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溴脱氧尿苷在体外标记植入前小鼠胚胎姐妹染色单体分化过程中的细胞毒性和遗传毒性作用。

Cytotoxic and genotoxic effects of bromodeoxyuridine during in vitro labelling for sister-chromatid differentiation in preimplantation mouse embryos.

作者信息

Vogel R, Spielmann H

机构信息

Max von Pettenkofer Institute, Federal Health Office (BGA), Berlin (West), (F.R.G.).

出版信息

Mutat Res. 1988 Sep-Oct;209(1-2):75-8. doi: 10.1016/0165-7992(88)90114-5.

Abstract

Exposure of preimplantation mouse embryos in culture to bromodeoxyuridine (BrdU) in the concentration range of 10(-9) to 2 x 10(-6) M allows sister-chromatid differentiation at the morula and blastocyst stage. The same BrdU concentrations induced no chromosomal aberrations, but a prolongation of the cell cycle and an increase of the SCE frequency. Even at the lowest BrdU concentration for sister-chromatid differentiation (10(-9) M the background level for SCE was found to be significantly higher in early embryos than in fetal or adult tissues of the mouse. Therefore, the high SCE frequency seems to be characteristic of undifferentiated embryonic cells. Methodological recommendations are also given for SCE assay in preimplantation mouse embryos.

摘要

将着床前小鼠胚胎在培养中暴露于浓度范围为10⁻⁹至2×10⁻⁶M的溴脱氧尿苷(BrdU)下,可使桑椹胚和囊胚阶段的姐妹染色单体发生分化。相同的BrdU浓度未诱导染色体畸变,但会延长细胞周期并增加姐妹染色单体交换(SCE)频率。即使在用于姐妹染色单体分化的最低BrdU浓度(10⁻⁹M)下,也发现早期胚胎中SCE的背景水平显著高于小鼠的胎儿或成年组织。因此,高SCE频率似乎是未分化胚胎细胞的特征。还给出了着床前小鼠胚胎中SCE检测的方法学建议。

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