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Retinoic acid induces Pdx1-positive endoderm in differentiating mouse embryonic stem cells.

机译:维甲酸在分化小鼠胚胎干细胞中诱导Pdx1阳性内胚层。

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We have generated an embryonic stem (ES) cell line in which sequences encoding green fluorescent protein (GFP) were targeted to the locus of the pancreatic-duodenal homeobox gene (Pdx1). Analysis of chimeric embryos derived from blastocyst injection of Pdx1(GFP/w) ES cells demonstrated that the pattern of GFP expression was consistent with that reported for the endogenous Pdx1 gene. By monitoring GFP expression during the course of ES cell differentiation, we have shown that retinoic acid (RA) can regulate the commitment of ES cells to form Pdx1(+) pancreatic endoderm. RA was most effective at inducing Pdx1 expression when added to cultures at day 4 of ES differentiation, a period corresponding to the end of gastrulation in the embryo. RT-PCR analysis showed that Pdx1-positive cells from day 8 cultures expressed the early endoderm markers Ptf1a, Foxa2, Hnf4alpha, Hnf1beta, and Hnf6, consistent with the notion that they corresponded to the early pancreatic endoderm present in the embryonic day 9.5 mouseembryo. These results demonstrate the utility of Pdx1(GFP/w) ES cells as a tool for monitoring the effects of factors that influence pancreatic differentiation from ES cells.
机译:我们已经生成了胚胎干(ES)细胞系,其中编码绿色荧光蛋白(GFP)的序列靶向胰腺-十二指肠同源盒基因(Pdx1)的基因座。对胚泡注射Pdx1(GFP / w)ES细胞衍生的嵌合胚胎的分析表明,GFP表达模式与报道的内源Pdx1基因一致。通过监测ES细胞分化过程中GFP的表达,我们已经表明,视黄酸(RA)可以调节ES细胞形成Pdx1(+)胰腺内胚层的承诺。当在ES分化的第4天将其添加到培养物中时,RA可以最有效地诱导Pdx1表达。 RT-PCR分析显示,第8天培养物中的Pdx1阳性细胞表达了早期内胚层标记物Ptf1a,Foxa2,Hnf4alpha,Hnf1beta和Hnf6,这与它们对应于胚胎第9.5天小鼠胚中存在的早期胰腺内胚层的观念一致。这些结果证明Pdx1(GFP / w)ES细胞作为一种工具,可用于监测影响胰腺细胞从ES细胞分化的因素的影响。

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