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Influence of calcium and phosphorus release from bioactive glasses on viability and differentiation of dental pulp stem cells

机译:生物活性玻璃中钙磷释放对牙髓干细胞活力和分化的影响

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摘要

The release of ions that can significantly contribute toward cellular response is an important characteristic of bioactive glasses (BG). Here, ionic extracts of three different compositions of BG powders in 60 mol% SiO2, x mol% CaO (x = 28, 32 and 36), x mol% P2O5 (x = 12, 8 and 4) compositional system were utilized to study their effect on the viability, differentiation and mineralization of dental pulp stem cells (DPSCs) in vitro. ICP was applied to detect the exact ionic concentrations released from different composition of BG. DPSCs treated with conditioned media from the glass with 4 mol% P2O5 (BGCM1, media containing 44.01 ± 0.6 mg/L Si, 61.72 ± 0.1 mg/L Ca and 7.57 ± 0.01 mg/L P) were more metabolically active compared to conditioned media from the glass with 8 mol% P2O5 (BGCM2, media with 47.36 ± 0.7 mg/L Si, 57.4 ± 0.1 mg/L Ca and 14.54 ± 0.2 mg/L P), at all times tested, but in all cases the process was slower than the control. Cells exposed to media conditioned by the glass with 12 mol% P2O5 (BGCM3, 40.46 ± 0.5 mg/L Si, 61. 85 ± 0.3 mg/L Ca and 28.43 ± 0.3 mg/L P) responded differently, such that cells showed to be more metabolically active than control at day 3, but then similar to or lower than control at higher time points. Differentiation of DPSCs toward osteogenic lineage in the presence of BGCM was assessed by Alizarin red staining. Cells treated with high phosphate BGCM3 displayed a higher density of red mineralized nodules than cells treated with BGCM1 and BGCM2 after 21 days of culture in non-osteogenic medium. BGCM3 was therefore chosen for gene expression studies. Osteogenic differentiation of DPSCs in the presence and/or absence of BGCM3 or osteogenic supplements were studied by RT-PCR. Overall, the results demonstrated that, in the absence of osteogenic supplements, BGCM3 group showed a significantly higher mRNA expression levels for alkaline phosphatase at day 7, osteopontin and osteonectin at days 7 and 14, and a high level of collagen I at day 14, compared to negative control group (BM−). Overall, the results obtained from BGCM3 group are beneficial for the design and manufacture of scaffolds or particulates with tailored ion release for a range of bone repair applications.
机译:可以显着促进细胞反应的离子的释放是生物活性玻璃(BG)的重要特征。在此,利用三种不同成分的BG粉末的离子提取物在60 mol%SiO2,x mol%CaO(x = 28、32和36),x mol%P2O5(x = 12、8和4)组成体系中进行研究它们对牙髓干细胞(DPSCs)的活力,分化和矿化的影响。 ICP用于检测从不同BG成分释放的确切离子浓度。与含有4 mol%P2O5的玻璃制成的条件培养基(BGCM1,含有44.01±0.6 mg / L Si,61.72±0.1 mg / L Ca和7.57±0.01 mg / LP的培养基)相比,DPSC的代谢活性更高。在所有时间测试都使用含8 mol%P2O5的玻璃(BGCM2,含47.36±0.7 mg / L Si,57.4±0.1 mg / L Ca和14.54±0.2 mg / LP的介质),但在所有情况下,该过程都比控制。暴露于玻璃中含有12 mol%P2O5(BGCM3,40.46±0.5 mg / L Si,61。85±0.3 mg / L Ca和28.43±0.3 mg / LP)的培养基中的细胞反应不同,因此显示出在第3天,新陈代谢的活性高于对照,但在较高的时间点,则与对照相似或低于对照。通过茜素红染色评估在BGCM存在下DPSC向成骨谱系的分化。在非成骨培养基中培养21天后,用高磷酸盐BGCM3处理的细胞显示出比用BGCM1和BGCM2处理的细胞更高的红色矿化结核密度。因此,选择了BGCM3进行基因表达研究。通过RT-PCR研究了在存在和/或不存在BGCM3或成骨补充剂的情况下DPSC的成骨分化。总体而言,结果表明,在没有成骨补充剂的情况下,BGCM3组在第7天时碱性磷酸酶的mRNA表达水平明显升高,在第7天和第14天时骨桥蛋白和骨连接素的表达水平较高,在第14天时,胶原蛋白I的水平较高。与阴性对照组(BM-)相比。总体而言,从BGCM3组获得的结果对于设计和制造具有定制的离子释放能力的支架或颗粒非常有用,适用于一系列骨修复应用。

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