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阿糖胞苷增强共济失调毛细血管扩张症细胞中X射线和紫外线诱导的染色体畸变表达。

Enhanced expression of X-ray- and UV-induced chromosome aberrations by cytosine arabinoside in ataxia telangiectasia cells.

作者信息

Ejima Y, Sasaki M S

出版信息

Mutat Res. 1986 Jan-Feb;159(1-2):117-23. doi: 10.1016/0027-5107(86)90120-x.

Abstract

The effect of cytosine arabinoside (ara-C) on the frequency of X-ray- or UV-induced chromosome aberrations was studied in cultured skin fibroblasts derived from 2 normal persons, 4 ataxia telangiectasia (AT) patients and 2 obligate AT heterozygotes. Density-inhibited cells were irradiated with X-rays or UV, post-treated with ara-C, and chromosomes in the first post-irradiation mitoses were examined. UV, a poor inducer of chromosome-type aberrations in G1, caused chromosome-type aberrations (dicentrics and rings) when coupled with ara-C both in normal and AT cells, but to a much greater extent in AT cells. In AT cells, an elevated induction of both terminal deletions and chromatid aberrations was also observed by the application of UV and ara-C, and unexpectedly, UV alone induced a considerable frequency of both types of aberrations. The enhancing effect of ara-C on X-irradiated cells was less pronounced than on UV-irradiated cells. The responses of AT heterozygotes were virtually the same as those of normal cells. These findings suggest that ara-C can convert the UV-induced DNA damage into the type that has a potential to induce dicentrics and rings in G1 as well as to elicit a hypersensitive response of AT cells.

摘要

研究了阿糖胞苷(ara-C)对2名正常人、4名共济失调毛细血管扩张症(AT)患者和2名AT症携带者的皮肤成纤维细胞培养物中X射线或紫外线诱导的染色体畸变频率的影响。对密度抑制的细胞进行X射线或紫外线照射,用ara-C进行后处理,并检查照射后第一次有丝分裂中的染色体。紫外线在G1期是染色体型畸变的弱诱导剂,在正常细胞和AT细胞中,当与ara-C联合使用时,都会导致染色体型畸变(双着丝粒和环状染色体),但在AT细胞中程度要大得多。在AT细胞中,应用紫外线和ara-C还观察到末端缺失和染色单体畸变的诱导增加,出乎意料的是,单独使用紫外线也会诱导相当频率的这两种类型的畸变。ara-C对X射线照射细胞的增强作用不如对紫外线照射细胞明显。AT症携带者的反应与正常细胞几乎相同。这些发现表明,ara-C可以将紫外线诱导的DNA损伤转化为在G1期有可能诱导双着丝粒和环状染色体的类型,并引发AT细胞的超敏反应。

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