首页> 外文期刊>Macromolecular Symposia >Enhanced Collagen Type IV Based Differentiation of Embryonic Stem Cells Towards Flk-1 Expressing Vascular Progenitors by the Wnt/β-Catenin Synergist QS11
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Enhanced Collagen Type IV Based Differentiation of Embryonic Stem Cells Towards Flk-1 Expressing Vascular Progenitors by the Wnt/β-Catenin Synergist QS11

机译:Wnt /β-连环蛋白增效剂QS11增强的基于IV型胶原的胚胎干细胞向表达Flk-1的血管祖细胞的分化。

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摘要

Mouse embryonic stem (mES) cells when plated onto collagen type IV in the presence of serum-containing medium differentiate into a mixed cell population that contains low levels of Flk-1 expressing vascular progenitor cells. When isolated and re-plated onto collagen type IV, Flk-1+ cells further differentiate into PECAM1+ endothelial and SMA+ mural cells. However, the low abundance and transient nature by which Flk-1+ cells are generated during embryonic stem (ES) cell differentiation presents limitations in case large numbers of Flk-1+ cells or its derivates are to be obtained. To optimize Flk-1 progenitor induction from undifferentiated mES cells, the effects of QS11, a small organic molecule that synergistically activates canonical Wnt signalling, were investigated. In the presence of QS11 the percentage of Flk-1+ cells in differentiating cultures of mES cells increases 1.5 fold. Furthermore, QS11 enhances cell proliferation in differentiating mES cells that results in a 2 fold increase in cell numbers when Flk-1 induction is maximal. The combined effects of QS11 on differentiation and proliferation increase the efficiency by which Flk-1 progenitors can be generated by approximately 300%, thereby providing a novel tool for vascular progenitor cell production for use in fundamental research and applications such as tissue engineering.
机译:当在含血清的培养基中将小鼠胚胎干(mES)细胞铺在IV型胶原上时,它们分化成包含低水平Flk-1表达血管祖细胞的混合细胞群。当分离并重新铺在IV型胶原上时,Flk-1 +细胞会进一步分化为PECAM1 +内皮细胞和SMA +壁画细胞。但是,在要获得大量Flk-1 +细胞或其衍生物的情况下,胚胎干(ES)细胞分化过程中产生Flk-1 +细胞的低丰度和短暂性会带来局限性。为了优化未分化mES细​​胞的Flk-1祖细胞诱导,研究了QS11(一种协同激活经典Wnt信号的有机小分子)的作用。在存在QS11的情况下,mES细胞分化培养物中Flk-1 +细胞的百分比增加了1.5倍。此外,当Flk-1诱导最大时,QS11增强了分化的mES细胞中的细胞增殖,导致细胞数量增加了2倍。 QS11对分化和增殖的综合影响将Flk-1祖细胞的生成效率提高了约300%,从而为用于血管祖细胞的生产提供了一种新颖的工具,可用于基础研究和组织工程等应用。

著录项

  • 来源
    《Macromolecular Symposia》 |2011年第1期|p.236-243|共8页
  • 作者单位

    Biomaterials Science and Technology (BST), MIRA – Institute for Biomedical Technology and Technical Medicine, Faculty of Science and Technology, University of Twente;

    P.O. Box 217, 7500 AE Enschede, The Netherlands;

    Biomaterials Science and Technology (BST), MIRA – Institute for Biomedical Technology and Technical Medicine, Faculty of Science and Technology, University of Twente;

    P.O. Box 217, 7500 AE Enschede, The Netherlands;

    Biomaterials Science and Technology (BST), MIRA – Institute for Biomedical Technology and Technical Medicine, Faculty of Science and Technology, University of Twente;

    P.O. Box 217, 7500 AE Enschede, The Netherlands;

    Polymer Chemistry and Biomaterials (PBM), MIRA – Institute for Biomedical Technology and Technical Medicine, Faculty of Science and Technology, University of Twente;

    P.O. Box 217, 7500 AE Enschede, The Netherlands;

    Biomaterials Science and Technology (BST), MIRA – Institute for Biomedical Technology and Technical Medicine, Faculty of Science and Technology, University of Twente;

    P.O. Box 217, 7500 AE Enschede, The Netherlands;

    Faculty of Science and Technology, University of Twente, P.O. Box 217, 7500 AE Enschede, The Netherlands;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    collagen type IV; endothelial cell; Flk-1; mouse ES cells; mural cell; QS11; tissue engineering; vascular progenitor; Wnt/β-catenin pathway;

    机译:IV型胶原;内皮细胞;Flk-1;小鼠ES细胞;壁细胞;QS11;组织工程;血管祖细胞;Wnt /β-catenin途径;

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