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Co-expressing Pdx1 and Ngn3 induces few beta-like cells in the liver of mice

机译:共表达Pdx1和Ngn3诱导小鼠肝脏中很少的β样细胞

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We have assessed whether expressing pancreatic transcription factors PdxI and Ngn3 in the liver could induce beta-like cells for curing type I diabetes. When co-expressed in the liver of insulin reporter mice using adenovirus, few cells in the liver were turned into betalike cells which were marked by lacZ expression by X-gal staining. Insulin promoter assay showed that Pdxl highly activates insulin promoter when combined with Ngn3. In ex vivo experiments to determine permissiveness of stem/progenitor and fully differentiated cells by ectopic transcription factors, it was found that more islet genes were induced in ES or bone marrow SP cells than fully differentiated NIH3T3 or MEF cells by PdxI or Ngn3. Our results suggest that synergistic action of PdxI and Ngn3 on inducing various islet genes as well as cell intrinsic factors played a crucial role in directing few liver cells into beta-like cells in vivo. (c) 2007 Elsevier Inc. All rights reserved.
机译:我们已经评估了在肝脏中表达胰腺转录因子PdxI和Ngn3是否可以诱导β样细胞治愈I型糖尿病。当使用腺病毒在胰岛素报告基因小鼠的肝脏中共表达时,肝脏中几乎没有细胞变成β样细胞,通过X-gal染色以lacZ表达为特征。胰岛素启动子测定表明,Pdxl与Ngn3结合时可高度活化胰岛素启动子。在通过异位转录因子确定干细胞/祖细胞和完全分化细胞的允许性的离体实验中,发现与PdxI或Ngn3完全分化的NIH3T3或MEF细胞相比,ES或骨髓SP细胞诱导的胰岛基因更多。我们的结果表明,PdxI和Ngn3在诱导各种胰岛基因以及细胞内在因子方面的协同作用在体内将少量肝细胞导入β样细胞中起着至关重要的作用。 (c)2007 Elsevier Inc.保留所有权利。

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