首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >An investigation of the cytotoxic and mutagenic potential of low intensity laser irradiation in Friend erythroleukaemia cells.
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An investigation of the cytotoxic and mutagenic potential of low intensity laser irradiation in Friend erythroleukaemia cells.

机译:低强度激光照射对Friend红白血病细胞的细胞毒性和诱变潜力的研究。

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摘要

The purpose of this study was to investigate the cytotoxic and genotoxic potential of low intensity laser irradiation (660 nm, 12 mW, 5 kHz) on mammalian cells. Thymidine kinase (TK)-positive and TK-deficient Friend erythroleukaemia (FEL) cells, clone 707 and subclone 707BUF respectively, were used in this investigation. Following irradiation of exponentially growing cells in suspension at doses of 2 and 20 J/cm2 a number of sensitive bioassays were used to facilitate the detection of laser-induced mutations, DNA damage and cell killing. Mutations were assessed by the examination of chromosome spreads, the determination of micronucleus frequency and by the determination of the mutant frequency at the hypoxanthine-guanine phosphoribosyltransferase (hgprt) locus. DNA damage was quantified using a sensitive ELISA. The cytotoxic effect of laser irradiation was assessed using a cloning assay. The results of this investigation did not show any significant increase in mutation frequency, DNA damage or cell survival in the laser-irradiated cells, compared to sham-irradiated controls. The lack of any demonstrable cytotoxic and genotoxic effects of low intensity laser irradiation on mammalian cells in culture would support it as being a safe modality for clinical use.
机译:这项研究的目的是研究低强度激光照射(660 nm,12 mW,5 kHz)对哺乳动物细胞的细胞毒性和遗传毒性。胸苷激酶(TK)阳性和TK缺陷Friend红细胞白血病(FEL)细胞,分别是克隆707和亚克隆707BUF,用于这项研究。在以2和20 J / cm2的剂量照射悬浮液中呈指数增长的细胞后,使用了许多灵敏的生物测定方法来促进激光诱导的突变,DNA损伤和细胞杀伤的检测。通过检查染色体分布,确定微核频率以及通过确定次黄嘌呤-鸟嘌呤磷酸核糖基转移酶(hgprt)基因座的突变频率来评估突变。使用敏感的ELISA定量DNA损伤。使用克隆测定法评估激光照射的细胞毒性作用。这项研究的结果表明,与假照射的对照组相比,激光照射的细胞的突变频率,DNA损伤或细胞存活率均未显着增加。低强度激光照射对培养的哺乳动物细胞缺乏任何可证明的细胞毒性和遗传毒性作用,将支持它作为临床使用的安全方式。

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