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Identification of differentially expressed genes by 2,3,7,8- tetrachlorodibenzo-p-dioxin in human bronchial epithelial cells

机译:2,3,7,8-四氯二苯并-p-二恶英在人支气管上皮细胞中鉴定差异表达基因

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摘要

Dioxin (2,3,7,8-tetrachlorodibenzo-p-dioxin; TCDD) is one of the most powerful environmental toxins and causes a variety of toxic effects in humans. Since it makes first contact with bronchial epithelial cells as an atmospheric contaminant, we identified differentially expressed genes (DEGs) in TCDD-treated human bronchial epithelial cells (HBE4-E6/E7) using an annealing control primer (ACP) system. Six genes, five upregulated and one downregulated, were isolated and their expression patterns were confirmed by reverse dot blot analysis. Their genomic sequences were used for identification, and the upregulated proteins were found to be acyl-coenzyme A dehydrogenase (VLCAD), S100 calcium binding protein A6 (S100A6), nuclear receptor co-repressor 2 (NCOR2), ribosomal protein, large, P1 (RPLP1), and tubulin α 1c, and the downregulated protein was shown to be tubulin β2. Among them, the expression of the S100A6 was further analysed by northern hybridization because of its relationship with TCDD. These results suggest that this new method was simple and convenient to identify DEGs regulated by a specific agent. Moreover, these isolated genes may provide important information to better understand the mechanisms of TCDD toxicity in human bronchial epithelial cells.
机译:二恶英(2,3,7,8-四氯二苯并-p-二恶英; TCDD)是最强大的环境毒素之一,对人类产生多种毒性作用。由于它首先与大气污染物接触支气管上皮细胞,因此我们使用退火控制引物(ACP)系统在TCDD处理的人支气管上皮细胞(HBE4-E6 / E7)中鉴定了差异表达的基因(DEG)。分离出六个基因,五个上调和一个下调,并通过反向斑点印迹分析证实了它们的表达模式。使用它们的基因组序列进行鉴定,发现上调的蛋白为酰基辅酶A脱氢酶(VLCAD),S100钙结合蛋白A6(S100A6),核受体共阻遏物2(NCOR2),核糖体蛋白,大,P1 (RPLP1)和微管蛋白α1c,而被下调的蛋白质显示为微管蛋白β2。其中,由于其与TCDD的关系,通过Northern杂交进一步分析了S100A6的表达。这些结果表明,这种新方法简单,方便,可以识别由特定药物调节的DEG。此外,这些分离的基因可能提供重要的信息,以更好地了解人支气管上皮细胞中TCDD毒性的机制。

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