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Osteoinduction and survival of osteoblasts and bone-marrow stromal cells in 3D biphasic calcium phosphate scaffolds under static and dynamic culture conditions

机译:静态和动态培养条件下3D双相磷酸钙支架中成骨细胞和骨髓基质细胞的成骨诱导和存活

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摘要

In many tissue engineering approaches, the basic difference between in vitro and in vivo conditions for cells within three-dimensional (3D) constructs is the nutrition flow dynamics. To achieve comparable results in vitro, bioreactors are advised for improved cell survival, as they are able to provide a controlled flow through the scaffold. We hypothesize that a bioreactor would enhance long-term differentiation conditions of osteogenic cells in 3D scaffolds. To achieve this either primary rat osteoblasts or bone marrow stromal cells (BMSC) were implanted on uniform-sized biphasic calcium phosphate (BCP) scaffolds produced by a 3D printing method. Three types of culture conditions were applied: static culture without osteoinduction (Group A); static culture with osteoinduction (Group B); dynamic culture with osteoinduction (Group C). After 3 and 6 weeks, the scaffolds were analysed by alkaline phosphatase (ALP), dsDNA amount, SEM, fluorescent labelled live-dead assay, and real-time RT-PCR in addition to weekly alamarBlue assays. With osteoinduction, increased ALP values and calcium deposition are observed; however, under static conditions, a significant decrease in the cell number on the biomaterial is observed. Interestingly, the bioreactor system not only reversed the decreased cell numbers but also increased their differentiation potential. We conclude from this study that a continuous flow bioreactor not only preserves the number of osteogenic cells but also keeps their differentiation ability in balance providing a suitable cell-seeded scaffold product for applications in regenerative medicine.
机译:在许多组织工程学方法中,三维(3D)构造中细胞的体外条件与体内条件之间的基本差异是营养流动动态。为了在体外获得可比的结果,建议生物反应器改善细胞存活率,因为它们能够提供通过支架的受控流。我们假设生物反应器将增强3D支架中成骨细胞的长期分化条件。为了实现这一目标,将原代大鼠成骨细胞或骨髓基质细胞(BMSC)植入通过3D打印方法生产的均一尺寸的双相磷酸钙(BCP)支架上。应用了三种类型的培养条件:无骨诱导的静态培养(A组);和带骨诱导的静态培养(B组);骨诱导动态培养(C组)。 3和6周后,除了每周进行alamarBlue分析外,还通过碱性磷酸酶(ALP),dsDNA量,SEM,荧光标记的活死分析和实时RT-PCR对支架进行分析。通过骨诱导,观察到ALP值增加和钙沉积。然而,在静态条件下,观察到生物材料上细胞数量的显着减少。有趣的是,生物反应器系统不仅逆转了减少的细胞数量,而且增加了其分化潜能。我们从这项研究中得出结论,连续流动生物反应器不仅保留了成骨细胞的数量,而且还保持了其分化能力的平衡,从而为再生医学中的应用提供了合适的细胞播种支架产品。

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