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Tris(1,3-dichloro-2-propyl) phosphate perturbs the expression of genes involved in immune response and lipid and steroid metabolism in chicken embryos

机译:磷酸三(1,3-二氯-2-丙基)酯干扰鸡胚免疫应答以及脂质和类固醇代谢相关基因的表达

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We previously demonstrated that in ovo exposure to the flame retardant tris(1,3-dichloro-2-propyl) phosphate (TDCPP) decreased plasma thyroxine levels, reduced growth parameters, and decreased gallbladder size in chicken embryos. In the current study DNA microarrays were used to evaluate global mRNA expression in liver tissue of male chicken embryos that exhibited the above mentioned effects. Injected doses were dimethyl sulfoxide vehicle control, 7.6 or 45. μg TDCPP/g egg. TDCPP caused significant changes in the expression of five genes at the low dose and 47 genes at the high dose (False Discovery Rate p≤. 0.1, fold change. ≥. 1.5). The gene expression analysis suggested a compromised immune function, a state of cholestatic liver/biliary fibrosis, and disrupted lipid and steroid metabolism. Circulating bile acid levels were elevated, which is an indication of liver dysfunction, and plasma cholesterol levels were reduced; however, hepatic bile acid and cholesterol levels were unaltered. Interactome analyses identified apolipoprotein E, hepatocyte nuclear factor 4 alpha, and peroxisome proliferator-activated receptor alpha as key regulatory molecules involved in the effects of TDCPP. Our results demonstrate a targeted effect of TDCPP toxicity on lipid metabolism, including cholesterol, that helps explain the aforementioned phenotypic effects, as chicken embryos are highly dependent on yolk lipids for growth and maintenance throughout development. Finally, our results are in concordance with the literature that describes TDCPP as a cancer-causing agent, since the majority of dysregulated genes were involved in cancer pathways.
机译:我们以前证明了在卵内暴露于阻燃剂三(1,3-二氯-2-丙基)磷酸三酯(TDCPP)会降低鸡胚血浆甲状腺素水平,降低生长参数并降低胆囊大小。在当前的研究中,DNA微阵列被用于评估表现出上述效应的雄性鸡胚肝脏组织中的整体mRNA表达。注射剂量为二甲基亚砜媒介物对照,7.6或45.μgTDCPP / g鸡蛋。 TDCPP导致低剂量的5个基因和高剂量的47个基因的表达发生了显着变化(假发现率p≤。0.1,倍数变化。≥。1.5)。基因表达分析表明免疫功能受损,胆汁淤积性肝/胆纤维化状态以及脂质和类固醇代谢中断。循环胆汁酸水平升高,表明肝功能异常,血浆胆固醇水平降低;但是,肝胆汁酸和胆固醇水平未改变。 Interactome分析确定了载脂蛋白E,肝细胞核因子4α和过氧化物酶体增殖物激活的受体α是参与TDCPP作用的关键调节分子。我们的结果表明TDCPP毒性对脂质代谢(包括胆固醇)有针对性的作用,这有助于解释上述表型作用,因为鸡胚高度依赖蛋黄脂来生长和维持整个发育。最后,我们的结果与描述TDCPP为致癌因子的文献相吻合,因为大多数失调的基因都参与了癌症的传播途径。

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