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首页> 外文期刊>Archives of Toxicology >Activation of sterol regulatory element-binding proteins in mice exposed to perfluorooctanoic acid for 28 days
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Activation of sterol regulatory element-binding proteins in mice exposed to perfluorooctanoic acid for 28 days

机译:暴露于全氟辛酸28天的小鼠中固醇调节元件结合蛋白的激活

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Perfluoroalkyl acids are widely used in numerous industrial and commercial applications due to their unique physical and chemical characteristics. Although perfluorooctanoic acid (PFOA) is associated with hepatomegaly through peroxisome proliferator-activated receptor alpha (PPAR alpha) activation, liver fat accumulation and changes in gene expression related to fatty acid metabolism could still be found in PPAR alpha-null mice exposed to PFOA. To explore the potential effects of PFOA on sterol regulatory element-binding proteins (SREBPs) activity, male mice were dosed with either Milli-Q water or PFOA at doses of 0.08, 0.31, 1.25, 5, and 20 mg/kg/day by gavage for 28 days. Liver total cholesterol concentrations and PFOA contents showed a dose-dependent decrease and increase, respectively. Transcriptional activity of PPAR alpha and SREBPs was significantly enhanced in livers. Protein expression analyzed by Western blotting showed that PFOA exposure stimulated SREBP maturation. Furthermore, proteins blocked SREBP precursor transport, insulin-induced gene 1 (INSIG1) and INSIG2 proteins, as well as a protein-mediated nuclear SREBP proteolysis, F-box and WD-40 domain protein 7, decreased in mouse liver exposed to PFOA. The expression levels of the miR-183-96-182 cluster, which is possibly involved in a regulatory loop intermediated by SREBPs maturation, were also increased in the mouse liver after PFOA exposure. We also observed that PFOA induced lipid content and PPAR alpha in Hepa 1-6 cells after exposure to PFOA for 72 h but SREBPs were not activated in vitro. These results demonstrated that SREBPs were maturated by activating the miR-183-96-182 cluster-SREBP regulatory loop in PFOA-exposed mouse liver.
机译:全氟烷基酸由于其独特的物理和化学特性而被广泛用于许多工业和商业应用中。尽管全氟辛酸(PFOA)通过过氧化物酶体增殖物激活的受体α(PPARα)激活与肝肿大相关,但是在暴露于PFOA的PPARα空小鼠中仍可发现肝脂肪积累和与脂肪酸代谢相关的基因表达变化。为了探索PFOA对固醇调节元件结合蛋白(SREBPs)活性的潜在影响,通过给雄性小鼠服用Milli-Q水或PFOA,剂量为0.08、0.31、1.25、5和20 mg / kg /天。灌胃28天。肝脏总胆固醇浓度和PFOA含量分别呈剂量依赖性降低和升高。在肝脏中,PPARα和SREBP的转录活性显着增强。通过蛋白质印迹分析的蛋白质表达表明,PFOA暴露刺激了SREBP成熟。此外,在暴露于PFOA的小鼠肝脏中,蛋白质阻断了SREBP前体转运,胰岛素诱导的基因1(INSIG1)和INSIG2蛋白质,以及蛋白质介导的核SREBP蛋白质水解,F-box和WD-40域蛋白7减少。暴露于PFOA后,小鼠肝脏中miR-183-96-182簇的表达水平也可能增加,该水平可能参与SREBPs成熟介导的调节环。我们还观察到,暴露于PFOA 72 h后,PFOA诱导了Hepa 1-6细胞中的脂质含量和PPARα,但SREBP在体外没有被激活。这些结果表明,通过激活暴露于PFOA的小鼠肝脏中的miR-183-96-182簇-SREBP调节环,可以使SREBP成熟。

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