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首页> 外文期刊>Journal of tissue engineering and regenerative medicine >Enhanced tenogenic differentiation and tendon-like tissue formation by tenomodulin overexpression in murine mesenchymal stem cells
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Enhanced tenogenic differentiation and tendon-like tissue formation by tenomodulin overexpression in murine mesenchymal stem cells

机译:用鼠间充质干细胞的替补素过度表达增强遗传分化和肌腱样组织形成

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As a highly specific marker of tenocytes, tenomodulin (Tnmd) functions remain largely unexplored. We investigated the effect of Tnmd overexpression on tenogenic differentiation of murine mesenchymal stem cells (mMSCs) via plasmid-mediated overexpression in the C3H10T1/2 cell line. The results showed that overexpressed Tnmd could significantly enhance cell proliferation (p<0.05) and the gene expressions of tenogenic-related molecules, including Tnmd, Scleraxis (Scx), collagens I, III and VI and decorin (p<0.05), and significantly inhibit mMSCs differentiation towards the adipogenic, chondrogenic and osteogenic lineages (p<0.05). Upon in vivo implantation with rat tail collagen gel subcutaneously in nude mice, Tnmd-overexpressed C3H10T1/2 cells formed neotendon-like tissue, which revealed a histological feature of wave-like dense collagen fibres and cells aligned in parallel. By contrast, a disorganized connective tissue structure with randomly distributed cells was observed in the control group. To further confirm this finding, a conditional Tnmd-overexpressing mouse model was established and the derived primary mMSCs could be induced to overexpress Tnmd with>two-fold upregulated gene expression (p<0.05) by the treatment of doxycycline (Dox). Similarly, conditional overexpression of Tnmd in primary mMSCs also led to faster proliferation (p<0.05), enhanced gene expression of tenogenic markers (p<0.05) and the inhibited expressions of adipogenic and osteogenic markers (p<0.05). The results of enhanced tenogenic differentiation and neotendon formation indicated that Tnmd may serve not only as a tenogenic marker but also as a positive regulator of MSCs tenogenic differentiation, which might be applied to MSCs-mediated tendon regeneration. Copyright (C) 2016 John Wiley & Sons, Ltd.
机译:作为替尼细胞的高度特异性标记,替补素(TNMD)函数仍然很大程度上是未开发的。我们研究了TNMD过表达对鼠间充质干细胞(MMSCs)遗传分化的影响通过质粒介导的C3H10T1 / 2细胞中的过表达。结果表明,过表达的TNMD可以显着增强细胞增殖(P <0.05)和遗传相关分子的基因表达,包括TNMD,Scleraxis(SCX),胶原蛋白I,III和VI和DENDIN(P <0.05),并且显着抑制MMSCs朝向脂肪发生,软骨内和骨质发生谱系的分化(P <0.05)。在裸鼠中皮下植入大鼠尾胶原凝胶,TNMD-过度抑制的C3H10T1 / 2细胞形成了鼻顿样组织,揭示了波状致密胶原纤维的组织学特征和平行排列的细胞。相反,在对照组中观察到具有随机分布细胞的混乱结缔组织结构。为了进一步证实该发现,建立了条件TNMD过表达鼠标模型,通过治疗十氧环(DOX),可以诱导衍生的原发性MMSC与>双倍上调的基因表达(P <0.05)过表达TNMD。类似地,在一次MMSC中的TNMD的条件过表达也导致了更快的增殖(P <0.05),增强的胎生标记物的基因表达(P <0.05)和抑制表达脂肪和骨质形成标记物(P <0.05)。增强遗传分化和新生酮形成的结果表明,TNMD不仅可以作为遗传标记物而且作为MSCs遗传分化的阳性调节剂,这可能适用于MSC介导的肌腱再生。版权所有(c)2016 John Wiley&Sons,Ltd。

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