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缺氧模拟介孔生物活性玻璃支架可控释放钴离子用于骨组织工程。

Hypoxia-mimicking mesoporous bioactive glass scaffolds with controllable cobalt ion release for bone tissue engineering.

机构信息

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.

出版信息

Biomaterials. 2012 Mar;33(7):2076-85. doi: 10.1016/j.biomaterials.2011.11.042. Epub 2011 Dec 15.

Abstract

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.

摘要

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。

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