首页> 外文期刊>Acta biomaterialia >Characterization of zinc-releasing three-dimensional bioactive glass scaffolds and their effect on human adipose stem cell proliferation and osteogenic differentiation.
【24h】

Characterization of zinc-releasing three-dimensional bioactive glass scaffolds and their effect on human adipose stem cell proliferation and osteogenic differentiation.

机译:释放锌的三维生物活性玻璃支架的表征及其对人脂肪干细胞增殖和成骨分化的影响。

获取原文
获取原文并翻译 | 示例
           

摘要

While the addition of zinc ions to bioactive ceramics has been shown to enhance the proliferation and osteogenic differentiation of osteoblast-like cells, contradictory results have been found. Therefore, the effect of zinc-releasing ceramics on cell proliferation and differentiation into osteogenic lineages requires further clarification. The aim of this study was to evaluate the effects of zinc addition on the degradation profile of three-dimensional bioactive glass scaffold, and on the proliferation and osteogenesis of human adipose stem cells (hASCs) in these scaffolds. Bioactive glass scaffolds containing Na(2)O, K(2)O, MgO, CaO, B(2)O(3), TiO(2), P(2)O(5) and SiO(2) were prepared. The degradation was evaluated by weight loss measurement, scanning electron microscopy and elemental analysis. The degradation profile of bioactive glass was shown to slow down with the addition of zinc. Qualitative live/dead staining showed that zinc addition to bioactive glass inhibits cell spreading and proliferation of hASCs. However, zinc addition had no significant effect on DNA content, alkaline phosphatase activity and osteopontin concentration of hASCs when measured quantitatively. Our results suggest that the possible stimulatory effect of addition of zinc on hASC proliferation and osteogenesis was not detected because addition of zinc slowed down the degradation rate of the studied bioactive glass scaffolds.
机译:虽然已显示向生物活性陶瓷中添加锌离子可增强成骨细胞样细胞的增殖和成骨分化,但发现矛盾的结果。因此,需要进一步阐明锌释放陶瓷对细胞增殖和分化为成骨谱系的作用。这项研究的目的是评估锌添加对三维生物活性玻璃支架的降解特性以及人类脂肪干细胞(hASCs)在这些支架中的增殖和成骨的影响。制备包含Na(2)O,K(2)O,MgO,CaO,B(2)O(3),TiO(2),P(2)O(5)和SiO(2)的生物活性玻璃支架。通过重量损失测量,扫描电子显微镜和元素分析评估降解。结果表明,添加锌可降低生物活性玻璃的降解速度。定性活/死染色表明,向生物活性玻璃中添加锌可抑制hASCs的细胞扩散和增殖。然而,定量测定时,添加锌对hASCs的DNA含量,碱性磷酸酶活性和骨桥蛋白浓度没有显着影响。我们的结果表明,未发现添加锌对hASC增殖和成骨的可能的刺激作用,因为添加锌会减慢所研究的生物活性玻璃支架的降解速度。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号