野生鸬鹚肝脏与培养肝细胞基因表达谱的比较

K. Nakayama, H. Sakai, S. Kitamura, A. Sudo, Eun-Young Kim, S. Tanabe, H. Iwata
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引用次数: 2

摘要

利用微阵列平台分析了野生鸬鹚(Phalacrocorax carbo)肝脏中的基因表达谱,并预测了持久性有机污染物(POPs)和新兴POPs的潜在毒性作用。然而,将微阵列技术应用于野生动物时,污染物积累与基因表达改变之间的因果关系很难明确。因此,本研究从野生鸬鹚胚胎中分离肝细胞,用2,3,7,8 -四氯二苯并-对二恶英(TCDD)或3,3 ',4,4 ',5 -五氯联苯(PCB 126)进行培养和处理。通过微阵列分析监测培养细胞中的基因表达谱,然后比较野生鸬鹚肝脏(体内)和培养细胞(体外)对二恶英的反应。培养的肝细胞明显表现出对TCDD或PCB 126暴露的反应,包括细胞色素p4501a基因的诱导。虽然微阵列上的15个基因在体内和体外试验中显示出相似的效应,表明这些基因可能直接受到二恶英暴露的影响,但其他基因在野生鸬鹚肝脏和培养细胞之间的反应不同。因此,我们比较了体内和体外测试中二恶英反应基因的“生物过程”基因本体(GO)术语。大多数注释的氧化石墨烯在肝脏和培养细胞中是共享的,这意味着二恶英的影响在两组之间是相似的。因此,从鸬鹚分离的细胞中进行基因表达谱分析可能有助于评估对野生种群的化学影响。
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Comparison of Gene Expression Profiles in the Liver and Cultured Hepatic Cells from Wild Common Cormorants
We have analyzed the gene expression profiles in the liver of wild common cormorants ( Phalacrocorax carbo ) using microarray platform, and have predicted the potential toxic effects of persistent organic pollutants ( POPs ) and emerging POPs. However, when apply-ing microarray technology to wild animals, it is quite difficult to clarify the cause-and-effect relationship between accumulated contaminants and gene expression alterations. Therefore, in the present study, we isolated liver cells from wild cormorant embryos, and the cells were cultured and treated with 2 , 3 , 7 , 8 -tetrachlorodibenzo- p -dioxin ( TCDD ) or 3 , 3 ', 4 , 4 ', 5 -pentachlorobiphenyl ( PCB 126). The gene expression profiles in the cultured cells were monitored by microarray analysis, and responses to dioxins were then compared between livers ( in vivo ) and cultured cells ( in vitro ) from wild cormorants. The cultured liver cells clearly exhibited responses to the exposure of TCDD or PCB 126 including induc-tions of cytochrome P 450 1 A genes. Whereas fifteen genes on the microarray showed similar effects between in vivo and in vitro tests, indicating that these genes might be affected directly by dioxin exposure, the responses of other genes were different between wild cormorant livers and cultured cells. Therefore, we compared the ‘ biological process ’ gene ontology ( GO ) terms of dioxin-responsive genes between in vivo and in vitro tests. The most of annotated GO terms were shared in the livers and cultured cells, implying that the effects by dioxins were similar between both groups. Thus, gene expression profiling in the cells isolated from cormorants might be useful for evaluating chemical effects on the wild population.
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