共济失调-毛细血管扩张淋巴母细胞样细胞系的细胞和分子研究。

Kroc Foundation series Pub Date : 1985-01-01
M Fiorilli, M Crescenzi, M Carbonari, G Russo, L Businco, F Aiuti
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引用次数: 0

摘要

我们研究了来自AT患者的淋巴母细胞样细胞系(LCLs)中几种与AT相关的病变。7例at - lcl中有6例对γ辐射的敏感性降低。第七行来自一名t细胞免疫力明显正常的患者,在放射治疗后反应正常。通过SDS-PAGE分析对指数生长at - lcl的组成蛋白进行了评估,结果与正常细胞无显著差异。IgM的合成也很正常,除了一个AT-LCL含有不同大小的天然IgM分子,这与五聚体和低聚体的存在相对应。还原条件下的分析显示正常大小的分泌mu链。最后,我们检查了AT和正常lcl中对应于两个癌基因c-myc和c-myb的mrna,发现一个AT- lcl(即ATL6)中有明显的c-myc过量产生。后一项研究结果表明,由于染色体不稳定和随后的癌基因转位,AT细胞可能容易异常表达细胞癌基因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cellular and molecular studies on ataxia-telangiectasia lymphoblastoid cell lines.

We have examined several AT-related lesions in lymphoblastoid cell lines (LCLs) derived from AT patients. Diminished sensitivity to gamma-irradiation was found in six of seven AT-LCLs. A seventh line, from a patient with apparently normal T-cell immunity, responded normally following radiation. Constitutive proteins from exponentially growing AT-LCLs were assessed by SDS-PAGE analysis and did not differ significantly from normals. IgM synthesis was also normal except for one AT-LCL that contained native IgM molecules of different sizes, corresponding to the presence of pentamers and oligomers. Analysis under reducing conditions showed normal-sized secretory mu-chains. Finally, we examined mRNAs corresponding to two oncogenes, c-myc and c-myb, in AT and normal LCLs and found marked overproduction of c-myc in one AT-LCL (ie,, ATL6). The latter findings suggest that AT cells might be prone to aberrantly express cellular oncogenes as a result of chromosomal instability and consequent transposition of oncogenes.

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