首页> 外文期刊>Tissue engineering, Part A >Effects of flow shear stress and mass transport on the construction of a large-scale tissue-engineered bone in a perfusion bioreactor
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Effects of flow shear stress and mass transport on the construction of a large-scale tissue-engineered bone in a perfusion bioreactor

机译:流动剪切应力和传质对灌注生物反应器中大规模组织工程化骨结构的影响

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摘要

Currently, a tissue-engineered bone is usually constructed using a perfusion bioreactor in vitro. In the perfusion culture, fluid flow can exert shear stress on the cells seeded on scaffold, improving the mass transport of the cells. This experiment studied the effects of flow shear stress and mass transport, respectively, on the construction of a large-scale tissue-engineered bone using the critical-sized β-tricalcium phosphate scaffold seeded with human bone marrow-derived mesenchymal stem cells (hBMSCs). This was done by changing flow rate and adding dextran into the media, thus changing the media's viscosity. The cells were seeded onto the scaffolds and were cultured in a perfusion bioreactor for up to 28 days with different fluid flow shear stress or different mass transport. When the mass transport was 3mL/min, the flow shear stress was, respectively, 0.005Pa (0.004-0.007Pa), 0.011Pa (0.009-0.013Pa), or 0.015Pa (0.013-0.018Pa) in different experiment group obtained by simulation and calculation using fluid dynamics. When the flow shear stress was 0.015Pa (0.013-0.018Pa), the mass transport was, respectively, 3, 6, or 9mL/min. After 28 days of culture, the construction of the tissue-engineered bone was assessed by osteogenic differentiation of hBMSCs and histological assay of the constructs. Extracellular matrix (ECM) was distributed throughout the entire scaffold and was mineralized in the perfusion culture after 28 days. Increasing flow shear stress accelerated the osteogenic differentiation of hBMSCs and improved the mineralization of ECM. However, increasing mass transport inhibited the formation of mineralized ECM. So, both flow shear stress and transport affected the construction of the large-scale tissue-engineered bone. Moreover, the large-scale tissue-engineered bone could be better produced in the perfusion bioreactor with 0.015Pa (0.013-0.018Pa) of fluid flow shear stress and 3mL/min of mass transport.
机译:当前,通常在体外使用灌注生物反应器来构建组织工程的骨。在灌注培养中,流体流动可对接种在支架上的细胞施加剪切应力,从而改善细胞的质量运输。该实验分别研究了临界剪切力的β-磷酸三钙支架植入人骨髓来源的间充质干细胞(hBMSCs)后,流动剪切应力和传质对构建大规模组织工程骨的影响。 。通过改变流速并将葡聚糖添加到介质中来完成,从而改变介质的粘度。将细胞播种到支架上,并在灌注生物反应器中以不同的流体流动剪切应力或不同的质量传递将其培养多达28天。当质量传递率为3mL / min时,通过以下方法获得的不同实验组的流动剪切应力分别为0.005Pa(0.004-0.007Pa),0.011Pa(0.009-0.013Pa)或0.015Pa(0.013-0.018Pa)。使用流体动力学进行模拟和计算。当流动剪切应力为0.015Pa(0.013-0.018Pa)时,质量传递分别为3、6或9mL / min。培养28天后,通过hBMSC的成骨分化和构建体的组织学分析来评估组织工程骨的构建。细胞外基质(ECM)分布在整个支架上,并在28天后在灌注培养物中矿化。流动切应力的增加加速了hBMSCs的成骨分化并改善了ECM的矿化作用。但是,增加的大众运输抑制了矿化的ECM的形成。因此,流动剪切应力和运输都影响了大型组织工程骨的构造。此外,在灌注生物反应器中,流体流动剪切应力为0.015Pa(0.013-0.018Pa)且质量传递率为3mL / min时,可以更好地生产大规模的组织工程骨。

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