Developing a novel calcium magnesium silicate/graphene oxide incorporated silk fibroin porous scaffold with enhanced osteogenesis, angiogenesis and inhibited osteoclastogenesis

IF 3.9 3区 医学 Q2 ENGINEERING, BIOMEDICAL Biomedical materials Pub Date : 2022-04-08 DOI:10.1088/1748-605X/ac65cc
Tingting Wu, Binglin Li, Wen‐chan Huang, Xianli Zeng, Yiwan Shi, Zefeng Lin, Chengxiong Lin, Weikang Xu, Hong Xia, Tao Zhang
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引用次数: 2

Abstract

Recently, biofunctional ions (Mg2+, Si4+, etc) and graphene derivatives are proved to be promising in stimulating bone formation. In this study, a novel inorganic/organic composite porous scaffold based on silk fibroin (SF), graphene oxide (GO), and calcium magnesium silicate (CMS) was developed for bone repair. The porous scaffolds obtained by lyophilization showed a little difference in pore structure while GO and CMS displayed a good interaction with SF matrix. The addition of CMS with good mineralization potential and sustainedly release ability of biofunctional ions (Ca2+, Mg2+ and Si4+) increased the strength of SF scaffolds a little and facilitated the osteogenic differentiation of bone mesenchymal stem cells (BMSCs) by upregulating bone formation-related genes (ALP, COL1, OC and Runx2). The further incorporation of GO in SF scaffolds enhanced the compressive strength and water retention, and also remarkably promoted the osteogenic differentiation of BMSCs. Besides, the angiogenesis of human umbilical vein endothelial cells was significantly promoted by CMS/GO/SF scaffold extract through the upregulation of angiogenesis genes (eNOs and bFGF). Moreover, the osteoclastic formation ability of RAW264.7 cells was suppressed by the released ions from CMS/GO/SF scaffold through the down-regulation of CAK, MMP9 and TRAP. The promoted osteogenesis, angiogenesis and inhibited osteoclastogenesis functions of CMS/GO/SF composite scaffold may enable it as a novel therapy for bone repair and regeneration.
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新型硅酸钙镁/氧化石墨烯复合丝素多孔支架的研制具有增强成骨、血管生成和抑制破骨细胞生成的作用
近年来,生物功能离子(Mg2+, Si4+等)和石墨烯衍生物在刺激骨形成方面被证明是有前景的。本研究开发了一种基于丝素蛋白(SF)、氧化石墨烯(GO)和硅酸钙镁(CMS)的新型无机/有机复合多孔支架用于骨修复。冻干制备的多孔支架孔结构差异不大,而氧化石墨烯和CMS与SF基质的相互作用良好。具有良好矿化潜力和生物功能离子(Ca2+、Mg2+、Si4+)持续释放能力的CMS的加入,可使SF支架强度略有提高,并通过上调骨形成相关基因(ALP、COL1、OC、Runx2)促进骨间充质干细胞(BMSCs)的成骨分化。在SF支架中进一步掺入氧化石墨烯,可增强其抗压强度和保水能力,并显著促进骨髓间充质干细胞的成骨分化。此外,CMS/GO/SF支架提取物通过上调血管生成基因(eNOs和bFGF),显著促进人脐静脉内皮细胞的血管生成。此外,CMS/GO/SF支架释放的离子通过下调CAK、MMP9和TRAP抑制RAW264.7细胞的破骨形成能力。CMS/GO/SF复合支架具有促进骨生成、血管生成和抑制破骨细胞生成的功能,有望成为骨修复和再生的新疗法。
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来源期刊
Biomedical materials
Biomedical materials 工程技术-材料科学:生物材料
CiteScore
6.70
自引率
7.50%
发文量
294
审稿时长
3 months
期刊介绍: The goal of the journal is to publish original research findings and critical reviews that contribute to our knowledge about the composition, properties, and performance of materials for all applications relevant to human healthcare. Typical areas of interest include (but are not limited to): -Synthesis/characterization of biomedical materials- Nature-inspired synthesis/biomineralization of biomedical materials- In vitro/in vivo performance of biomedical materials- Biofabrication technologies/applications: 3D bioprinting, bioink development, bioassembly & biopatterning- Microfluidic systems (including disease models): fabrication, testing & translational applications- Tissue engineering/regenerative medicine- Interaction of molecules/cells with materials- Effects of biomaterials on stem cell behaviour- Growth factors/genes/cells incorporated into biomedical materials- Biophysical cues/biocompatibility pathways in biomedical materials performance- Clinical applications of biomedical materials for cell therapies in disease (cancer etc)- Nanomedicine, nanotoxicology and nanopathology- Pharmacokinetic considerations in drug delivery systems- Risks of contrast media in imaging systems- Biosafety aspects of gene delivery agents- Preclinical and clinical performance of implantable biomedical materials- Translational and regulatory matters
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