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Generation of multidrug resistant human tissues by overexpression of the ABCG2 multidrug transporter in embryonic stem cells

机译:通过在胚胎干细胞中过度表达ABCG2多药转运蛋白来产生多药耐药性人体组织

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摘要

The ABCG2 multidrug transporter provides resistance against various endo- and xenobiotics, and protects the stem cells against toxins and stress conditions. We have shown earlier that a GFP-tagged version of ABCG2 is fully functional and may be used to follow the expression, localization and function of this transporter in living cells. In the present work we have overexpressed GFP-ABCG2, driven by a constitutive (CAG) promoter, in HUES9 human embryonic stem cells. Stem cell clones were generated to express the wild-type and a substrate-mutant (R482G) GFP-ABCG2 variant, by using the Sleeping Beauty transposon system. We found that the stable overexpression of these transgenes did not change the pluripotency and growth properties of the stem cells, nor their differentiation capacity to hepatocytes or cardiomyocytes. ABCG2 overexpression provided increased toxin resistance in the stem cells, and protected the derived cardiomyocytes against doxorubicin toxicity. These studies document the potential of a stable ABCG2 expression for engineering toxin-resistant human pluripotent stem cells and selected stem cell derived tissues.
机译:ABCG2多药转运蛋白可抵抗各种内源性和异源性生物,并保护干细胞免受毒素和压力条件的侵害。前面我们已经证明,带有ABTC2的GFP标签是完全功能性的,可以用来追踪该转运蛋白在活细胞中的表达,定位和功能。在目前的工作中,我们在HUES9人胚胎干细胞中由组成型(CAG)启动子驱动的GFP-ABCG2过表达。通过使用Sleeping Beauty转座子系统,生成了干细胞克隆以表达野生型和底物突变(R482G)GFP-ABCG2变体。我们发现这些转基因的稳定过表达并没有改变干细胞的多能性和生长特性,也没有改变它们对肝细胞或心肌细胞的分化能力。 ABCG2过表达在干细胞中提供了更高的毒素抗性,并保护了衍生的心肌细胞免受阿霉素的毒性。这些研究证明了稳定的ABCG2表达对于工程化抗毒素人多能干细胞和选定的干细胞衍生组织的潜力。

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