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首页> 外文期刊>Comparative biochemistry and physiology, Part A. Molecular and integrative physiology >Effects of estradiol-17 beta treatment on in vitro and in vivo synthesis of two distinct vitellogenins in tilapia
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Effects of estradiol-17 beta treatment on in vitro and in vivo synthesis of two distinct vitellogenins in tilapia

机译:雌二醇-17β处理对罗非鱼中两种不同卵黄蛋白原的体内外合成的影响

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Two distinct vitellogenins (VTG) were purified from the blood of estradiol-17 beta (E-2)-injected tilapia, Oreochromis mossambicus. Enzyme-linked immunosorbent assays (ELISA) of each VTG were developed to examine effects of E-2 treatment on induction of VTG synthesis in the primarily cultured tilapia hepatocytes. Two VTG molecules (VTG210 and VTG140) had apparent molecular masses of 370 and 220 kDa by gel filtration and 210 and 140 kDa by SDS-PAGE, respectively. Western blot analyses showed that antibodies raised against the purified VTG210 and VTG140 reacted only with each protein band. Furthermore, ELISA for each VTG was specific for target VTG. When E-2 was added into the media of primarily cultured tilapia hepatocytes, VTG210 and VTG140 were both detected from E-2 concentrations of 1 x 10(-7) M and 5 x 10(-7) M, respectively. Time course experiments showed that there was a difference in the detection time of VTG210 and VTG140 after the hormone treatment. Although the injection of different E-2 doses induced both VTGs in the plasma of male tilapia, the concentration of VTG210 was nearly five to eight times higher than that of VTG140. These results suggest that E-2 is a direct inducer of both VTGs in the tilapia hepatocytes in vitro and in vivo, and that there is difference in the hormone response in inducing the VTGs in the tilapia hepatocytes. (C) 2001 Elsevier Science Inc. All rights reserved. [References: 30]
机译:从注射了雌二醇17β(E-2)的罗非鱼(Oreochromis mossambicus)的血液中纯化了两种不同的卵黄蛋白原(VTG)。开发了每种VTG的酶联免疫吸附试验(ELISA),以检查E-2处理对主要培养的罗非鱼肝细胞中VTG合成的诱导作用。通过凝胶过滤,两个VTG分子(VTG210和VTG140)的表观分子量分别为370和220 kDa,通过SDS-PAGE分别为210和140 kDa。蛋白质印迹分析表明,针对纯化的VTG210和VTG140产生的抗体仅与每个蛋白条带反应。此外,每个VTG的ELISA对目标VTG具有特异性。当将E-2添加到主要培养的罗非鱼肝细胞培养基中时,分别从1 x 10(-7)M和5 x 10(-7)M的E-2浓度中检测到VTG210和VTG140。时程实验表明,激素处理后VTG210和VTG140的检测时间有所不同。尽管注射不同剂量的E-2会诱导雄性罗非鱼血浆中的两种VTG,但VTG210的浓度却比VTG140高出近五到八倍。这些结果表明,E-2是体外和体内罗非鱼肝细胞中两种VTG的直接诱导剂,并且在诱导罗非鱼肝细胞中的VTG方面激素反应存在差异。 (C)2001 Elsevier Science Inc.保留所有权利。 [参考:30]

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