骨结合蛋白
间充质干细胞
骨桥蛋白
碱性磷酸酶
Von Kossa染色
骨钙素
运行x2
化学
纳米晶材料
结晶度
细胞生物学
分子生物学
生物化学
免疫学
生物
结晶学
酶
作者
Saeed Hesaraki,Hamid Nazarian,Milad Pourbaghi‐Masouleh,Shokoufeh Borhan
摘要
Abstract Hydroxyapatite with different characteristics in terms of morphology and chemistry were prepared via conventional sintering and low temperature biomimetic mineralization methods. The biomineralization route introduced nanocrystalline carbonate‐substituted hydroxyapatite ( n ‐CHA) with needle‐like crystals ranging 20–30 nm whereas sintered HA (S‐HA) comprised of polygonal grains ranging 2–5 μm. The response of fibroblastic cells was investigated using the extract of the samples whereas Wistar rat‐derived mesenchymal stem cells (MSCs) were evaluated on top of each sample while maintaining in an osteogenic‐free medium. The proliferation, activity, and morphology of adherent MSCs were determined at different culturing periods. The osteogenic differentiation of MSCs was also assayed by determining expression of runx2, osteonectin, osteopontin, and osteocalcin genes using real time‐PCR analysis. The fibroblastic cells exhibited better proliferation rate at the presence of n ‐CHA compared to S‐HA. Furthermore, the MSCs attached and spread well on both n ‐CHA and S‐HA with better proliferation rate and alkaline phosphatase activity on n ‐CHA. Interestingly, the osteogenic differentiation of MSCs on n ‐CHA was confirmed by the expression of bone specific proteins whereas poor expression of these proteins was detected for the cells on S‐HA. The results showed that the role of morphology, crystallinity, and chemistry of hydroxyapatite is crucial for osteogenesis differentiation of MSCs. The results predict osteoinductivity of n ‐CHA, because MSCs differentiation occurred at the absence of osteogenic medium. However, in vivo data are also required to support this suggestion. © 2013 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 102B: 108–118, 2014.
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