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多环芳烃在成年大鼠肝脏上皮细胞完整细胞体系中诱导姐妹染色单体交换

Sister-chromatid exchange induction by polycyclic aromatic hydrocarbons in an intact cell system of adult rat-liver epithelial cells.

作者信息

Tong C, Brat S V, Williams G M

出版信息

Mutat Res. 1981 Nov;91(6):467-73. doi: 10.1016/0165-7992(81)90054-3.

DOI:10.1016/0165-7992(81)90054-3
PMID:7290101
Abstract

Adult rat-liver epithelial cell lines possess intrinsic metabolic capability for the biotransformation of xenobiotics and thus, are sensitive to a broad spectrum of mutagens/carcinogens in a mutagenesis assay at the hypoxanthine-guanine phosphoribosyl transferase locus. To provide another end-point of biological significance in these lines, we have investigated the application of adult rat-liver epithelial cell line 18 in a sister-chromatid exchange assay. Significant dose-dependent increases in the sister-chromatid exchange frequency occurred when liver cells were exposed to benzo[a]pyrene and 7,12-dimethylbenz[a]anthracene. A weak but positive response was elicited by benz[a]anthracene. The present observations thus confirm the capacity of these cells to generate genotoxic metabolites from activation-dependent mutagens/carcinogens and indicate a relationship between the production of mutations and sister-chromatid exchanges by polycyclic aromatic hydrocarbons.

摘要

成年大鼠肝脏上皮细胞系具有对外源化学物质进行生物转化的内在代谢能力,因此,在次黄嘌呤 - 鸟嘌呤磷酸核糖转移酶基因座的诱变试验中,它们对多种诱变剂/致癌物敏感。为了在这些细胞系中提供另一个具有生物学意义的终点指标,我们研究了成年大鼠肝脏上皮细胞系18在姐妹染色单体交换试验中的应用。当肝细胞暴露于苯并[a]芘和7,12 - 二甲基苯并[a]蒽时,姐妹染色单体交换频率出现了显著的剂量依赖性增加。苯并[a]蒽引发了微弱但呈阳性的反应。因此,目前的观察结果证实了这些细胞从依赖激活的诱变剂/致癌物产生遗传毒性代谢物的能力,并表明多环芳烃产生的突变与姐妹染色单体交换之间存在关联。

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引用本文的文献

1
Biomarkers of chromosomal damage in peripheral blood lymphocytes induced by polycyclic aromatic hydrocarbons: a meta-analysis.多环芳烃诱导外周血淋巴细胞染色体损伤的生物标志物:一项荟萃分析。
Int Arch Occup Environ Health. 2012 Jan;85(1):13-25. doi: 10.1007/s00420-011-0629-4. Epub 2011 Apr 2.
2
The lack of genotoxicity of sodium fluoride in a battery of cellular tests.在一系列细胞试验中氟化钠无基因毒性。
Cell Biol Toxicol. 1988 Jun;4(2):173-86. doi: 10.1007/BF00119244.
3
Use of an established human hepatoma cell line with endogenous bioactivation for gene mutation studies.
使用具有内源性生物活化作用的成熟人肝癌细胞系进行基因突变研究。
Cell Biol Toxicol. 1988 Sep;4(3):267-79. doi: 10.1007/BF00058736.