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Simple evaluation method for osteoinductive capacity of cells or scaffolds using ceramic cubes

机译:使用陶瓷立方体的细胞或支架骨诱导能力的简单评估方法

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摘要

Mesenchymal stem cells are good candidates for the clinical application of bone repair because of their osteogenic differentiation potential, but in vivo osteoinduction potential should be verified for culture expanded cells before clinical application.This study analyzed in vivo bone formation by MSCs quantitatively after implantation of MSCs planted porous biphasic ceramic cubes into athymic mice. MSCs were divided into osteogenic differentiation-induced and normal groups and also tested in vitro to evaluate the degree of differentiation into osteoblast. The osteogenic induced group showed higher alkaline phosphatase and calcium level in vitro and corresponding higher level of bone formation in vivo compared to control group. Whereas there was no bone formation observed in fibroblast-implanted negative control group.In critical sized bone defect models, commonly used for evaluation of bone regeneration ability, it is difficult to distinguish between osteoinduction and osteoconduction, and quantitative analysis is not simple. However, this method for evaluating osteoinduction is both accurate and simple.In conclusion, the analysis of in vivo bone formation using porous ceramic cubes is a powerful and simple method for evaluating the osteoinduction ability of target cells and, furthermore, can be applied for evaluation of scaffolds for their osteoinductive properties.
机译:间充质干细胞具有成骨分化潜能,因此在骨修复的临床应用中是很好的候选者,但在临床应用之前应先对培养的扩增细胞进行体内骨诱导潜力的验证。这项研究定量分析了植入MSCs后MSCs的体内骨形成将多孔两相陶瓷立方体植入无胸腺小鼠中。 MSC分为成骨分化诱导组和正常组,并在体外进行测试以评估向成骨细胞的分化程度。与对照组相比,成骨诱导组在体外显示较高的碱性磷酸酶和钙水平,在体内相应地具有较高的骨形成水平。植入成纤维细胞的阴性对照组中没有观察到骨形成。在临界大小的骨缺损模型中(通常用于评估骨再生能力),很难区分骨诱导和骨传导,定量分析并不简单。然而,这种评估骨诱导能力的方法既准确又简单。总之,利用多孔陶瓷立方体分析体内骨形成是一种强大而简单的评估靶细胞骨诱导能力的方法,而且可以用于评估支架的骨诱导特性。

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