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Hypoxia Inducible Factor-1 alpha Regulates the Migration of Bone Marrow Mesenchymal Stem Cells via Integrin alpha(4)

机译:缺氧诱导因子-1α通过整合素α调节骨髓间充质干细胞的迁移(4)

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摘要

Although hypoxic environments have been known to regulate the migratory ability of bone marrow-derived mesenchymal stem cells (BM-MSCs), which is a critical factor for maximizing the therapeutic effect, the underlying mechanisms remain unclear. Therefore, we aimed to confirm the effect of hypoxia-inducible factor-1 alpha (HIF-1 alpha) on the migration of BM-MSCs and to analyze the interaction between HIF-1 alpha and integrin-mediated signals. Hypoxia-activated HIF-1 alpha significantly increased BM-MSC migration. The expression of integrin alpha(4) was decreased in BM-MSCs by increased HIF-1 alpha under hypoxia, whereas the expression of Rho-associated kinase 1 (ROCK1) and Rac1/2/3 was increased. After downregulation of HIF-1 alpha by YC-1, which is an inhibitor of HIF-1 alpha BM-MSC migration was decreased via upregulation of integrin alpha(4) and downregulation of ROCK1 and Rac1/2/3. Knockdown of integrin alpha(4) by integrin alpha(4) siRNA (siITGA4) treatment increased BM-MSC migration by upregulation of ROCK1, Rac1/2/3, and matrix metalloproteinase-2 regardless of oxygen tension. Moreover, siITGA4 treatment increased HIF-1 alpha expression and augmented the translocation of HIF-1 alpha into the nucleus under hypoxia. Taken together, the alternative expression of HIF-1 alpha induced by microenvironment factors, such as hypoxia and integrin alpha(4), may regulate the migration of BM-MSCs. These findings may provide insights to the underlying mechanisms of BM-MSC migration for successful stem cell-based therapy.
机译:虽然已知缺氧环境调节骨髓衍生的间充质干细胞(BM-MSCs)的迁徙能力,这是最大化治疗效果的关键因素,下面的机制仍然不清楚。因此,我们旨在确认缺氧诱导因子-1α(HIF-1α)对BM-MSC的迁移的影响,并分析HIF-1α和整合蛋白介导的信号之间的相互作用。缺氧激活的HIF-1α显着增加了BM-MSC迁移。通过缺氧下的HIF-1α增加,BM-MSCs的整联素α(4)的表达在BM-MSC中降低,而RHO相关激酶1(ROCK1)和RAC1 / 2/3的表达增加。通过YC-1下调HIF-1αhif-1,这是HIF-1α的抑制剂,通过整合蛋白α(4)的上调和Rock1和Rac1 / 2/3的下调来降低HIF-1α-MSC迁移。整合蛋白α(4)通过整合蛋白α(4)siRNA(SIITGA4)治疗敲低rOCK1,RAC1 / 2/3和基质金属蛋白酶-2的BM-MSC迁移增加,无论氧气张力如何。此外,SIITGA4治疗增加了HIF-1α表达,并在缺氧下扩增了HIF-1α的易位。携带的微环境因子(如缺氧和整合素Alpha(4)诱导的HIF-1α的替代表达,可以调节BM-MSCs的迁移。这些发现可以为BM-MSC迁移的潜在机制提供洞察,以成功的基于干细胞的治疗。

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  • 来源
    《Stem cells international》 |2016年第3期|共11页
  • 作者单位

    CHA Univ Dept Biomed Sci Songnam 13488 South Korea;

    CHA Univ Dept Internal Med CHA Bundang Med Ctr Songnam 13496 South Korea;

    Dankook Univ Dept Nanobiomed Sci Cheonan Si 31116 South Korea;

    CHA Univ Dept Internal Med CHA Bundang Med Ctr Songnam 13496 South Korea;

    Catholic Univ Korea Catholic High Performance Cell Therapy Ctr Seoul 06591 South Korea;

    CHA Univ Dept Biomed Sci Songnam 13488 South Korea;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物工程学(生物技术);
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