首页> 外文期刊>Journal of tissue engineering and regenerative medicine >Remodelling of human bone on the chorioallantoic membrane of the chicken egg: De novo De novo bone formation and resorption
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Remodelling of human bone on the chorioallantoic membrane of the chicken egg: De novo De novo bone formation and resorption

机译:人骨对鸡蛋绒毛炎膜的重塑:De Novo De Novo骨形成和吸收

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Abstract Traditionally used as an angiogenic assay, the chorioallantoic membrane (CAM) assay of the chick embryo offers significant potential as an in vivo model for xenograft organ culture. Viable human bone can be cultivated on the CAM and increases in bone volume are evident; however, it remains unclear by what mechanism this change occurs and whether this reflects the physiological process of bone remodelling. In this study we tested the hypothesis that CAM‐induced bone remodelling is a consequence of host and graft mediated processes. Bone cylinders harvested from femoral heads post surgery were placed on the CAM of green fluorescent protein (GFP)‐chick embryos for 9?days, followed by micro computed tomography (μCT) and histological analysis. Three‐dimensional registration of consecutive μCT‐scans showed newly mineralised tissue in CAM‐implanted bone cylinders, as well as new osteoid deposition histologically. Immunohistochemistry demonstrated the presence of bone resorption and formation markers (Cathepsin K, SOX9 and RUNX2) co‐localising with GFP staining, expressed by avian cells only. To investigate the role of the human cells in the process of bone formation, decellularised bone cylinders were implanted on the CAM and comparable increases in bone volume were observed, indicating that avian cells were responsible for the bone mineralisation process. Finally, CAM‐implantation of acellular collagen sponges, containing bone morphogenetic protein 2, resulted in the deposition of extracellular matrix and tissue mineralisation. These studies indicate that the CAM can respond to osteogenic stimuli and support formation or resorption of implanted human bone, providing a humanised CAM model for regenerative medicine research and a novel short‐term in vivo model for tissue engineering and biomaterial testing.
机译:摘要传统上用作血管生成测定,小鸡胚胎的胆管囊膜(CAM)测定作为异种移植器官文化的体内模型提供了显着的潜力。可以在凸轮上培养可行的人体骨,骨骼体积增加明显;然而,通过这种变化发生的机制以及这是否反映了骨重塑的生理过程,仍然不清楚。在这项研究中,我们测试了凸轮诱导的骨重塑是宿主和移植介导方法的假设。从股骨头手术中收获的骨缸放在绿色荧光蛋白(GFP)的凸轮上,为9?天,其次是微计算机断层扫描(μct)和组织学分析。连续μCT-扫描的三维登记在凸轮植入的骨筒中显示出新的矿化组织,以及组织学上的新骨质沉积。免疫组织化学证明存在骨吸收和形成标记(组织蛋白酶K,SOX9和RUNX2),其与GFP染色仅由GFP染色,仅由禽细胞表达。为了探讨人体细胞在骨形成过程中的作用,植入凸起的骨筒植入凸轮,观察到骨体积的相当增加,表明禽细胞负责骨矿化过程。最后,含有骨形态发生蛋白2的细胞胶原海绵的凸轮植入导致细胞外基质和组织矿化的沉积。这些研究表明,凸轮可以应对植入溶的刺激和支持形成或植入的人骨的复制,为组织工程和生物材料试验提供了用于再生医学研究的人性化凸轮模型和一种新的短期模型。

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