首页> 外文期刊>In Vitro Cellular and Developmental Biology. Animal: Journal of the Tissues Culture Association >Phospholipid hydroperoxide glutathione peroxidase gene is regulated via an estrogen and estrogen receptor signaling in cultured mouse fetuses.
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Phospholipid hydroperoxide glutathione peroxidase gene is regulated via an estrogen and estrogen receptor signaling in cultured mouse fetuses.

机译:磷脂氢过氧化物谷胱甘肽过氧化物酶基因是通过培养的小鼠胎儿中的雌激素和雌激素受体信号传导来调节的。

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Although it has been suggested that the transcription of phospholipid hydroperoxide glutathione peroxidase (PHGPx), an essential antioxidant selenoenzyme, may be affected by the estrogen state in mammals, the direct mechanism underlying the regulation of the PHGPx gene by estrogens in mammalian tissues remains to be clearly elucidated. In this study, we evaluated the expression of the PHGPx mRNA in cultured mouse fetuses (embryonic days 8.5-10.5) exposed to 17beta-estradiol (E(2); 0.1, 1, 10, 100, and 1,000 ng/ml); estrogen receptor (ER) agonists [propyl pyrazole triol (PPT, an ERalpha-selective ligand, 1 mul/ml) and diarylpropionitrile (DPN, an ERbeta-selective ligand, 1 mul/ml)]; and/or ER antagonist [ICI 182,780 (ICI, 1 mul/ml)] using a whole embryo culture system. E(2)-alone treatment significantly stimulated the expressions of both ERalpha and ERbeta mRNAs in all the cultured fetuses (p < 0.05), although the ERbeta mRNA levels were higher than ERalpha mRNA. PHGPx mRNA expression was significantly increased in all the fetuses treated with E(2) (1-1,000 ng/ml), PPT, and DPN (p < 0.05). Furthermore, pretreatment with ICI completely blocked the E(2)-induced PHGPx mRNA expression in the fetuses. In addition, the mRNA levels of cytosolic GPx, the other intracellular antioxidant selenoenzyme, did not differ significantly from the controls by an exposure to those agents. These results suggest that the PHGPx gene is regulated via an estrogen and ER signal pathway in the cultured mouse fetus.CAS Registry/EC Number/Name of Substance 0 (Estrogen Receptor alpha). 0 (Estrogen Receptor beta). 0 (Estrogens). 0 (Nitriles). 0 (Propionates). 0 (Pyrazoles). 0 (diarylpropionitrile). 0 (propyl pyrazole triol). 129453-61-8 (fulvestrant). 50-28-2 (Estradiol). 63231-63-0 (RNA). EC 1-11-1-12 (phospholipid-hydroperoxide glutathione peroxidase). EC 1-11-1-9 (Glutathione Peroxidase).
机译:尽管有人提出,一种重要的抗氧化剂硒酶磷脂氢过氧化物谷胱甘肽过氧化物酶(PHGPx)的转录可能受到哺乳动物雌激素状态的影响,但哺乳动物组织中雌激素调节PHGPx基因的直接机制仍然是明确阐明。在这项研究中,我们评估了暴露于17β-雌二醇(E(2); 0.1、1、10、100和1,000 ng / ml)的培养的小鼠胎儿(胚胎第8.5-10.5天)中PHGPx mRNA的表达;雌激素受体(ER)激动剂[丙基吡唑三醇(PPT,ERalpha选择性配体,1 mul / ml)和二芳基丙腈(DPN,ERbeta选择性配体,1 mul / ml)];和/或ER拮抗剂[ICI 182,780(ICI,1 mul / ml)]使用整个胚胎培养系统。单独的E(2)处理显着刺激了所有培养的胎儿中ERalpha和ERbeta mRNA的表达(p <0.05),尽管ERbeta mRNA的水平高于ERalpha mRNA。在用E(2)(1-1,000 ng / ml),PPT和DPN处理的所有胎儿中,PHGPx mRNA表达均显着增加(p <0.05)。此外,用ICI预处理完全阻断了胎儿体内E(2)诱导的PHGPx mRNA表达。此外,胞质GPx(其他细胞内抗氧化剂硒酶)的mRNA水平与对照组相比没有显着差异。这些结果表明,在培养的小鼠胎儿中,PHGPx基因是通过雌激素和ER信号途径调控的。CASRegistry / EC编号/物质名称0(雌激素受体α)。 0(雌激素受体beta)。 0(雌激素)。 0(腈)。 0(丙酸)。 0(吡唑)。 0(二芳基丙腈)。 0(丙基吡唑三醇)。 129453-61-8(fulvestrant)。 50-28-2(雌二醇)。 63231-63-0(RNA)。 EC 1-11-1-12(磷脂-氢过氧化物谷胱甘肽过氧化物酶)。 EC 1-11-1-9(谷胱甘肽过氧化物酶)。

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