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通过丝裂原活化蛋白激酶信号通路开发一种用于大骨缺损再生的锶释放氧化石墨烯/胶原蛋白基有机-无机纳米生物复合材料。

Developing a Strontium-Releasing Graphene Oxide-/Collagen-Based Organic-Inorganic Nanobiocomposite for Large Bone Defect Regeneration via MAPK Signaling Pathway.

作者信息

Chen Yahong, Zheng Zhiwei, Zhou Renpeng, Zhang Huizhong, Chen Chuhsin, Xiong Zhezhen, Liu Kai, Wang Xiansong

机构信息

Department of Plastic and Reconstructive Surgery, Shanghai Ninth People's Hospital , Shanghai Jiao Tong University School of Medicine , 639 Zhizaoju Road , Shanghai 200011 , P. R. China.

Shanghai Key Laboratory of Tissue Engineering, Shanghai Ninth People's Hospital, National Tissue Engineering Center of China , Shanghai Jiao Tong University School of Medicine , Shanghai 200011 , P. R. China.

出版信息

ACS Appl Mater Interfaces. 2019 May 1;11(17):15986-15997. doi: 10.1021/acsami.8b22606. Epub 2019 Apr 16.

Abstract

Significant efforts have been dedicated to fabricating favorable biomaterial-based bone substitutes for the repair of large bone defects. However, the development of bone biomaterials with suitable physiochemical and osteoinductive properties remains a challenge. Here, novel strontium-graphene oxide (Sr-GO) nanocomposites that allow long-term release of Sr ions are fabricated, which are used to reinforce collagen (Col) scaffolds through covalent cross-linking. The prepared Sr-GO-Col scaffold demonstrates significantly high water retention rates and excellent mechanical properties compared with unmodified Col scaffolds. The Sr-GO-modified Col scaffolds display a strong effect on adipose-derived stem cells by facilitating cell adhesion and osteogenic differentiation and by promoting the secretion of angiogenic factors to stimulate the in vitro tube formation of endothelial cells. Additionally, the secretion of angiogenic VEGF and osteogenic BMP-2 proteins is increased, which may be attributed to the synergistic effects of GO and Sr on the activation of the MAPK signaling pathway. The Sr-GO-Col constructs were then transplanted into rat critical-size calvarial bone defects, which showed the best bone regeneration and angiogenesis outcome at 12 weeks. Moreover, histological staining results show that the Sr-GO-Col group achieved complete defect bridging with the newly formed bone tissue and the residual Sr-GO nanoparticles are phagocytosed and degraded by multinucleated giant cells. These findings reveal that the incorporation of inorganic Sr-GO nanocomposites into biocompatible Col scaffolds is a viable strategy for fabricating favorable substitutes that enhance the regeneration of large bone defects.

摘要

人们已经付出了巨大努力来制造有利于修复大骨缺损的生物材料基骨替代物。然而,开发具有合适理化性质和骨诱导特性的骨生物材料仍然是一项挑战。在此,制备了能够长期释放锶离子的新型氧化锶-氧化石墨烯(Sr-GO)纳米复合材料,并通过共价交联用于增强胶原蛋白(Col)支架。与未改性的Col支架相比,制备的Sr-GO-Col支架显示出显著更高的保水率和优异的力学性能。Sr-GO改性的Col支架通过促进细胞黏附和成骨分化以及促进血管生成因子的分泌来刺激内皮细胞的体外管形成,从而对脂肪来源的干细胞产生强烈影响。此外,血管生成的VEGF和成骨的BMP-2蛋白的分泌增加,这可能归因于GO和Sr对MAPK信号通路激活的协同作用。然后将Sr-GO-Col构建体移植到大鼠临界尺寸的颅骨缺损处,在12周时显示出最佳的骨再生和血管生成结果。此外,组织学染色结果表明,Sr-GO-Col组实现了与新形成的骨组织的完全缺损桥接,残留的Sr-GO纳米颗粒被多核巨细胞吞噬和降解。这些发现表明,将无机Sr-GO纳米复合材料掺入生物相容性Col支架中是制造有利于增强大骨缺损再生的替代物的可行策略。

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