体外转染成纤维细胞克隆猪绿色荧光蛋白的转基因表达及种系传播。

Dario Brunetti, Andrea Perota, Irina Lagutina, Silvia Colleoni, Roberto Duchi, Fiorella Calabrese, Michela Seveso, Emanuele Cozzi, Giovanna Lazzari, Franco Lucchini, Cesare Galli
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引用次数: 56

摘要

由于解剖学和生理学的原因,猪代表了未来人类器官移植的异种供体选择。然而,为了绕过几个免疫屏障,必须在猪的器官中出现强大而稳定的人类基因表达。本研究采用体外转染培养细胞结合体细胞核移植(SCNT)的方法建立了转基因猪,以评估pCAGGS载体在不同选择器存在下的普遍转基因表达。无论使用何种选择器,pCAGGS都被证实是一种非常有效的无处不在的转基因表达载体。绿色荧光蛋白(GFP)在转染的成纤维细胞中的表达也在核移植后,通过植入前和植入后的发育,在出生和成年期间保持不变。证实了该转基因基因在不沉默的情况下进行种系传播。GFP在包括内皮细胞在内的几种组织中普遍表达,因此它是一种不需要组织特异性的多种异种移植相关基因表达的合适载体。最后在成纤维细胞中共转染绿色和红色荧光蛋白转基因,核移植后获得表达两种荧光蛋白的囊胚。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Transgene expression of green fluorescent protein and germ line transmission in cloned pigs derived from in vitro transfected adult fibroblasts.

The pig represents the xenogeneic donor of choice for future organ transplantation in humans for anatomical and physiological reasons. However, to bypass several immunological barriers, strong and stable human genes expression must occur in the pig's organs. In this study we created transgenic pigs using in vitro transfection of cultured cells combined with somatic cell nuclear transfer (SCNT) to evaluate the ubiquitous transgene expression driven by pCAGGS vector in presence of different selectors. pCAGGS confirmed to be a very effective vector for ubiquitous transgene expression, irrespective of the selector that was used. Green fluorescent protein (GFP) expression observed in transfected fibroblasts was also maintained after nuclear transfer, through pre- and postimplantation development, at birth and during adulthood. Germ line transmission without silencing of the transgene was demonstrated. The ubiquitous expression of GFP was clearly confirmed in several tissues including endothelial cells, thus making it a suitable vector for the expression of multiple genes relevant to xenotransplantation where tissue specificity is not required. Finally cotransfection of green and red fluorescence protein transgenes was performed in fibroblasts and after nuclear transfer blastocysts expressing both fluorescent proteins were obtained.

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