首页> 外文期刊>Journal of Toxicology and Environmental Health, Part A: Current Issues >Comparison of Gene Expression Profiles Induced By Coarse, Fine, and Ultrafine Particulate Matter
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Comparison of Gene Expression Profiles Induced By Coarse, Fine, and Ultrafine Particulate Matter

机译:粗,细和超细颗粒物质诱导的基因表达谱的比较

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Coarse, fine, and ultrafine particulate matter (PM) fractions possess different physical properties and chemical compositions and may produce different adverse health effects. Studies were undertaken to determine whether or not gene expression patterns may be used to discriminate among the three size fractions. Airway epithelial cells obtained from 6 normal individuals were exposed to Chapel Hill coarse, fine or ultrafine PM (250 μg/ml) for 6 and 24 h (n = 3 different individuals each). RNA was isolated and hybridized to Affymetrix cDNA microarrays. Significant genes were identified and mapped to canonical pathways. Expression of selected genes was confirmed by reverse-transcription polymerase chain reaction (RT-PCR). The numbers of genes altered by coarse, fine, and ultrafine PM increased from 0, 6, and 17 at 6 h to 1281, 302, and 455 at 24 h, respectively. The NRF2-mediated oxidative stress response, cell cycle:G2/M DNA damage checkpoint regulation, and mitotic roles of polo-like kinase were the top three pathways altered by all three fractions. Fine and ultrafine PM displayed more similar gene expression patterns. One example was the increased expression of metallothionein isoforms, reflecting the higher zinc content associated with fine and ultrafine fractions. A set of 10 genes was identified that could discriminate fine and ultrafine PM from coarse PM. These results indicate that common properties shared by the three size fractions as well as size-specific factors, e.g., compositions, may determine the effects on gene expression. Genomic markers may be used to discriminate coarse from fine and ultrafine PM.
机译:粗,细和超细颗粒物(PM)馏分具有不同的物理特性和化学组成,并可能产生不同的不良健康影响。进行了研究以确定基因表达模式是否可用于区分这三个大小部分。从6名正常人获得的气道上皮细胞暴露于Chapel Hill粗,细或超细PM(250μg/ ml)进行6和24小时(n = 3个人)。分离RNA并与Affymetrix cDNA微阵列杂交。确定了重要的基因,并将其定位于规范途径。通过逆转录聚合酶链反应(RT-PCR)确认所选基因的表达。被粗,细和超细颗粒物改变的基因数量分别从6小时的0、6和17增加到24小时的1281、302和455。 NRF2介导的氧化应激反应,细胞周期:G2 / M DNA损伤检查点调节和polo样激酶的有丝分裂作用是被这三个部分改变的最主要的三个途径。精细和超精细PM显示出更多相似的基因表达模式。一个例子是金属硫蛋白同工型的表达增加,反映出与细和超细级分相关的锌含量较高。确定了一组10个基因,可以区分粗粉和细粉。这些结果表明,三个大小部分共有的共同特性以及大小特异性因子(例如组成)可以决定对基因表达的影响。基因组标记物可用于区分粗粉和细粉。

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