首页> 美国卫生研究院文献>PLoS Clinical Trials >Proteomic changes of aryl hydrocarbon receptor (AhR)-silenced porcine granulosa cells exposed to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)
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Proteomic changes of aryl hydrocarbon receptor (AhR)-silenced porcine granulosa cells exposed to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)

机译:暴露于2,3,7,8-四氯二苯并-p-二恶英(TCDD)的芳烃受体(AhR)沉默的猪颗粒细胞的蛋白质组学变化

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摘要

2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) is a toxic man-made chemical compound contaminating the environment and affecting human/animal health and reproduction. Intracellular TCDD action usually involves the activation of aryl hydrocarbon receptor (AhR). The aim of the current study was to examine TCDD-induced changes in the proteome of AhR-silenced porcine granulosa cells. The AhR-silenced cells were treated with TCDD (100 nM) for 3, 12 or 24 h. Total protein was isolated, labeled with cyanines and next, the samples were separated by isoelectric focusing and SDS-PAGE. Proteins of interest were identified by MALDI-TOF/TOF mass spectrometry (MS) analysis and confirmed by western blotting and fluorescence immunocytochemistry. The AhR-targeted siRNA transfection reduced the granulosal expression level of AhR by 60–70%. In AhR-silenced porcine granulosa cells, TCDD influenced the abundance of only three proteins: annexin V, protein disulfide isomerase and ATP synthase subunit beta. The obtained results revealed the ability of TCDD to alter protein abundance in an AhR-independent manner. This study offers a new insight into the mechanism of TCDD action and provide directions for future functional studies focused on molecular effects exerted by TCDD.
机译:2,3,7,8-四氯二苯并-对二恶英(TCDD)是一种有毒的化学化合物,污染环境并影响人类/动物的健康和繁殖。细胞内TCDD的作用通常涉及芳烃受体(AhR)的激活。本研究的目的是检查TCDD诱导的AhR沉默的猪颗粒细胞蛋白质组的变化。将经AhR沉默的细胞用TCDD(100 nM)处理3、12或24小时。分离总蛋白,用花青素标记,然后通过等电聚焦和SDS-PAGE分离样品。目的蛋白通过MALDI-TOF / TOF质谱(MS)分析进行鉴定,并通过蛋白质印迹和荧光免疫细胞化学进行确认。以AhR为靶点的siRNA转染可将AhR的颗粒表达水平降低60-70%。在AhR沉默的猪颗粒细胞中,TCDD仅影响三种蛋白质的丰度:膜联蛋白V,蛋白质二硫键异构酶和ATP合酶β亚基。获得的结果揭示了TCDD以独立于AhR的方式改变蛋白质丰度的能力。这项研究为TCDD的作用机理提供了新的见解,并为今后针对TCDD发挥的分子作用的功能研究提供了指导。

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