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生物活性玻璃离子作为人脂肪干细胞成骨分化的强增强剂。

Bioactive glass ions as strong enhancers of osteogenic differentiation in human adipose stem cells.

机构信息

Adult Stem Cell Research Group, University of Tampere, Tampere, Finland; BioMediTech, University of Tampere and Tampere University of Technology, Tampere, Finland; Science Centre, Tampere University Hospital, Tampere, Finland.

Adult Stem Cell Research Group, University of Tampere, Tampere, Finland; BioMediTech, University of Tampere and Tampere University of Technology, Tampere, Finland; Science Centre, Tampere University Hospital, Tampere, Finland.

出版信息

Acta Biomater. 2015 Jul;21:190-203. doi: 10.1016/j.actbio.2015.04.017. Epub 2015 Apr 18.

Abstract

Bioactive glasses are known for their ability to induce osteogenic differentiation of stem cells. To elucidate the mechanism of the osteoinductivity in more detail, we studied whether ionic extracts prepared from a commercial glass S53P4 and from three experimental glasses (2-06, 1-06 and 3-06) are alone sufficient to induce osteogenic differentiation of human adipose stem cells. Cells were cultured using basic medium or osteogenic medium as extract basis. Our results indicate that cells stay viable in all the glass extracts for the whole culturing period, 14 days. At 14 days the mineralization in osteogenic medium extracts was excessive compared to the control. Parallel to the increased mineralization we observed a decrease in the cell amount. Raman and Laser Induced Breakdown Spectroscopy analyses confirmed that the mineral consisted of calcium phosphates. Consistently, the osteogenic medium extracts also increased osteocalcin production and collagen Type-I accumulation in the extracellular matrix at 13 days. Of the four osteogenic medium extracts, 2-06 and 3-06 induced the best responses of osteogenesis. However, regardless of the enhanced mineral formation, alkaline phosphatase activity was not promoted by the extracts. The osteogenic medium extracts could potentially provide a fast and effective way to differentiate human adipose stem cells in vitro.

摘要

生物活性玻璃以其诱导干细胞成骨分化的能力而闻名。为了更详细地阐明其成骨诱导机制,我们研究了从商业玻璃 S53P4 和三种实验玻璃(2-06、1-06 和 3-06)中制备的离子提取物是否足以单独诱导人脂肪干细胞的成骨分化。细胞使用基础培养基或成骨培养基作为提取物基础进行培养。我们的结果表明,细胞在整个培养期 14 天内都能在所有玻璃提取物中保持存活。在 14 天时,与对照相比,成骨培养基提取物中的矿化过度。与矿化增加平行的是细胞数量的减少。拉曼和激光诱导击穿光谱分析证实,矿物由磷酸钙组成。一致地,成骨培养基提取物还在 13 天增加了细胞外基质中骨钙素的产生和胶原蛋白 I 的积累。在四种成骨培养基提取物中,2-06 和 3-06 诱导了最好的成骨反应。然而,无论矿物形成增强如何,提取物都不能促进碱性磷酸酶的活性。成骨培养基提取物可能为体外人脂肪干细胞的快速有效分化提供了一种方法。

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