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首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Distinct area distribution differences of micronuclei induced by clastogenic and aneuploidogenic chemicals in the bone marrow of the CD-1 mouse.
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Distinct area distribution differences of micronuclei induced by clastogenic and aneuploidogenic chemicals in the bone marrow of the CD-1 mouse.

机译:在CD-1小鼠的骨髓中,由分裂性和非整倍性化学物质诱导的微核的不同区域分布差异。

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摘要

To distinguish between aneuploidogenic and clastogenic effects of test chemicals, area distributions of micronuclei (MN) in polychromatic erythrocytes (PE) from the mouse bone marrow were measured using an image analysis system. Triethylenemelamine (TEM), cytosine-beta-D-arabinofuranoside (ara-C), urethane (URT), cyclosphamide (CP), mitomycin C (MMC), colcemid (COL) and tubulazole C (TUB) were investigated for the induction of micronucleus area distributions. The area distribution of micronuclei of untreated mice was also determined. Reproducible small differences between the clastogens and the aneuploidogens were observed after measuring 1100-1200 micronuclei. A common feature of the distribution curves was a shoulder region in the same area range for all clastogens. The aneuploidogens COL and TUB showed a plateau (= wide peak) in this clastogenic shoulder region. For all clastogens, the integrated area of shoulder over a fitted function (shoulder strength) was evaluated. MMC and CP, thought to have some aneuploidogenic potential, showed an increased shoulder strength compared to TEM, ara-C and URT. The control area distribution had no similarities to the area distribution of either clastogens or aneuploidogens. In a further experiment, we attempted to correlate the size of micronuclei determined after treatment with the aneuploidogenic chemicals to the size of whole chromosomes. Micronuclei found by image analysis which bear chromosome-like structures (judged by light microscopy) were manually identified. This selection of micronuclei was area-distributed to determine the mean size of these micronuclei. None of the peaks and plateaus in the area distributions obtained with the aneuploidogenic chemicals could be attributed to the size of a chromosome.
机译:为了区分测试化学物质的非整倍性作用和裂解作用,使用图像分析系统测量了来自小鼠骨髓的多色红细胞(PE)中微核(MN)的面积分布。研究了三亚乙基三聚氰胺(TEM),胞嘧啶-β-D-阿拉伯呋喃糖苷(ara-C),氨基甲酸酯(URT),环磷酰胺(CP),丝裂霉素C(MMC),秋水仙素(COL)和微管唑C(TUB)的诱导作用微核面积分布。还确定了未经处理的小鼠的微核的面积分布。在测量1100-1200个微核后,观察到了克拉斯通和非整倍体之间的可再现小差异。分布曲线的共同特征是所有胶结蛋白在相同面积范围内的肩部区域。非整倍体原COL和TUB在此裂片性肩部区域显示出平稳期(=宽峰)。对于所有胶束原,评估了拟合功能(肩部力量)上的肩部积分面积。与TEM,ara-C和URT相比,被认为具有非整倍性潜力的MMC和CP显示出更高的肩部力量。对照区域的分布与clastogens或非整倍体生成物的区域分布没有相似之处。在另一个实验中,我们试图将用非整倍体化学物质处理后确定的微核大小与整个染色体的大小相关联。通过图像分析发现的带有核样结构(通过光学显微镜判断)的微核被人工鉴定。微核的这种选择是区域分布的,以确定这些微核的平均大小。用非整倍性化学物质获得的峰分布中的峰和平稳都不能归因于染色体的大小。

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