1 Department of Orthopedic Surgery, Mayo Clinic , Rochester, Minnesota.
2 Glycotherapeutics Group, Institute of Medical Biology , Agency for Science, Technology and Research (A*STAR), Singapore .
Tissue Eng Part C Methods. 2017 Nov;23(11):686-693. doi: 10.1089/ten.TEC.2017.0205. Epub 2017 Jul 3.
Animal models are vital tools for the preclinical development and testing of therapies aimed at providing solutions for several musculoskeletal disorders. For bone tissue engineering strategies addressing nonunion conditions, rodent models are particularly useful for studying bone healing in a controlled environment. The mouse calvarial defect model permits evaluation of drug, growth factor, or cell transplantation efficacy, together with offering the benefit of utilizing genetic models to study intramembranous bone formation within defect sites. In this study, we describe a detailed methodology for creating calvarial defects in mouse and present our results on bone morphogenetic protein-2-loaded fibrin scaffolds, thus advocating the utility of this functional orthotopic mouse model for the evaluation of therapeutic interventions (such as growth factors or cells) intended for successful bone regeneration therapies.
动物模型是针对几种肌肉骨骼疾病的治疗方法进行临床前开发和测试的重要工具。对于旨在解决骨不连的骨组织工程策略,啮齿动物模型特别有助于在受控环境中研究骨愈合。小鼠颅骨缺损模型允许评估药物、生长因子或细胞移植的疗效,同时还可以利用遗传模型来研究缺陷部位内的膜内骨形成。在这项研究中,我们描述了一种在小鼠中创建颅骨缺损的详细方法,并介绍了我们关于骨形态发生蛋白 2 负载纤维蛋白支架的结果,从而提倡使用这种功能性原位小鼠模型来评估旨在成功进行骨再生治疗的治疗干预(如生长因子或细胞)。