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A Bone-Implant Interaction Mouse Model for Evaluating Molecular Mechanism of Biomaterials/Bone Interaction

机译:用于评估生物材料/骨相互作用分子机制的骨-植入物相互作用小鼠模型

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The development of an optimal animal model that could provide fast assessments of the interaction between bone and orthopedic implants is essential for both preclinical and theoretical researches in the design of novel biomaterials. Compared with other animal models, mice have superiority in accessing the well-developed transgenic modification techniques (e.g., cell tracing, knockoff, knockin, and so on), which serve as powerful tools in studying molecular mechanisms. In this study, we introduced the establishment of a mouse model, which was specifically tailored for the assessment of bone-implant interaction in a load-bearing bone marrow microenvironment and could potentially allow the molecular mechanism study of biomaterials by using transgenic technologies. The detailed microsurgery procedures for developing a bone defect (Phi=0.8 mm) at the metaphysis region of the mouse femur were recorded. According to our results, the osteoconductive and osseointegrative properties of a well-studied 45S5 bioactive glass were confirmed by utilizing our mouse model, verifying the reliability of this model. The feasibility and reliability of the present model were further checked by using other materials as objects of study. Furthermore, our results indicated that this animal model provided a more homogeneous tissue-implant interacting surface than the rat at the early stage of implantation and this is quite meaningful for conducting quantitative analysis. The availability of transgenic techniques to mechanism study of biomaterials was further testified by establishing our model on Nestin-GFP transgenic mice. Intriguingly, the distribution of Nestin(+) cells was demonstrated to be recruited to the surface of 45S5 glass as early as 3 days postsurgery, indicating that Nestin(+) lineage stem cells may participate in the subsequent regeneration process. In summary, the bone-implant interaction mouse model could serve as a potential candidate to evaluate the early stage tissue response near the implant surface in a bone marrow microenvironment, and it also shows great potential in making transgenic animal resource applicable to biomaterial studies, so that the design of novel biomaterials could be better guided.
机译:对于新型生物材料设计中的临床前和理论研究而言,开发一种能够快速评估骨骼与整形外科植入物之间相互作用的最佳动物模型至关重要。与其他动物模型相比,小鼠在获得发达的转基因修饰技术(例如细胞追踪,敲除,敲入等)方面具有优势,它们是研究分子机制的有力工具。在这项研究中,我们介绍了一种小鼠模型的建立,该模型专门用于评估承重骨髓微环境中的骨-植入物相互作用,并有可能通过使用转基因技术进行生物材料的分子机理研究。记录了在小鼠股骨干meta端区域发展出骨缺损(Phi = 0.8 mm)的详细显微手术程序。根据我们的研究结果,利用我们的小鼠模型证实了经过充分研究的45S5生物活性玻璃的骨传导性和骨整合性,从而验证了该模型的可靠性。通过使用其他材料作为研究对象,进一步检验了该模型的可行性和可靠性。此外,我们的结果表明,该动物模型在植入早期提供了比大鼠更均匀的组织-植入物相互作用表面,这对于进行定量分析非常有意义。通过在Nestin-GFP转基因小鼠上建立我们的模型,进一步证明了转基因技术在生物材料机理研究中的可用性。有趣的是,证明Nestin(+)细胞的分布最早在手术后3天被募集到45S5玻璃的表面,这表明Nestin(+)谱系干细胞可能参与了随后的再生过程。综上所述,骨-植入物相互作用小鼠模型可以作为评估骨髓微环境中植入物表面附近早期组织反应的潜在候选者,并且在使转基因动物资源适用于生物材料研究方面也显示出巨大的潜力,因此可以更好地指导新型生物材料的设计。

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