Long-term exposure to diesel exhaust particles induces concordant changes in DNA methylation and transcriptome in human adenocarcinoma alveolar basal epithelial cells.

IF 4.2 2区 生物学 Q1 GENETICS & HEREDITY Epigenetics & Chromatin Pub Date : 2024-08-05 DOI:10.1186/s13072-024-00549-3
Alexandra Lukyanchuk, Naomi Muraki, Tomoko Kawai, Takehiro Sato, Kenichiro Hata, Tsuyoshi Ito, Atsushi Tajima
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Abstract

Background: Diesel exhaust particles (DEP), which contain hazardous compounds, are emitted during the combustion of diesel. As approximately one-third of the vehicles worldwide use diesel, there are growing concerns about the risks posed by DEP to human health. Long-term exposure to DEP is associated with airway hyperresponsiveness, pulmonary fibrosis, and inflammation; however, the molecular mechanisms behind the effects of DEP on the respiratory tract are poorly understood. Such mechanisms can be addressed by examining transcriptional and DNA methylation changes. Although several studies have focused on the effects of short-term DEP exposure on gene expression, research on the transcriptional effects and genome-wide DNA methylation changes caused by long-term DEP exposure is lacking. Hence, in this study, we investigated transcriptional and DNA methylation changes in human adenocarcinoma alveolar basal epithelial A549 cells caused by prolonged exposure to DEP and determined whether these changes are concordant.

Results: DNA methylation analysis using the Illumina Infinium MethylationEPIC BeadChips showed that the methylation levels of DEP-affected CpG sites in A549 cells changed in a dose-dependent manner; the extent of change increased with increasing dose reaching the statistical significance only in samples exposed to 30 µg/ml DEP. Four-week exposure to 30 µg/ml of DEP significantly induced DNA hypomethylation at 24,464 CpG sites, which were significantly enriched for DNase hypersensitive sites, genomic regions marked by H3K4me1 and H3K27ac, and several transcription factor binding sites. In contrast, 9,436 CpG sites with increased DNA methylation levels were significantly overrepresented in genomic regions marked by H3K27me3 as well as H3K4me1 and H3K27ac. In parallel, gene expression profiling by RNA sequencing demonstrated that long-term exposure to DEP altered the expression levels of 2,410 genes, enriching 16 gene sets including Xenobiotic metabolism, Inflammatory response, and Senescence. In silico analysis revealed that the expression levels of 854 genes correlated with the methylation levels of the DEP-affected cis-CpG sites.

Conclusions: To our knowledge, this is the first report of genome-wide transcriptional and DNA methylation changes and their associations in A549 cells following long-term exposure to DEP.

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长期暴露于柴油废气颗粒会诱导人类腺癌肺泡基底上皮细胞的 DNA 甲基化和转录组发生一致的变化。
背景:柴油燃烧时会排放出含有有害化合物的柴油废气微粒(DEP)。由于全球约有三分之一的车辆使用柴油,人们越来越关注柴油废气对人体健康造成的风险。长期暴露于 DEP 与气道高反应性、肺纤维化和炎症有关;然而,人们对 DEP 影响呼吸道背后的分子机制知之甚少。可以通过研究转录和 DNA 甲基化的变化来了解这些机制。虽然已有多项研究关注了短期暴露于 DEP 对基因表达的影响,但有关长期暴露于 DEP 所引起的转录效应和全基因组 DNA 甲基化变化的研究还很缺乏。因此,在本研究中,我们调查了长期暴露于 DEP 引起的人腺癌肺泡基底上皮 A549 细胞的转录和 DNA 甲基化变化,并确定这些变化是否一致:使用Illumina Infinium MethylationEPIC BeadChip芯片进行的DNA甲基化分析表明,A549细胞中受DEP影响的CpG位点的甲基化水平以剂量依赖的方式发生变化;变化程度随着剂量的增加而增加,只有在暴露于30 µg/ml DEP的样本中才达到统计学意义。暴露于30微克/毫升的DEP四周后,24,464个CpG位点的DNA低甲基化被显著诱导,这些位点明显富集于DNase超敏位点、H3K4me1和H3K27ac标记的基因组区域以及几个转录因子结合位点。相比之下,DNA 甲基化水平增加的 9,436 个 CpG 位点在以 H3K27me3 以及 H3K4me1 和 H3K27ac 标记的基因组区域中的比例明显偏高。与此同时,通过 RNA 测序进行的基因表达谱分析表明,长期暴露于 DEP 会改变 2,410 个基因的表达水平,丰富了 16 个基因集,包括 Xenobiotic metabolism、Inflammatory response 和 Senescence。硅学分析表明,854 个基因的表达水平与受 DEP 影响的顺式-CpG 位点的甲基化水平相关:据我们所知,这是首次报道 A549 细胞长期暴露于 DEP 后的全基因组转录和 DNA 甲基化变化及其相关性。
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来源期刊
Epigenetics & Chromatin
Epigenetics & Chromatin GENETICS & HEREDITY-
CiteScore
7.00
自引率
0.00%
发文量
35
审稿时长
1 months
期刊介绍: Epigenetics & Chromatin is a peer-reviewed, open access, online journal that publishes research, and reviews, providing novel insights into epigenetic inheritance and chromatin-based interactions. The journal aims to understand how gene and chromosomal elements are regulated and their activities maintained during processes such as cell division, differentiation and environmental alteration.
期刊最新文献
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