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不同培养条件下颌骨骨膜细胞形成的矿物质质量分析。

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

机构信息

Department of Orthopedic Surgery, University Hospital, 72076 Tübingen, Germany.

Quality Analysis GmbH, 72622 Nürtingen, Germany.

出版信息

Int J Mol Sci. 2019 Aug 27;20(17):4193. doi: 10.3390/ijms20174193.

Abstract

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 ( = 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 ( < 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 ( < 0.001). Additionally, significantly higher levels ( < 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 ( < 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 ( < 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.

摘要

先前,我们发现胎牛血清(FCS)中的矿化程度高于无血清培养的颌骨骨膜来源的成骨祖细胞(JPC)。通过拉曼光谱,我们在无血清培养基条件下检测到更早形成的、质量更高的矿化细胞外基质(ECM)。然而,矿化潜力仍然较低。在本研究中,我们旨在研究 JPC 形成的 ECM 和矿物质在人血小板裂解液(hPL)和 FCS 补充条件下的生物化学成分和随后的生物力学特性。JPC 从(= 4 个供体)分离出来并在 FCS 条件下扩增,在第 5 代时在 FCS 和 hPL 培养基补充条件下进行成骨诱导。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。原子力显微镜(AFM)用于评估生物力学特性。拉曼光谱测量结果表明,与 FCS 培养相比,在 hPL 培养的成骨诱导 JPC 中,磷酸盐与蛋白质的比值显著更高(<0.001),并且碳酸盐与磷酸盐的比值呈趋势性降低。此外,在 hPL 培养的细胞中检测到更高的晶体尺寸。就 ECM 而言,在 hPL 培养的 JPC 单层中,前体蛋白脯氨酸与羟脯氨酸的比值明显更高(<0.001)。此外,计算出的胶原蛋白交联水平也明显更高(<0.001),表明 hPL 培养的 JPC 中胶原蛋白成熟程度更高。通过原子力显微镜观察到,在 FCS 培养的 JPC 单层中,ECM 硬度显著增加(<0.001)。而在 JPC 形成的沉淀物/矿物质中则观察到相反的效果。在 hPL 补充下,与 FCS 相比,JPC 形成的矿物质的硬度明显更高(<0.001)。本研究表明,hPL 培养 JPC 可形成生化组成和机械性能更优的无机材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90da/6747376/700a75a43717/ijms-20-04193-g001.jpg

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