Fan Zhihai, Liu Hongxiang, Shi Shilei, Ding Zhaozhao, Zhang Zhen, Lu Qiang, Kaplan David L
Department of Orthopedics, The Second Affiliated Hospital of Soochow University, Soochow University, Suzhou, 215000, PR China.
National Engineering Laboratory for Modern Silk & Collaborative Innovation Center of Suzhou Nano Science and Technology, Soochow University, Suzhou, 215123, PR China.
Mater Today Bio. 2022 May 13;15:100283. doi: 10.1016/j.mtbio.2022.100283. eCollection 2022 Jun.
Osteogenesis-angiogenesis coupling processes play a crucial role in bone regeneration. Here, electric field induced aligned nanofiber layers with tunable thickness were coated on the surface of pore walls inside the deferoxamine (DFO)-laden silk fibroin (SF) and hydroxyapatite (HA) composite scaffolds to regulate the release of DFO to control vascularization dynamically. Longer electric field treatments resulted in gradually thickening layers to reduce the release rate of DFO where the released amount of DFO decreased gradually from 84% to 63% after 28 days. Besides the osteogenic capacity of HA, the changeable release of DFO brought different angiogenic behaviors in bone regeneration process, which provided a desirable niche with osteogenic and angiogenic cues. Anisotropic cues were introduced to facilitate cell migration inside the scaffolds. Changeable cytokine secretion from endothelial cells cultured in the different scaffolds revealed the regulation of cell responses related to vascularization . Peak expression of angiogenic factors appeared at days 7, 21 and 35 for endothelial cells cultured in the scaffolds with different silk nanofier layers, suggesting the dynamical regulation of angiogenesis. Although all of the scaffolds had the same silk and HA composition, cell studies indicated different osteogenic capacities for the scaffolds, suggesting that the regulation of DFO release also influenced osteogenesis outcomes . , the best bone regeneration occurred in defects treated with the composite scaffolds that exhibited the best osteogenic capacity . Using a rat bone defect model, healing was achieved within 12 weeks, superior to those treated with previous SF-HA composite matrices. Controlling angiogenic properties of bone biomaterials dynamically is an effective strategy to improve bone regeneration capacity.
骨生成-血管生成耦合过程在骨再生中起着关键作用。在此,将电场诱导的具有可调厚度的取向纳米纤维层涂覆在负载去铁胺(DFO)的丝素蛋白(SF)和羟基磷灰石(HA)复合支架内孔壁表面,以调节DFO的释放,从而动态控制血管生成。较长时间的电场处理导致层逐渐增厚,以降低DFO的释放速率,28天后DFO的释放量从84%逐渐降至63%。除了HA的成骨能力外,DFO的可变释放使骨再生过程中出现不同的血管生成行为,这提供了一个具有成骨和血管生成信号的理想微环境。引入各向异性信号以促进细胞在支架内迁移。在不同支架中培养的内皮细胞分泌的可变细胞因子揭示了与血管生成相关的细胞反应的调节。在具有不同丝纳米纤维层的支架中培养的内皮细胞,血管生成因子的峰值表达分别出现在第7天、第21天和第35天,表明血管生成受到动态调节。尽管所有支架具有相同的丝和HA组成,但细胞研究表明这些支架具有不同的成骨能力,这表明DFO释放的调节也影响成骨结果。在具有最佳成骨能力的复合支架治疗的缺损中,实现了最佳的骨再生。使用大鼠骨缺损模型,在12周内实现了愈合,优于用先前的SF-HA复合基质治疗的情况。动态控制骨生物材料的血管生成特性是提高骨再生能力的有效策略。