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首页> 外文期刊>Biomacromolecules >Tenascin-C Mimetic Peptide Nanofibers Direct Stem Cell Differentiation to Osteogenic Lineage
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Tenascin-C Mimetic Peptide Nanofibers Direct Stem Cell Differentiation to Osteogenic Lineage

机译:tenascin-c模拟肽纳料直接茎细胞分化与成骨谱系

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摘要

Extracellular matrix contains various signals for cell surface receptors that regulate cell fate through modulation of cellular activities such as proliferation and differentiation. Cues from extracellular matrix components can be used for development of new materials to control the stem cell fate. In this study, we achieved control of stem cell fate toward osteogenic commitment by using a single extracellular matrix element despite the contradictory effect of mechanical stiffness. For this purpose, we mimicked bone extracellular matrix by incorporating functional sequence of fibronectin type III domain from native tenascin-C on self-assembled peptide nanofibers. When rat mesenchymal stem cells (rMSCs) were cultured on these peptide nanofibers, alkaline phosphatase (ALP) activity and alizarin red staining indicated osteogenic differentiation even in the absence of osteogenic supplements. Moreover, expression levels of osteogenic marker genes were significantly enhanced revealed by quantitative real-time polymerase chain reaction (qRT-PCR), which showed the remarkable bioactive role of this nanofiber system on osteogenic differentiation. Overall, these results showed that tenascin-C mimetic peptides significantly enhanced the attachment, proliferation, and osteogenic differentiation of rMSCs even in the absence of any external bioactive factors and regardless of the suitable stiff mechanical properties normally required for osteogenic differentiation. Thus, these peptide nanofibers provide a promising new platform for bone regeneration.
机译:细胞外基质含有用于细胞表面受体的各种信号,其通过调节细胞活性,例如增殖和分化等细胞生命运。细胞外基质组分的提示可用于开发新材料以控制干细胞命运。在这项研究中,尽管机械刚度的矛盾作用,但我们通过使用单个细胞外基质元素实现了对溶扰性承诺的控制。为此目的,通过在自组装肽纳米纤维上从天然Tenascin-C掺入纤连蛋白型III结构域的功能序列来模仿骨细胞外基质。当大鼠间充质干细胞(RMSC)在这些肽纳米纤维上培养时,即使在没有骨质原料补充剂的情况下,碱性磷酸酶(ALP)活性和茜素红染色表明骨质发生分化。此外,通过定量的实时聚合酶链反应(QRT-PCR)显着增强了骨质原性标记基因的表达水平,显示了该纳米纤维系统对成骨分化的显着生物活性作用。总体而言,这些结果表明,即使在没有任何外部生物活性因子的情况下,塔替辛蛋白-C的模拟肽也显着提高了RMSC的附着,增殖和骨质发生分化,并且不管骨质发生分化通常需要合适的刚性机械性能。因此,这些肽纳米纤维提供了一个有希望的骨再生平台。

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  • 来源
    《Biomacromolecules 》 |2014年第12期| 共8页
  • 作者单位

    Bilkent Univ Inst Mat Sci &

    Nanotechnol Natl Nanotechnol Res Ctr UNAM TR-06800 Ankara Turkey;

    Bilkent Univ Inst Mat Sci &

    Nanotechnol Natl Nanotechnol Res Ctr UNAM TR-06800 Ankara Turkey;

    Bilkent Univ Inst Mat Sci &

    Nanotechnol Natl Nanotechnol Res Ctr UNAM TR-06800 Ankara Turkey;

    Bilkent Univ Inst Mat Sci &

    Nanotechnol Natl Nanotechnol Res Ctr UNAM TR-06800 Ankara Turkey;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分子生物学 ;
  • 关键词

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