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Ex Vivo Bone Formation in Bovine Trabecular Bone Cultured in a Dynamic 3D Bioreactor Is Enhanced by Compressive Mechanical Strain

机译:动态3D生物反应器中培养的牛小梁骨中的体内骨骼形成通过压缩机械应变增强

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摘要

Our aim was to test cell and trabecular responses to mechanical loading in vitro in a tissue bone explant culture model. We used a new three-dimensional culture model, the ZetOS™ system, which provides the ability to exert cyclic compression on cancellous bone cylinders (bovine sternum) cultured in forced flow circumfusion chambers, and allows to assess mechanical parameters of the cultivated samples. We evaluated bone cellular parameters through osteocyte viability test, gene and protein expression, and histomorphometric bone formation rate, in nonloaded versus loaded samples. The microarchitecture of bone cores was appraised by in vivo micro-CT imaging. After 3 weeks, the samples receiving daily cyclic compression exhibited increased osteoblast differentiation and activity associated with thicker, more plate-like-shaped trabeculae and higher Young's modulus and ultimate force as compared to unloaded samples. Osteoclast activity was not affected by mechanical strain, although it was responsive to drug treatments (retinoic acid and bisphosphonate) during the first 2 weeks of culture. Thus, in the ZetOS apparatus, we reproduce in vitro the osteogenic effects of mechanical strain known in vivo, making this system a unique and an essential laboratory aid for ex vivo testing of lamellar bone remodeling.
机译:我们的目的是在组织骨外植体培养模型中测试细胞和小梁对体外机械负荷的反应。我们使用了一种新的三维培养模型ZetOS™系统,该模型可以对强制流回血室中培养的松质骨圆柱体(牛胸骨)施加周期性压缩,并可以评估培养样品的机械参数。我们通过骨细胞存活力测试,基因和蛋白质表达以及组织形态计量学的骨形成速率,在未加载与加载样品中评估了骨细胞参数。通过体内微CT成像评估骨核的微结构。 3周后,与未加载样品相比,接受每日循环压缩的样品显示出成骨细胞分化增强和活性增加,与较厚,更多的板状小梁以及更高的杨氏模量和极限力相关。破骨细胞活性不受机械应变的影响,尽管在培养的前2周中它对药物处理(视黄酸和双膦酸酯)有反应。因此,在ZetOS设备中,我们在体外复制了体内已知的机械应变的成骨作用,从而使该系统成为用于离体测试片状骨重塑的独特且必不可少的实验室辅助工具。

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  • 来源
    《Tissue Engineering Part A》 |2008年第1期|117-126|共10页
  • 作者单位

    INSERM U890, Laboratoire de Biologie du Tissu Osseux, IFR143, IFRESIS, Université Jean Monnet, St. Etienne, F-42023, France.|Present address: The Kidney Institute, University of Kansas Medical Center, Kansas City, Kansas.;

    INSERM U890, Laboratoire de Biologie du Tissu Osseux, IFR143, IFRESIS, Université Jean Monnet, St. Etienne, F-42023, France.;

    INSERM U890, Laboratoire de Biologie du Tissu Osseux, IFR143, IFRESIS, Université Jean Monnet, St. Etienne, F-42023, France.|Present address: The Kidney Institute, University of Kansas Medical Center, Kansas City, Kansas.;

    INSERM U890, Laboratoire de Biologie du Tissu Osseux, IFR143, IFRESIS, Université Jean Monnet, St. Etienne, F-42023, France.;

    INSERM U890, Laboratoire de Biologie du Tissu Osseux, IFR143, IFRESIS, Université Jean Monnet, St. Etienne, F-42023, France.;

    INSERM U890, Laboratoire de Biologie du Tissu Osseux, IFR143, IFRESIS, Université Jean Monnet, St. Etienne, F-42023, France.;

    Scottish Mechanotransduction Consortium, Medical School, University of Edinburgh, Edinburgh, United Kingdom.;

    Scottish Mechanotransduction Consortium, Medical School, University of Edinburgh, Edinburgh, United Kingdom.;

    Department of Experimental Orthopaedics and Biomechanics, Philipps University, Marburg, Germany.;

    INSERM U890, Laboratoire de Biologie du Tissu Osseux, IFR143, IFRESIS, Université Jean Monnet, St. Etienne, F-42023, France.;

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