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Research progress of micro/nano-bioactive glasses for bone and skin restoration

机译:微/纳米生物活性眼镜骨及皮肤恢复的研究进展

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The design and development of novel cell-mediated and gene-activated bioactive materials has become one of important research fields for tissue regeneration. In this study, the new type of bioactive materials: micro/nano-bioactive glasses (MNBG) were prepared using organic template synthesis combined with sol-gel technology. These new bioactive glasses possess high surface area, good cell compatibility, rapid bone bonding and the ability to stimulate new bone formation, enhance angiogenesis and wound healing. This research explained the detailed mechanisms on the cell-mediated and gene-activated function for osteogenesis, vascularization and wound healing related cells and genes. Firstly, when BG was co-cultured with osteoblasts, both BG contacted cells and surrounding cells experienced proliferation and differentiation, and the mRNA level of the bone healing maker such as osteocalcin, alkaline phosphatase and osteopontin were significantly up-regulated, which confirmed the gene-activated function of ionic dissolution products from bioactive glass on surrounding cells, and the gene activation effects can be directly affected by the ionic release quantity. Our study also showed that the p38 and ERK signaling pathways was activated in MSCs (mesenchymal stem cells), resulting in the directional differentiation into the osteoblasts. The released Si and Ca further promoted the expressions of the osteogenic genes and proteins, such as the Runx 2, ALP and OCN. Therefore, we concluded that the osteogenesis of BG was not only related to the fast biomineralization process, but also depended on the cell-mediated and gene-activated functions. Moreover, MNBG could activate the VEGF (vascular endothelial growth factor) signaling pathway and up-regulate the expressions of angiogenic genes and proteins such as the VEGF and VEGF receptor, resulting in the faster proliferation, migration and angiogensis of the endothelial cells. Futhermore, in vivo study showed that the TGF-β (Transforming growth factor-β) signaling pathway was also activated with the high level expression of α-SMA and collagen Ⅰ genes and proteins. Those co-effects resulted in the faster and better healing process of the normal and diabetic cutaneous wounds. In conclusion, Micro-/nano-bioactive glasses could be a promissing kind of biomaterials for hard tissue repair, and cutaneous wound healing.
机译:新型细胞介导和基因活化的生物活性材料的设计和开发已成为组织再生的重要研究领域之一。在该研究中,使用有机模板合成与溶胶 - 凝胶技术合并制备新型的生物活性材料:微/纳米生物活性玻璃(MNBG)。这些新的生物活性眼镜具有高表面积,良好的细胞相容性,快速骨键和刺激新骨形成的能力,增强血管生成和伤口愈合。该研究解释了对骨质发生,血管形成和伤口愈合相关细胞和基因的细胞介导和基因活化功能的详细机制。首先,当Bg与成骨细胞共培养时,BG接触细胞和周围细胞经历了增殖和分化,并且骨愈合制造商如骨钙素,碱性磷酸酶和骨桥蛋白的mRNA水平显着上调,证实了该基因离子溶解产物从生物活性玻璃对周围细胞的活化函数,并且基因活化效果可由离子释放量直接影响。我们的研究还表明,在MSCs(间充质干细胞)中激活P38和ERK信号通路,导致定向分化进入成骨细胞中。释放的Si和Ca进一步促进了成骨基因和蛋白质的表达,例如Runx 2,AlP和OCN。因此,我们得出结论,BG的骨发生不仅与快速生物矿化过程有关,而且还依赖于细胞介导和基因活化的功能。此外,MNBG可以激活VEGF(血管内皮生长因子)信号传导途径,上调血管生成基因和蛋白质如VEGF和VEGF受体的表达,导致内皮细胞的增殖,迁移和血管生成更快。在体内研究中,在体内研究表明,TGF-β(转化生长因子-β)信号传导途径也被α-SMA和胶原Ⅰ基因和蛋白质的高水平表达激活。这些协同效应导致正常和糖尿病皮肤伤口的速度更快,更好的愈合过程。总之,微/纳米生物活性玻璃可能是硬组织修复和皮肤伤口愈合的追踪生物材料。

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