Balogh Attila, Paragh György, Juhász Attila, Köbling Tamás, Törocsik Dániel, Mikó Edit, Varga Viktória, Emri Gabriella, Horkay Irén, Scholtz Beáta, Remenyik Eva
Department of Dermatology, Medical and Health Science Center, University of Debrecen, Debrecen, Hungary Nagyerdei Körut 98, H-4032 Debrecen, Hungary.
J Photochem Photobiol B. 2008 Dec 11;93(3):133-9. doi: 10.1016/j.jphotobiol.2008.07.010. Epub 2008 Aug 14.
Real time quantitative reverse transcription-polymerase chain reaction (qRT-PCR) is a sensitive and highly reproducible method often used for determining mRNA levels. To enable proper comparison of gene expression genes expressed at stabile levels within the cells in the studied experimental system need to be identified and used as reference. Ultraviolet B (UVB) radiation is an exogenous carcinogenic stimulus in keratinocytes, and UVB elicited changes have extensively been studied by qRT-PCR, yet a comparison of commonly used reference genes in UVB treatment is lacking. To find the best genes for compensating slight inter-sample variations in keratinocytes in UVB experiments and to understand the potential effects of improper reference gene (RG) selection we have analyzed the mRNA expression of 10 housekeeping genes in neonatal human epidermal keratinocytes (NHEK) after UVB treatment. The biological effect of the used UVB light source was validated by trypane blue exclusion, MTT and comet assays. 20-40mJ/cm(2) dose was chosen for the experiments. The stability of the 10 RGs was assessed by the GeNorm and Normfinder software tools. Regardless of their slightly different algorithm the programs found succinate dehydrogenase complex subunit A (SDHA) to be the best individual RG and SDHA and phosphoglycerate kinase-1 (PGK1) as the most suitable combination. Analysis of the expression of tumor necrosis factor alpha (TNFalpha) and vascular endothelial growth factor (VEGF) found that while the perception of changes in TNF-alpha, a gene undergoing marked upregulation after UVB irradiation is independent of the used RG, changes seen in the more modestly upregulated VEGF are greatly effected by reference gene selection. These findings highlight the importance of reference gene selection in UVB irradiation experiments, and provide evidence that using SDHA or the combination of SDHA and PGK1 as standards could be a reliable method for normalizing qRT-PCR results in keratinocytes after UVB treatment.
实时定量逆转录-聚合酶链反应(qRT-PCR)是一种灵敏且高度可重复的方法,常用于测定mRNA水平。为了能够在研究的实验系统中对细胞内稳定表达水平的基因表达进行恰当比较,需要鉴定并使用稳定表达的基因作为参照。紫外线B(UVB)辐射是角质形成细胞中的一种外源性致癌刺激因素,通过qRT-PCR对UVB引发的变化进行了广泛研究,但缺乏对UVB处理中常用参照基因的比较。为了找到补偿UVB实验中角质形成细胞样本间微小差异的最佳基因,并了解不当选择参照基因(RG)的潜在影响,我们分析了UVB处理后新生儿人表皮角质形成细胞(NHEK)中10个管家基因的mRNA表达。通过台盼蓝排斥试验、MTT和彗星试验验证了所用UVB光源的生物学效应。实验选择了20 - 40mJ/cm²的剂量。通过GeNorm和Normfinder软件工具评估了10个RG的稳定性。尽管它们的算法略有不同,但程序发现琥珀酸脱氢酶复合体亚基A(SDHA)是最佳的单个RG,而SDHA和磷酸甘油酸激酶-1(PGK1)是最合适的组合。对肿瘤坏死因子α(TNFα)和血管内皮生长因子(VEGF)表达的分析发现,虽然UVB照射后显著上调的基因TNF-α的变化感知与所用RG无关,但上调程度较小的VEGF的变化受参照基因选择的影响很大。这些发现突出了UVB照射实验中参照基因选择的重要性,并提供了证据表明使用SDHA或SDHA与PGK1的组合作为标准可能是使UVB处理后角质形成细胞的qRT-PCR结果标准化的可靠方法。