首页> 美国卫生研究院文献>PLoS Clinical Trials >Generation of transgenic chickens expressing the human erythropoietin (hEPO) gene in an oviduct-specific manner: Production of transgenic chicken eggs containing human erythropoietin in egg whites
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Generation of transgenic chickens expressing the human erythropoietin (hEPO) gene in an oviduct-specific manner: Production of transgenic chicken eggs containing human erythropoietin in egg whites

机译:以输卵管特异性方式表达人促红细胞生成素(hEPO)基因的转基因鸡的产生:蛋清中含有人促红细胞生成素的转基因鸡卵的生产

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摘要

The transgenic chicken has been considered as a prospective bioreactor for large-scale production of costly pharmaceutical proteins. In the present study, we report successful generation of transgenic hens that lay eggs containing a high concentration of human erythropoietin (hEPO) in the ovalbumin. Using a feline immunodeficiency virus (FIV)-based pseudotyped lentivirus vector enveloped with G glycoproteins of the vesicular stomatitis virus, the replication-defective vector virus carrying the hEPO gene under the control of the chicken ovalbumin promoter was microinjected to the subgerminal cavity of freshly laid chicken eggs (stage X). Stable germline transmission of the hEPO transgene to the G1 progeny, which were non-mosaic and hemizygous for the hEPO gene under the ovalbumin promoter, was confirmed by mating of a G0 rooster with non-transgenic hens. Quantitative analysis of hEPO in the egg whites and in the blood samples taken from G1 transgenic chickens showed 4,810 ~ 6,600 IU/ml (40.1 ~ 55.0 μg/ml) and almost no detectable concentration, respectively, indicating tightly regulated oviduct-specific expression of the hEPO transgene. In terms of biological activity, there was no difference between the recombinant hEPO contained in the transgenic egg white and the commercially available counterpart, in vitro. We suggest that these results imply an important step toward efficient production of human cytokines from a transgenic animal bioreactor.
机译:转基因鸡被认为是大规模生产昂贵的药物蛋白的预期生物反应器。在本研究中,我们报告了成功产生卵母蛋白中含有高浓度人类促红细胞生成素(hEPO)的卵的转基因母鸡。使用包裹有水泡性口腔炎病毒G糖蛋白的基于猫免疫缺陷病毒(FIV)的假型慢病毒载体,在鸡卵白蛋白启动子的控制下,将携带hEPO基因的复制缺陷型载体病毒显微注射到刚产下的子皮腔内鸡蛋(X阶段)。通过将G0公鸡与非转基因母鸡交配,证实了hEPO转基因向g1子代的稳定种系传递是卵清蛋白启动子下hEPO基因的非镶嵌和半合子。从G1转基因鸡的蛋清和血液样品中对hEPO的定量分析分别显示4,810〜6,600 IU / ml(40.1〜55.0μg/ ml),几乎没有可检测到的浓度,表明该蛋白的输卵管特异性表达受到严格调节。 hEPO转基因。就生物学活性而言,在体外,转基因蛋白中所含的重组hEPO与市售对应物之间没有差异。我们建议这些结果意味着从转基因动物生物反应器高效生产人类细胞因子的重要一步。

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