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Human Adipose Stem Cells in Chondrogenic Differentiation Medium without Growth Factors Differentiate Towards Annulus Fibrosus Phenotype In Vitro

机译:人体脂肪干细胞在软骨中的分化介质中没有生长因子在体外分化朝向环纤维型表型分化

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Intervertebral disc degeneration is the main cause of chronic back pain. Disc degeneration mainly leads to tearing of annulus fibrosus (AF), which is with current methods difficult to restore and impossible to regenerate. Stem cell technology offers a potential technique to repair the ruptured AF by enabling new matrix synthesis at the defect site. Previous studies have shown that human adipose stem cells (hASCs) are able to differentiate towards AF phenotype when treated with suitable growth factors. There are concerns about the use of growth factors in clinical applications because of their short half-lives, high costs and low effectiveness. The main aim of this research project was to regenerate AF tissue in vitro using hASCs and serum free chondrogenic medium without supplementation of growth factors. Differentiation of hASCs was induced by using the micromass culture technique. Human annulus fibrosus cell (hAFCs) cultured in commercial AF growth medium were used as positive control. Assessment of AF phenotype of hASCs and hAFCs was done at 14 and 21 days of culture. Quantification of sulphated glycosaminoglycan (GAG) content showed that hASCs cultured in chondrogenic medium expressed similar levels of sulphated GAGs as hAFCs. qRT-PCR confirmed the similarity of the differentiated hASCs with AF phenotype. Several markers for AF phenotype (aggrecan, collagen type I and glypican-3) were expressed in both hAFCs and differentiated hASCs. This is the first study that demonstrated that hASCs can be differentiated towards AF phenotype using serum free chondrogenic medium without growth factors. In a next step, scaffolds manufactured from biodegradable polymers will be used in combination with ASCs to find an optimal construct to repair AF defects.
机译:椎间盘变性是慢性背痛的主要原因。盘变性主要导致环形纤维(AF)的撕裂,这与当前方法难以恢复,并且不可能再生。干细胞技术提供了一种通过在缺陷现场启用新的矩阵合成来修复破裂AF的潜在技术。以前的研究表明,当用合适的生长因子处理时,人脂肪干细胞(HASCs)能够分化为AF表型。由于其短暂的半衰期,高成本和低效率,临床应用中的生长因素使用涉及使用。该研究项目的主要目的是使用HASC和血清无软骨培养基在体外再生AF组织,而不会补充生长因子。通过使用微培养技术诱导HASC的分化。使用在商业AF生长培养基中培养的人环纤维纤维(HAFC)作为阳性对照。哈姆斯和HAFCs的AF表型对培养的14和21天进行了评估。硫酸化糖胺聚糖(GAG)含量的定量表明,在软骨生培养基中培养的HAFS表达了与HAFCS相似的硫酸化堵塞。 QRT-PCR通过AF表型证实了分化的HASCS的相似性。在HAFC和分化的HAFCs中表达了AF表型(蛋白,胶原蛋白I和甘糖蛋白-3)的几个标记。这是第一项研究表明HASC可以使用无血清软骨型培养基对AF表型分化而没有生长因子。在下一步骤中,由可生物降解的聚合物制造的支架将与ASCS组合使用以找到最佳构造以修复AF缺陷。

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