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Analysis of the miRNA Expression Profiles in the Zearalenone-Exposed TM3 Leydig Cell Line

机译:玉米赤霉烯酮暴露的TM3 Leydig细胞系中miRNA表达谱的分析

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摘要

Zearalenone (ZEN), an important environmental pollutant, can cause serious harm to human and animal health. The aim of our study was to examine the effect of zearalenone (ZEN) on miRNA expression profiles in the mouse Leydig cell line (TM3 Leydig cell line) by miRNA sequencing. The effect of ZEN on the viability of TM3 Leydig cells was verified by Cell Counting Kit-8 (CCK-8). MiRNA sequencing was performed 24 h after the exposure of TM3 Leydig cells with 50 μmol/L of ZEN. Bioinformatics predicted the miRNA target genes, performed Gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses, and conducted miRNA-gene-pathway mapping to show the relationship between miRNA, the target gene, and the signalling pathway. The expression levels of miRNA and the miRNA target genes associated with ZEN toxicology were verified by quantitative real-time polymerase chain reaction. The miRNA sequencing revealed a significant change (p < 0.05) in the 197 miRNAs in the ZEN-treated and control groups, among which 86 were up-regulated and 111 were down-regulated. GO analysis of the target genes of these miRNAs indicated various biological functions. KEGG analysis showed that the predicted miRNA target genes were involved in signalling pathways, such as cancer, apoptosis, and oxidation, namely, the Ras signalling pathway, Rap1 signalling pathway, PI3K-AKT signalling pathway, Foxo signalling pathway, and AMPK signalling pathway. These results suggest that ZEN, as an estrogen-like toxin, is regulated by microRNAs. Our results can help to examine the toxicological effects of ZEN-regulated miRNAs on germ cells.
机译:玉米赤霉烯酮(ZEN)是一种重要的环境污染物,会严重危害人类和动物健康。我们研究的目的是通过miRNA测序检查玉米赤霉烯酮(ZEN)对小鼠Leydig细胞系(TM3 Leydig细胞系)中miRNA表达谱的影响。 ZEN对TM3 Leydig细胞活力的影响已通过Cell Counting Kit-8(CCK-8)进行了验证。在TM3 Leydig细胞与50μmol/ L ZEN接触后24小时进行MiRNA测序。生物信息学预测了miRNA靶基因,进行了基因本体论(GO)和《京都议定书》的基因与基因组百科全书(KEGG)分析,并进行了miRNA-基因-途径映射,以显示miRNA,靶基因和信号通路之间的关系。通过定量实时聚合酶链反应验证了与ZEN毒理学相关的miRNA和miRNA靶基因的表达水平。 miRNA测序显示ZEN治疗组和对照组的197个miRNA有显着变化(p <0.05),其中86个上调而111个下调。这些miRNA的靶基因的GO分析表明各种生物学功能。 KEGG分析表明,预测的miRNA靶基因参与了癌症,细胞凋亡和氧化等信号通路,即Ras信号通路,Rap1信号通路,PI3K-AKT信号通路,Foxo信号通路和AMPK信号通路。这些结果表明,ZEN作为一种雌激素样毒素,受microRNA调控。我们的结果可以帮助检查ZEN调控的miRNA对生殖细胞的毒理作用。

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