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首页> 外文期刊>Cellular Physiology and Biochemistry >The Role of Chemokines in Proangiogenic Action Induced by Human Adipose Tissue-Derived Mesenchymal Stem Cells in the Murine Model of Hindlimb Ischemia
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The Role of Chemokines in Proangiogenic Action Induced by Human Adipose Tissue-Derived Mesenchymal Stem Cells in the Murine Model of Hindlimb Ischemia

机译:趋化因子在人脂肪组织间充质干细胞在后肢缺血小鼠模型中促血管生成作用中的作用。

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摘要

The proangiogenic action of human adipose tissue-derived mesenchymal stem cells (hASCs) transplantation has been shown to be mediated by secretory factors. In this study, we determined if human granulocyte chemotactic protein-2(GCP2) or monocyte chemoattractant protein-1(MCP1) is involved in the proangiogenic action of hASCs transplantation in the hindlimb ischemia model. hASCs secrete GCP2 and MCP1, which leads to increased tubule formation. The downregulation of GCP2 or MCP1 decreased MCP1 and GCP2 secretion, respectively, whereas the external addition of GCP2 or MCP1 increased MCP1 and GCP2, respectively. Additionally, the treatment of GCP2 and MCP1 increased VEGF secretion, while the downregulation of GCP2 and MCP1 showed the opposite effect on VEGF secretion. Downregulation of GCP2 and MCP1 expression also inhibited hASCs-induced proangiogenic action, while the overexpression of GCP2 increased it. Finally, the downregulation of MCP1 or VEGF inhibited the GCP2 overexpression-induced increase in blood flow recovery. Taken together, these data indicate that the proangiogenic action of hASCs transplantation is mediated by the interaction between GCP2, MCP1 and VEGF, which are secreted from the transplanted cells.
机译:人类脂肪组织间充质干细胞(hASCs)移植的促血管生成作用已被证明是由分泌因子介导的。在这项研究中,我们确定是否人类粒细胞趋化蛋白2(GCP2)或单核细胞趋化蛋白1(MCP1)参与了后肢缺血模型中hASCs移植的促血管生成作用。 hASC分泌GCP2和MCP1,从而导致肾小管形成增加。 GCP2或MCP1的下调分别减少了MCP1和GCP2的分泌,而外部添加GCP2或MCP1分别增加了MCP1和GCP2。此外,GCP2和MCP1的治疗可增加VEGF的分泌,而GCP2和MCP1的下调对VEGF的分泌却显示相反的作用。 GCP2和MCP1表达的下调也抑制了hASCs诱导的促血管生成作用,而GCP2的过表达则增加了它。最后,MCP1或VEGF的下调抑制了GCP2过表达诱导的血流恢复增加。综上所述,这些数据表明,hASCs移植的促血管生成作用是由移植细胞分泌的GCP2,MCP1和VEGF之间的相互作用介导的。

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