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Comparative analysis of mesenchymal stromal cells from different tissue sources in respect to articular cartilage tissue engineering

机译:来自不同组织来源的间充质基质细胞在关节软骨组织工程方面的比较分析

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摘要

The main goal of this study was a comparison of biological properties of mesenchymal stromal cells (MSCs) obtained from bone marrow, adipose tissue and umbilical cord with respect to articular cartilage regeneration. MSCs were isolated and expanded in vitro up to the third passage. The kinetics of proliferation was analyzed by cell analyzer CEDEX XS and expression of selected markers was assessed by flow cytometry. The morphology was analyzed by inverted microscope and TEM. Pellet culture system and chondrogenic medium containing TGF-beta 1 was used to induce chondrogenic differentiation. Chondrogenesis was analyzed by real-time PCR; the expression of collagen type I and type II was compared. MSCs from all sources showed similar kinetics of proliferation and shared expression of CD73, CD90 and CD105; and were negative for CD14, CD20, CD34 and CD45. Observation under inverted microscope and TEM showed similar morphology of all analyzed MSCs. Cells from all sources underwent chondrogenic differentiation - they expressed collagen type II and acid mucopolysaccharides typical for hyaline cartilage. On the basis of obtained results it should be emphasized that MSCs from bone marrow, adipose tissue and umbilical cord share biological properties. They possess the chondrogenic potential and may be utilized in cartilage tissue engineering.
机译:这项研究的主要目的是比较从骨髓,脂肪组织和脐带获得的间充质基质细胞(MSCs)在关节软骨再生方面的生物学特性。分离MSC并在体外扩增直至第三代。通过细胞分析仪CEDEX XS分析增殖的动力学,并通过流式细胞术评估所选标记的表达。通过倒置显微镜和TEM分析形态。使用颗粒培养系统和含TGF-β1的软骨形成培养基诱导软骨形成分化。通过实时PCR分析软骨形成;比较I型和II型胶原蛋白的表达。来自所有来源的MSC显示相似的增殖动力学,并共同表达CD73,CD90和CD105。且CD14,CD20,CD34和CD45均为阴性。倒置显微镜和TEM观察表明,所有分析的MSC的形态相似。来自所有来源的细胞都经历了软骨分化-它们表达了II型胶原蛋白和透明质酸软骨典型的酸性粘多糖。在获得的结果的基础上,应该强调的是,来自骨髓,脂肪组织和脐带的MSC具有生物学特性。它们具有软骨形成的潜力,可用于软骨组织工程。

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