State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050, People's Republic of China.
Biomaterials. 2012 Mar;33(7):2076-85. doi: 10.1016/j.biomaterials.2011.11.042. Epub 2011 Dec 15.
Low oxygen pressure (hypoxia) plays an important role in stimulating angiogenesis; there are, however, few studies to prepare hypoxia-mimicking tissue engineering scaffolds. Mesoporous bioactive glass (MBG) has been developed as scaffolds with excellent osteogenic properties for bone regeneration. Ionic cobalt (Co) is established as a chemical inducer of hypoxia-inducible factor (HIF)-1α, which induces hypoxia-like response. The aim of this study was to develop hypoxia-mimicking MBG scaffolds by incorporating ionic Co(2+) into MBG scaffolds and investigate if the addition of Co(2+) ions would induce a cellular hypoxic response in such a tissue engineering scaffold system. The composition, microstructure and mesopore properties (specific surface area, nano-pore volume and nano-pore distribution) of Co-containing MBG (Co-MBG) scaffolds were characterized and the cellular effects of Co on the proliferation, differentiation, vascular endothelial growth factor (VEGF) secretion, HIF-1α expression and bone-related gene expression of human bone marrow stromal cells (BMSCs) in MBG scaffolds were systematically investigated. The results showed that low amounts of Co (<5%) incorporated into MBG scaffolds had no significant cytotoxicity and that their incorporation significantly enhanced VEGF protein secretion, HIF-1α expression, and bone-related gene expression in BMSCs, and also that the Co-MBG scaffolds support BMSC attachment and proliferation. The scaffolds maintain a well-ordered mesopore channel structure and high specific surface area and have the capacity to efficiently deliver antibiotics drugs; in fact, the sustained released of ampicillin by Co-MBG scaffolds gives them excellent anti-bacterial properties. Our results indicate that incorporating cobalt ions into MBG scaffolds is a viable option for preparing hypoxia-mimicking tissue engineering scaffolds and significantly enhanced hypoxia function. The hypoxia-mimicking MBG scaffolds have great potential for bone tissue engineering applications by combining enhanced angiogenesis with already existing osteogenic properties.
低氧压力(缺氧)在刺激血管生成中起着重要作用;然而,很少有研究制备模拟缺氧的组织工程支架。介孔生物活性玻璃(MBG)已被开发为具有优异成骨性能的支架,用于骨再生。离子钴(Co)已被确立为缺氧诱导因子 1α(HIF-1α)的化学诱导剂,可诱导类似缺氧的反应。本研究旨在通过将离子 Co(2+)掺入 MBG 支架中来制备模拟缺氧的 MBG 支架,并研究 Co(2+)离子的添加是否会在这种组织工程支架系统中诱导细胞缺氧反应。对含 Co 的 MBG(Co-MBG)支架的组成、微观结构和介孔特性(比表面积、纳米孔体积和纳米孔分布)进行了表征,并系统研究了 Co 对 MBG 支架中骨髓基质细胞(BMSCs)增殖、分化、血管内皮生长因子(VEGF)分泌、HIF-1α表达和骨相关基因表达的细胞影响。结果表明,低浓度(<5%)的 Co 掺入 MBG 支架中没有明显的细胞毒性,并且 Co 的掺入显著增强了 BMSCs 中 VEGF 蛋白的分泌、HIF-1α的表达和骨相关基因的表达,同时 Co-MBG 支架支持 BMSC 的附着和增殖。支架保持有序的介孔通道结构和高比表面积,并具有高效输送抗生素药物的能力;事实上,Co-MBG 支架中氨苄西林的持续释放赋予了它们优异的抗菌性能。我们的结果表明,将钴离子掺入 MBG 支架中是制备模拟缺氧的组织工程支架的可行方法,并显著增强了缺氧功能。模拟缺氧的 MBG 支架通过结合增强的血管生成和现有的成骨特性,在骨组织工程应用中具有巨大的潜力。