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生物活性玻璃诱导的成骨细胞分化:一项非侵入性光谱研究。

Bioactive glass-induced osteoblast differentiation: a noninvasive spectroscopic study.

作者信息

Jell G, Notingher I, Tsigkou O, Notingher P, Polak J M, Hench L L, Stevens M M

机构信息

Department of Materials, Imperial College London, London, SW7 2AZ, United Kingdom.

出版信息

J Biomed Mater Res A. 2008 Jul;86(1):31-40. doi: 10.1002/jbm.a.31542.

Abstract

Here, we report on a rapid, noninvasive biophotonics system using Raman spectroscopy to detect real-time biochemical changes in foetal osteoblasts (FOBs) following exposure to 45S5 Bioglass (BG)-conditioned media. Bio-Raman spectroscopy, combined with multivariate statistical analysis techniques (principal component analysis and least squares analysis), was able to noninvasively identify biochemical differences in FOBs cultured for different time periods and between FOBs exposed/or not to BG-conditioned media. Gene and protein expression studies were also performed for known markers of osteoblastic differentiation, namely, alkaline phosphatase, bone sialoprotein, and collagen type I. Quantitative RT-PCR confirmed upregulation of genes associated with osteoblast differentiation after exposure to BG-conditioned media. These results suggest that Raman spectroscopy can noninvasively detect biochemical changes in FOBs associated with differentiation. This technique could have important applications in the field of regenerative medicine by enabling rapid characterization of cell or organoid behavior on novel bioactive scaffolds without damage to either cell or biomaterial.

摘要

在此,我们报告了一种快速、无创的生物光子学系统,该系统使用拉曼光谱来检测胎儿成骨细胞(FOB)在暴露于45S5生物玻璃(BG)条件培养基后实时的生化变化。生物拉曼光谱结合多变量统计分析技术(主成分分析和最小二乘法分析),能够无创地识别在不同时间段培养的FOB以及暴露于/未暴露于BG条件培养基的FOB之间的生化差异。还对成骨细胞分化的已知标志物,即碱性磷酸酶、骨涎蛋白和I型胶原蛋白进行了基因和蛋白质表达研究。定量逆转录聚合酶链反应(qRT-PCR)证实,暴露于BG条件培养基后,与成骨细胞分化相关的基因上调。这些结果表明,拉曼光谱可以无创地检测与分化相关的FOB中的生化变化。通过能够在不损害细胞或生物材料的情况下快速表征新型生物活性支架上的细胞或类器官行为,该技术在再生医学领域可能具有重要应用。

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