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Bioactive-glass ceramic with two crystalline phases (BioS-2P) for bone tissue engineering

机译:生物活性玻璃陶瓷,具有两个晶体阶段(BIOS-2P)用于骨组织工程

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We aimed to evaluate the in vitro osteogenic and osteoinductive potentials of BioS-2P and its ability to promote in vivo bone repair. To investigate osteogenic potential, UMR-106 osteoblastic cells were cultured on BioS-2P and Bioglass 45S5 discs in osteogenic medium. The osteoinductive potential was evaluated using mesenchymal stem cells (MSCs) cultured on BioS-2P, Bioglass 45S5 and polystyrene in non-osteogenic medium. Rat bone calvarial defects were implanted with BioS-2P scaffolds alone or seeded with MSCs. UMR-106 proliferation was similar for both materials, while alkaline phosphatase (ALP) activity and mineralization were higher for BioS-2P. Bone sialoprotein (BSP), RUNX2 and osteopontin (OPN) gene expression and BSP, OPN, ALP and RUNX2 protein expression were higher on BioS-2P. For MSCs, ALP activity was higher on Bioglass 45S5 than on BioS-2P and was lower on polystyrene. All genes were highly expressed on bioactive glasses compared to polystyrene. BioS-2P scaffolds promoted in vivo bone formation without differences in the morphometric parameters at 4, 8 and 12 weeks. After 8 weeks, the combination of BioS-2P with MSCs did not increase the quantity of new bone compared to the BioS-2P alone. To stimulate osteoblast activity, drive MSC differentiation and promote bone formation, BioS-2P is a good choice as a scaffold for bone tissue engineering.
机译:我们的目标是评估BIOS-2P的体外骨质和骨诱导潜力及其在体内骨修复中促进的能力。为了研究成骨潜力,在成骨培养基中培养UMR-106骨细胞和生物胶囊45S5个圆盘。使用在BIOS-2P,BioGlass 45S5和非骨质培养基中的聚苯乙烯上培养的间充质干细胞(MSC)评价骨诱导电位。将大鼠骨颅骨缺陷单独使用BIOS-2P支架或用MSC播种。两种材料的UMR-106增殖相似,而BIOS-2P的碱性磷酸酶(ALP)活性和矿化较高。 BIOS-2P对骨唾液蛋白(BSP),RUNX2和OSTEOPONTIN(OPN)基因表达和BSP,OPN,ALP和RUNX2蛋白表达较高。对于MSCs,BioGlass 45S5的AlP活性比BIOS-2P在BIOS-2P上较高,聚苯乙烯较低。与聚苯乙烯相比,所有基因在生物活性玻璃上高度表达。 BIOS-2P支架在体内骨形成中促进,在4,8和12周的情况下没有差异。 8周后,与单独的BIOS-2P相比,BIOS-2P与MSCs的组合没有增加新骨的量。为了刺激成骨细胞活性,驱动MSC分化和促进骨形成,BIOS-2P是骨组织工程支架的良好选择。

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