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首页> 外文期刊>Tissue engineering, Part A >Adipose-derived stem cells promote angiogenesis and tissue formation for in vivo tissue engineering
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Adipose-derived stem cells promote angiogenesis and tissue formation for in vivo tissue engineering

机译:脂肪干细胞促进体内组织工程中的血管生成和组织形成

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Adult mesenchymal stem cells secrete a variety of angiogenic cytokines and growth factors, so we proposed that these paracrine mechanisms may be used to promote vascularization and growth for tissue engineering in vivo. We tested whether or not human adipose-derived stem cells (ASCs) promote tissue formation in rats. ASCs were evaluated in vitro for mRNA expression of angiogenic factors, including the vascular endothelial growth factor, basic fibroblast growth factor, interleukin-8 (IL-8), and stromal cell-derived factor-1 (SDF-1) and proliferative activity on human microvascular endothelial cells. For in vivo analysis, CM-DiI-labeled ASCs were implanted with a rat cardiac extracellular matrix (ECM) extract-derived hydrogel into a chamber with a femoral arteriovenous loop in the groin of male nude rats for 7 days. Vascularization in newly generated tissue was estimated by histomorphometry after endothelial nitric oxide synthase (eNOS) immunostaining. ASCs expressed growth factor mRNA and produced an angiogenic activity in vitro. After implantation, ASCs survived, but remained suspended in the ECM and relatively few were incorporated into the newly formed tissue. The volume of newly generated tissue was significantly higher in chambers containing ASCs and it was enriched with vasculature when compared with the ECM alone. We conclude that human ASCs promote tissue growth and angiogenesis in the rat vascularized chamber, thereby showing promise for tissue-engineering applications for regenerative therapy.
机译:成人间充质干细胞分泌多种血管生成细胞因子和生长因子,因此我们提出这些旁分泌机制可用于促进体内组织工程的血管生成和生长。我们测试了人类脂肪来源的干细胞(ASC)是否能促进大鼠的组织形成。体外评估ASCs的血管生成因子的mRNA表达,包括血管内皮生长因子,碱性成纤维细胞生长因子,白介素8(IL-8)和基质细胞衍生因子1(SDF-1)以及其增殖活性。人微血管内皮细胞。为了进行体内分析,将大鼠心脏细胞外基质(ECM)提取物衍生的水凝胶植入CM-DiI标记的ASC中,在雄性裸鼠腹股沟中的股动静脉回路中植入7天。内皮一氧化氮合酶(eNOS)免疫染色后,通过组织形态计量学估计新生组织中的血管化。 ASC表达生长因子mRNA并在体外产生血管生成活性。植入后,ASC幸存下来,但仍悬浮在ECM中,并且相对较少的被掺入到新形成的组织中。与单独的ECM相比,在包含ASC的腔室中,新生成的组织的体积明显更高,并且其血管系统丰富。我们得出的结论是,人类ASC促进大鼠血管化腔室中的组织生长和血管生成,从而为再生疗法的组织工程应用显示出希望。

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