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

被引:11
作者
Danalache, Marina [1 ]
Kliesch, Sophie-Maria [2 ]
Munz, Marita [3 ]
Naros, Andreas [3 ]
Reinert, Siegmar [3 ]
Alexander, Dorothea [3 ]
机构
[1] Univ Hosp, Dept Orthoped Surg, D-72076 Tubingen, Germany
[2] Qual Anal GmbH, D-72622 Nurtingen, Germany
[3] Univ Hosp, Dept Oral & Maxillofacial Surg, D-72076 Tubingen, Germany
关键词
bone mineral formation; fetal calf serum; human platelet lysate; osteoprogenitor jaw periosteal cells; mechanical properties; atomic force microscopy; Raman spectroscopy; MESENCHYMAL STEM-CELLS; HUMAN PLATELET LYSATE; FETAL BOVINE SERUM; RAMAN-SPECTROSCOPY; EXTRACELLULAR-MATRIX; OSTEOGENIC DIFFERENTIATION; SUBSTRATE STIFFNESS; GROWTH-FACTORS; TGF-BETA; EXPANSION;
D O I
10.3390/ijms20174193
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
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.
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页数:17
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