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Expression of Renal Genes in Mouse Embryonic Stem Cell Co-cultured with Fetal Renal cells

机译:肾脏基因在小鼠胚胎干细胞共培养中的表达胎儿肾细胞

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Embryonic stem(ES) cells co-cultured with different embryonic organic cells could differentiate into a broad spectrum of specialized cell types, including hepatocyte, cardiomyocyte and alveolar epithelial type II cell types. Such ES cells-derived cells can provide a valuable source of progenitor cell types, and could be a new source for cell transplantation. Here we imitate the embryonic kidney development microenvironment by co-culture the mouse ES cells with fetal renal cells, and the treated ES cells were detected expressing marker molecules characteristic for initiation of nephrogenesis (WT-1,emx-2and Wnt-4) and terminally differentiated renal cell types (podocalyxin,Nephl and RSOR). On the other side, the gene expressions of Oct-4, Nanog and Klf-4 were obviously depressed, which are associated with the ES cells' capacity to differentiate into all kinds of cells. In summary, the fetal renal microenvironment may lead the ES cells differentiate toward a renal lineage, especially the renal ancester cells, and such in vitro–generated cells may be very useful for the development of bioartificial organs or cell-based therapies in chronic or acute renal failure.
机译:与不同的胚胎有机细胞共培养的胚胎干细胞可以分化为多种专门细胞类型,包括肝细胞,心肌细胞和肺泡上皮II型细胞类型。此类ES细胞衍生的细胞可以提供有价值的祖细胞类型来源,并且可以成为细胞移植的新来源。在这里,我们通过将小鼠胚胎干细胞与胎儿肾细胞共培养来模拟胚胎肾脏发育的微环境,检测到处理过的胚胎干细胞表达了特征性标志物分子,这些标志物分子具有启动肾生成的特征性分子(WT-1,emx-2和Wnt-4)并最终表达分化的肾细胞类型(podocalyxin,Nephl和RSOR)。另一方面,Oct-4,Nanog和Klf-4的基因表达明显降低,这与ES细胞分化为各种细胞的能力有关。总之,胎儿肾微环境可能导致ES细胞向肾谱系分化,尤其是肾祖细胞,这种体外生成的细胞对于慢性或急性生物人工器官或基于细胞的疗法的发展可能非常有用。肾衰竭。

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