Foresti M, Migliore L
Dipt. Genetica, Biologia generale e molecolare, Università Federico II, Napoli, Italy.
Cell Biol Toxicol. 1993 Oct-Dec;9(4):377-84. doi: 10.1007/BF00754466.
Bacitracin, an antibiotic widely utilized in clinical and veterinary use, was tested on murine erythroleukemia (MEL) cells. Tests were performed to evaluate the capacity of the drug to interfere with erythroid differentiation. Cells were exposed to a single treatment in S phase at sublethal doses of bacitracin. Two responses were found depending on the drug concentration. At higher concentrations (25 micrograms/ml and 250 ng/ml) a reduction in number of differentiating cells was observed but the kinetics of the process remained unchanged. At lower concentrations (from 2.5 ng/ml to 2.5 fg/ml) a dramatic alteration of the dynamic of differentiation was found. These two responses are related to different activities of the DNA repair mechanisms. Higher doses of bacitracin stimulate repair while lower concentrations are not able to active repair, as demonstrated by tests with hydroxyurea. The bacitracin-induced damage can be considered a stable genetic and/or epigenetic alteration, as demonstrated by the high frequency of mutant clones isolated from low-dose treated cells. The suitability of MEL cells system in evaluating genotoxicity of drugs for veterinary use is underlined.
杆菌肽是一种广泛应用于临床和兽医领域的抗生素,已在小鼠红白血病(MEL)细胞上进行了测试。进行这些测试是为了评估该药物干扰红细胞分化的能力。细胞在S期以亚致死剂量的杆菌肽进行单次处理。根据药物浓度发现了两种反应。在较高浓度(25微克/毫升和250纳克/毫升)下,观察到分化细胞数量减少,但该过程的动力学保持不变。在较低浓度(从2.5纳克/毫升到2.5飞克/毫升)下,发现分化动态发生了显著改变。这两种反应与DNA修复机制的不同活性有关。如用羟基脲进行的测试所示,较高剂量的杆菌肽刺激修复,而较低浓度则无法激活修复。杆菌肽诱导的损伤可被视为一种稳定的遗传和/或表观遗传改变,从低剂量处理细胞中分离出的突变克隆的高频率就证明了这一点。强调了MEL细胞系统在评估兽用药物遗传毒性方面的适用性。