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Gene expression profiles in human lymphocytes irradiated in vitro with low doses of gamma rays

机译:低剂量γ射线体外照射的人淋巴细胞的基因表达谱

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The molecular mechanisms underlying responses to low radiation doses are still unknown, especially in normal lymphocytes, despite the evidence suggesting specific changes that may characterize cellular responses. Our purpose was to analyze gene expression profiles by DNA microarrays in human lymphocytes after in vitro irradiation (10, 25 and 50 cGy) with gamma rays. A cytogenetic analysis was also carried out for different radiation doses. G(0) lymphocytes were irradiated and induced to proliferate for 48 h; then RNA samples were collected for gene expression analysis. ANOVA was applied to data obtained in four experiments with four healthy donors, followed by SAM analysis and hierarchical clustering. For 10, 25 and 50 cGy, the numbers of significantly (FDR <= 0.05) modulated genes were 86, 130 and 142, respectively, and 25, 35 and 33 genes were exclusively modulated for each dose, respectively. We found CYP4X1, MAPK10 and ATF6 (10 cGy), DUSP16 and RAD51L1 (25 cGy), and RAD50, REV3L and DCLRE1A (50 cGy). A set of 34 significant genes was common for all doses; while SERPINB2 and C14orf104 were up-regulated, CREB3L2, DDX49, STK25 and XAB2 were down-regulated. Chromosome damage was significantly induced for doses >= 10 cGy (total aberrations) and >= 50 cGy (dicentrics/rings). Therefore, low to moderate radiation doses induced qualitative and/or quantitative differences and similarities in transcript profiles, reflecting the type and extent of DNA lesions. The main biological processes associated with modulated genes were metabolism, stress response/DNA repair,cell growth/differentiation, and transcription regulation. The results indicate a potential risk to humans regarding the development of genetic instability and acquired diseases. (c) 2007by Radiation Research Societ.
机译:尽管有证据表明可能是细胞反应特征的特定变化,但对低辐射剂量反应的潜在分子机制仍是未知的,尤其是在正常淋巴细胞中。我们的目的是在体外用γ射线照射(10、25和50 cGy)后,通过DNA芯片分析人类淋巴细胞中的基因表达谱。还针对不同的辐射剂量进行了细胞遗传学分析。 G(0)淋巴细胞被照射并诱导增殖48 h;然后收集RNA样品用于基因表达分析。将方差分析应用于在四个健康捐献者的四个实验中获得的数据,然后进行SAM分析和层次聚类。对于10、25和50 cGy,显着(FDR <= 0.05)调节的基因数分别为86、130和142,并且分别针对每种剂量分别调节了25、35和33个基因。我们发现了CYP4X1,MAPK10和ATF6(10 cGy),DUSP16和RAD51L1(25 cGy),以及RAD50,REV3L和DCLRE1A(50 cGy)。一组34种重要基因在所有剂量下都是相同的。 SERPINB2和C14orf104上调,CREB3L2,DDX49,STK25和XAB2下调。 > = 10 cGy(总像差)和> = 50 cGy(双着丝粒/环)的剂量会明显诱导染色体损伤。因此,低至中等的辐射剂量会导致转录本特征的定性和/或定量差异和相似性,反映出DNA损伤的类型和程度。与调节基因相关的主要生物学过程是代谢,应激反应/ DNA修复,细胞生长/分化和转录调控。结果表明,人类对遗传不稳定和后天疾病的发展具有潜在的风险。 (c)2007年,辐射研究学会。

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