Suppr超能文献

伽马射线照射后人类外周血淋巴细胞的DNA修复能力及静止和增殖状态下DNA修复基因的表达谱

DNA repair capacity after gamma-irradiation and expression profiles of DNA repair genes in resting and proliferating human peripheral blood lymphocytes.

作者信息

Mayer Claudia, Popanda Odilia, Zelezny Otto, von Brevern Marie-Charlotte, Bach Alfred, Bartsch Helmut, Schmezer Peter

机构信息

Division of Toxicology and Cancer Risk Factors, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120, Heidelberg, Germany.

出版信息

DNA Repair (Amst). 2002 Mar 28;1(3):237-50. doi: 10.1016/s1568-7864(01)00019-2.

Abstract

DNA repair plays an important role in maintaining genomic integrity, and deficiencies in repair function are known to promote cancer development. Several studies have used the individual capacity to repair DNA damage in peripheral blood lymphocytes (PBLs) as a cancer risk marker. As the cell's ability to remove DNA damage may be correlated with proliferative activity, it is an important question whether quiescent or dividing cells should be used in such studies. The aim of our study was to compare DNA repair capacity and expression profiles of 70 known DNA repair genes, both in resting and phytohemagglutinin (PHA) stimulated human PBLs. Using the comet assay, gamma-radiation-induced DNA damage and repair in lymphocytes was analyzed. No difference, neither in the rate of radiation-induced DNA damage nor in DNA repair capacity between PHA-stimulated and non-stimulated PBLs was observed. Stimulated cells, however, showed significantly elevated values for background damage. Transcriptional profiles of repair genes were analyzed using cDNA arrays. Hybridization experiments were performed with mRNA isolated from both unstimulated and PHA-stimulated PBLs. More than 70% of all evaluated genes had constant expression levels. Twelve genes responded with a more than two-fold increase of transcripts to the mitogenic stimulus. Most of the up-regulated repair enzymes are also known to play a role in DNA replication. In conclusion, the data presented here suggest that all repair proteins needed for the repair of gamma-irradiation induced DNA-damage, that can be detected by the alkaline comet assay, are already present in G0 cells at sufficient amounts and do not need to be induced once lymphocytes are stimulated to start cycling. Our results thus do not support a general increase in DNA repair activity of PBLs by PHA stimulation, and the use of stimulated PBLs in molecular epidemiological studies on DNA repair of gamma-irradiation induced DNA damage seems not to be mandatory.

摘要

DNA修复在维持基因组完整性方面发挥着重要作用,已知修复功能缺陷会促进癌症发展。多项研究将外周血淋巴细胞(PBL)修复DNA损伤的个体能力用作癌症风险标志物。由于细胞去除DNA损伤的能力可能与增殖活性相关,因此在这类研究中应使用静止细胞还是分裂细胞是一个重要问题。我们研究的目的是比较70个已知DNA修复基因在静息和植物血凝素(PHA)刺激的人PBL中的DNA修复能力和表达谱。使用彗星试验分析了γ射线诱导的淋巴细胞DNA损伤和修复情况。未观察到PHA刺激和未刺激的PBL在辐射诱导的DNA损伤速率或DNA修复能力上有差异。然而,刺激后的细胞背景损伤值显著升高。使用cDNA阵列分析修复基因的转录谱。对从未刺激和PHA刺激的PBL中分离的mRNA进行杂交实验。所有评估基因中超过70%的基因表达水平恒定。12个基因对促有丝分裂刺激的转录本增加了两倍以上。大多数上调的修复酶也已知在DNA复制中起作用。总之,此处呈现的数据表明,通过碱性彗星试验可检测到的γ射线诱导的DNA损伤修复所需的所有修复蛋白,在G0期细胞中已足量存在,淋巴细胞一旦被刺激开始循环就无需诱导。因此,我们的结果不支持PHA刺激会普遍增加PBL的DNA修复活性,在γ射线诱导的DNA损伤的DNA修复分子流行病学研究中使用刺激后的PBL似乎并非必需。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验