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Analysis of mRNA expression profiles highlights alterations in modulation of the DNA damage-related genes under butanal exposure in A549 human alveolar epithelial cells

机译:mRNA表达谱分析突出显示了在A549人肺泡上皮细胞中,在肛管暴露下DNA损伤相关基因的调控改变

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摘要

Butanal is a lower-molecular-weight saturated aliphatic aldehyde (LSAA) that is known as one of the important causes of indoor pollution. Although a few studies have been reported, the toxicity of butanal and its underlying mechanisms remain unclear. This study focused on toxicity of butanal with microarray analysis relationships of gene expression patterns between vehicle control and two different concentrations of butanal-treated groups. For a comprehensive examination of butanal effects on gene expression, we exposed human alveolar epithelial (A549) cells to IC5 and IC20 for 48 h and compared the gene expression of treated cells with that of vehicle controls using a human oligonucleotide chip. We identified genes that were changed by more than 1.5-fold through gene expression profile analysis. Transcriptomic profiling indicated different gene expression patterns in vehicle control and butanal-exposed groups and showed that the butanal-exposure group had a higher sensitivity to gene alteration than the control group. Through gene expression profile cluster analysis, we identified 2,998 (1,379 up- and 1,619 down-regulated) in the butanal IC5 groups and 3,200 genes (1,369 up- and 1,831 downregulated) in the butanal IC20 groups, with 2,710 (1,281 up- and 1,429 down-regulated) specific genes in common. Through Gene Ontology (GO) analysis with these commonly expressed genes reported the several key biological processes which are known as related to DNA damage responses such as “regulation of apoptosis”, “regulation of cell proliferation”, “immune response”, “inflammatory response”. We confirmed the functional changes using a cellular assay.
机译:丁醛是一种低分子量的饱和脂肪族醛(LSAA),被认为是造成室内污染的重要原因之一。尽管已经报道了一些研究,但是丁醛的毒性及其潜在机制仍不清楚。这项研究集中于丁醛的毒性,并通过微阵列分析载体对照与两种不同浓度的丁醛治疗组之间的基因表达模式之间的关系。为了全面检查丁醛对基因表达的影响,我们将人肺泡上皮(A549)细胞暴露于IC5和IC20 48小时,并使用人寡核苷酸芯片将处理过的细胞的基因表达与载体对照的基因表达进行了比较。通过基因表达谱分析,我们鉴定出变化超过1.5倍的基因。转录组谱分析表明在媒介物对照和丁醛暴露组中不同的基因表达模式,并显示丁醛暴露组对基因改变的敏感性高于对照组。通过基因表达谱聚类分析,我们在丁醛IC5组中发现了2,998(上调1,379,下调了1,619),在丁醛IC20组中发现了3200,在基因中(上调了1,369和1,831下调了),其中有2,710(上调了1,281,上​​调了1,429)下调)共同的特定基因。通过基因本体论(GO)分析,这些常见表达的基因报告了几个与DNA损伤反应有关的关键生物学过程,例如“凋亡调控”,“细胞增殖调控”,“免疫反应”,“炎症反应” ”。我们使用细胞分析证实了功能改变。

著录项

  • 来源
    《Molecular & Cellular Toxicology》 |2013年第1期|85-94|共10页
  • 作者单位

    Center for Integrated Risk Research Cellular and Molecular Toxicology Laboratory Korea Institute of Science Technology">(112);

    School of Public Health Korea University">(212);

    Center for Integrated Risk Research Cellular and Molecular Toxicology Laboratory Korea Institute of Science Technology">(112);

    Center for Integrated Risk Research Cellular and Molecular Toxicology Laboratory Korea Institute of Science Technology">(112);

    School of Public Health Korea University">(212);

    Center for Integrated Risk Research Cellular and Molecular Toxicology Laboratory Korea Institute of Science Technology">(112);

    School of Public Health Korea University">(212);

    Center for Integrated Risk Research Cellular and Molecular Toxicology Laboratory Korea Institute of Science Technology">(112);

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Aldehyde; Butanal; Microarray; DNA damage; Apoptosis; Gene Ontology (GO); Kyoto Encyclopaedia of Genes and Genomes (KEGG) pathway;

    机译:醛;丁醛;微阵列;DNA损伤;细胞凋亡;基因本体论(GO);京都基因与基因组百科全书(KEGG)途径;

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