Zhang Jianfeng, Zhang Qi, Chen Jiaxin, Ni Jinhu, Zhang Zeng, Wang Gangliang, Song Liyang, Fan Shunwu, Chen Pengfei, Lin Xianfeng
Department of Orthopaedic Surgery, Sir Run Run Shaw Hospital, Medical College of Zhejiang University, 3 East Qing Chun Road, Hangzhou, Zhejiang Province 310016, P.R. China.
ACS Biomater Sci Eng. 2017 Dec 11;3(12):3503-3514. doi: 10.1021/acsbiomaterials.7b00548. Epub 2017 Oct 27.
The periosteum plays a key role in bone regeneration and an artificial bionic material is urgently required. The periostea on the tibia and skull differ with respect to the types of cells, microstructure, and components, leading to different biological functions and biomechanical properties. We aimed to prepare decellularized periosteum scaffolds derived from different origins and evaluate their angiogenic and osteogenic activities. Histological assessment of α-smooth muscle actin, bone morphogenetic protein-2, and alkaline phosphatase in tibial and calvarial periosteum tissues provided preliminary information on their differing angiogenic and osteogenic properties. We developed decellularization protocols to completely remove the periosteum cellular components and for good maintenance of the hierarchical multilayer structures and components of the extracellular matrix (ECM) with no cytotoxicity. Moreover, using a chicken egg chorioallantoic membrane assay and a nude mouse implantation model, we found that tibia-derived periosteum ECM had superior osteogenic activity and calvarium-derived ECM had good angiogenic activity. The preliminary mechanisms of differing activities were then evaluated by osteogenesis- and angiogenesis-related gene expression in human umbilical vein endothelial cell- and MC-3T3 cell-seeded ECM scaffolds. Thus, this study provides periosteum biomaterials that are derived from specific tissues and have different functional properties and structures, for use in bone regeneration.
骨膜在骨再生中起关键作用,因此迫切需要一种人工仿生材料。胫骨和颅骨的骨膜在细胞类型、微观结构和成分方面存在差异,导致其生物学功能和生物力学特性不同。我们旨在制备源自不同来源的脱细胞骨膜支架,并评估其血管生成和成骨活性。对胫骨和颅骨骨膜组织中的α-平滑肌肌动蛋白、骨形态发生蛋白-2和碱性磷酸酶进行组织学评估,为它们不同的血管生成和成骨特性提供了初步信息。我们开发了脱细胞方案,以完全去除骨膜细胞成分,并良好地维持细胞外基质(ECM)的分层多层结构和成分,且无细胞毒性。此外,通过鸡胚绒毛尿囊膜试验和裸鼠植入模型,我们发现源自胫骨的骨膜ECM具有优异的成骨活性,而源自颅骨的ECM具有良好的血管生成活性。然后,通过在接种人脐静脉内皮细胞和MC-3T3细胞的ECM支架中与成骨和血管生成相关的基因表达,评估了不同活性的初步机制。因此,本研究提供了源自特定组织、具有不同功能特性和结构的骨膜生物材料,用于骨再生。