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

机译:γ射线辐照后的DNA修复能力以及静止和增殖的人外周血淋巴细胞中DNA修复基因的表达情况。

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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.
机译:DNA修复在维持基因组完整性方面起着重要作用,已知修复功能的不足会促进癌症的发展。数项研究已利用个体修复外周血淋巴细胞(PBLs)中DNA损伤的能力作为癌症危险指标。由于细胞消除DNA损伤的能力可能与增殖活性有关,因此在此类研究中应使用静态还是分裂细胞是一个重要的问题。我们研究的目的是比较70种已知的DNA修复基因在静息和植物血凝素(PHA)刺激下的人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。在PHA刺激的PBL和未刺激的PBL之间,辐射诱导的DNA损伤的速率和DNA修复能力都没有差异。然而,受刺激的细胞显示出背景损伤的明显升高的值。使用cDNA阵列分析修复基因的转录概况。用分离自未刺激的和PHA刺激的PBL的mRNA进行杂交实验。所有评估的基因中有70%以上具有恒定的表达水平。十二个基因对促有丝分裂刺激的转录本增加了两倍以上。还已知大多数上调的修复酶在DNA复制中起作用。总之,这里提供的数据表明,可以通过碱彗星测定法检测到的,由伽马射线辐照引起的DNA修复所需的所有修复蛋白都已经以足够的量存在于G0细胞中,不需要一旦刺激淋巴细胞开始循环诱导。因此,我们的结果不支持通过PHA刺激使PBL的DNA修复活性普遍提高,并且在分子流行病学研究中使用刺激的PBL对γ射线诱导的DNA损伤进行DNA修复似乎不是强制性的。

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