Cytotoxic effect and induction of sister chromatid exchange in exponentially growing rat 9L gliosarcoma cells after brief exposure to BrdU.

R X Zhang, T Nagashima, T Hoshino
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引用次数: 15

Abstract

The magnitude of DNA modulation in rat 9L gliosarcoma cells after a brief exposure to bromodeoxyuridine (BrdU) was studied by assaying colony-forming efficiency (CFE) and the number of sister chromatid exchanges (SCEs) per metaphase. The CFE assay showed that a 1-hr exposure to BrdU, at concentrations ranging from 10 to 1000 microM, produced a maximum cell kill of 5%. After a 2-hr exposure to 20 microM BrdU, the surviving fraction was 0.99, and even at a BrdU concentration of 1000 microM, 77% of the 9L cells survived. Compared with control cultures, the relative number of SCEs per metaphase in treated cultures was increased after a 1-hr exposure to BrdU at concentrations of 100 microM or more and after a 2-hr exposure to concentrations of 20 microM or more; no increase was observed in cells treated for 30 min with BrdU at concentrations up to 1000 microM. When the treated cells were allowed to grow in BrdU-free growth medium, the number of SCEs per metaphase returned to the control level within 24 hr, even after exposure to BrdU at concentrations as high as 1000 microM. These results demonstrate that exposure to BrdU at concentrations of up to 1000 microM for 30 min, 100 microM for 1 hr, and 20 microM for 2 hr causes little modulation of DNA.

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短暂暴露于BrdU后指数生长大鼠9L胶质瘤细胞的细胞毒作用和诱导姐妹染色单体交换。
研究了大鼠9L胶质瘤细胞短暂暴露于溴脱氧尿苷(BrdU)后DNA的调节程度,方法是测定细胞的集落形成效率(CFE)和每个中期姐妹染色单体交换(SCEs)的数量。CFE试验表明,在10至1000微米的浓度范围内,暴露于BrdU 1小时可产生5%的最大细胞杀伤。BrdU浓度为1000 μ m时,9L细胞存活率为77%,BrdU浓度为20 μ m时,9L细胞存活率为0.99。与对照培养物相比,在100微米或更高浓度的BrdU暴露1小时和20微米或更高浓度的BrdU暴露2小时后,处理培养物中每个中期sce的相对数量增加;BrdU浓度高达1000微米,处理30分钟后,细胞未见增加。当处理后的细胞在不含BrdU的培养基中生长时,即使暴露于浓度高达1000微米的BrdU中,每个中期的sce数量在24小时内也恢复到对照水平。这些结果表明,暴露于浓度高达1000微米的BrdU中30分钟,100微米的1小时和20微米的2小时对DNA的调节作用很小。
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Abstracts of the joint meeting of the Cell Kinetics Society and the International Cell Cycle Society. 28-31 March 1990, St Louis, Missouri, U.S.A. Abstracts of the 16th meeting of the European Study Group for Cell Proliferation. 3-6 May 1989, Milan. Proceedings of the Cell Kinetics Society, thirteenth annual meeting. 29 March-1 April 1989, White Plains, New York, U.S.A. Bone marrow fibroblast colony-forming cells are osteogenic stem cells. Epidermal tissue homeostasis. III. Effect of hydrocortisone on cell pool size, cell birth rate and cell loss in normal toads and in toads deprived of the pars distalis of the pituitary gland.
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