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Quality Analysis of Minerals Formed by Jaw Periosteal Cells under Different Culture Conditions

机译:不同培养条件下颌骨骨膜细胞形成矿物质的质量分析

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摘要

Previously, we detected a higher degree of mineralization in fetal calf serum (FCS) compared to serum-free cultured jaw periosteum derived osteoprogenitor cells (JPCs). By Raman spectroscopy, we detected an earlier formation of mineralized extracellular matrix (ECM) of higher quality under serum-free media conditions. However, mineralization potential remained too low. In the present study, we aimed to investigate the biochemical composition and subsequent biomechanical properties of the JPC-formed ECM and minerals under human platelet lysate (hPL) and FCS supplementation. JPCs were isolated (n = 4 donors) and expanded under FCS conditions and used in passage five for osteogenic induction under both, FCS and hPL media supplementation. Raman spectroscopy and Alizarin Red/von Kossa staining were employed for biochemical composition analyses and for visualization and quantification of mineralization. Osteocalcin gene expression was analyzed by quantitative PCR. Biomechanical properties were assessed by using atomic force microscopy (AFM). Raman spectroscopic measurements showed significantly higher (p < 0.001) phosphate to protein ratios and in the tendency, lower carbonate to phosphate ratios in osteogenically induced JPCs under hPL in comparison to FCS culturing. Furthermore, higher crystal sizes were detected under hPL culturing of the cells. With respect to the ECM, significantly higher ratios of the precursor protein proline to hydroxyproline were detected in hPL-cultured JPC monolayers (p < 0.001). Additionally, significantly higher levels (p < 0.001) of collagen cross-linking were calculated, indicating a higher degree of collagen maturation in hPL-cultured JPCs. By atomic force microscopy, a significant increase in ECM stiffness (p < 0.001) of FCS cultured JPC monolayers was observed. The reverse effect was measured for the JPC formed precipitates/minerals. Under hPL supplementation, JPCs formed minerals of significantly higher stiffness (p < 0.001) when compared to the FCS setting. This study demonstrates that hPL culturing of JPCs leads to the formation of an anorganic material of superior quality in terms of biochemical composition and mechanical properties.
机译:以前,与无血清培养的颌骨骨膜来源的骨祖细胞(JPC)相比,我们在胎牛血清(FCS)中检测到更高的矿化度。通过拉曼光谱法,我们检测到在无血清培养基条件下更高质量的矿化细胞外基质(ECM)的早期形成。但是,矿化潜力仍然太低。在本研究中,我们旨在研究在人血小板裂解物(hPL)和FCS补充下JPC形成的ECM和矿物质的生化组成和随后的生物力学特性。分离JPC(n = 4个供体)并在FCS条件下扩增,并在第五代中用于FCS和hPL培养基添加下的成骨诱导。拉曼光谱和茜素红/ von Kossa染色用于生化成分分析以及矿化的可视化和定量。通过定量PCR分析骨钙素基因表达。通过使用原子力显微镜(AFM)评估生物力学性能。与FCS培养相比,拉曼光谱测量显示,在hPL下,成骨诱导的JPC中磷酸盐/蛋白质比率明显更高(p <0.001),并且趋势是较低的碳酸盐/磷酸盐比率。此外,在细胞的hPL培养下检测到更高的晶体尺寸。关于ECM,在hPL培养的JPC单层中检测到前体蛋白脯氨酸与羟脯氨酸的比例明显更高(p <0.001)。此外,计算出的胶原蛋白交联水平明显更高(p <0.001),表明在hPL培养的JPC中胶原蛋白成熟度更高。通过原子力显微镜,观察到FCS培养的JPC单层的ECM刚度显着增加(p <0.001)。测量了JPC形成的沉淀物/矿物质的反向作用。在hPL补充下,与FCS设置相比,JPC形成的矿物质具有更高的硬度(p <0.001)。这项研究表明,在JPC的hPL培养中,就生化成分和机械性能而言,可以形成质量较高的无机材料。

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