresponds to G(1), S and G(2) phases of the cell cycle. Our results revealed that At induces DNA damage in a dose-dependent manner, however, at the dose of 25 mu g/ml the level of damage declined. This decline was accompanied by a high level of apoptosis indicating selective elimination of damaged cells. Cells pre-treated with At showed a decreased repair capacity indicating that Al inhibits DNA repair. The possible mechanisms by which Al induces DNA damage and inhibits the repair are discussed. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:27 / 36
页数:10
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