Dadras Mehran, Marcus Katrin, Wagner Johannes Maximilian, Wallner Christoph, Becerikli Mustafa, Jaurich Henriette, Dittfeld Stephanie, Lehnhardt Marcus, Serschnitzki Bettina, Guntermann Annika, Schilde Lukas, Behr Björn, May Caroline
BG University Hospital Bergmannsheil, Department of Plastic Surgery, Bochum, Germany.
Medizinisches Proteom-Center, Ruhr-University Bochum, Bochum, Germany.
Data Brief. 2019 Nov 5;27:104748. doi: 10.1016/j.dib.2019.104748. eCollection 2019 Dec.
This article describes a mass spectrometry data set generated from osteogenic differentiated bone marrow stromal cells (BMSCs) and adipose tissue derived stromal cells (ASCs) of a 24-year old healthy donor. Before osteogenic differentiation and performing mass spectrometric measurements cells have been characterized as mesenchymal stromal cells via FACS-analysis positive for CD90 and CD105 and negative for CD14, CD34, CD45 and CD11b and tri-lineage differentiation. After osteogenic differentiation, both cell types were homogenized and then fractionated by SDS gel electrophoresis, resulting in 12 fractions. The proteins underwent an in-gel digestion, spiked with iRT peptides and analysed by nanoHPLC-ESI-MS/MS, resulting in 24 data files. The data files generated from the described workflow are hosted in the public repository ProteomeXchange with identifier PXD015026. The presented data set can be used as a spectral library for analysis of key proteins in the context of osteogenic differentiation of mesenchymal stromal cells for regenerative applications. Moreover, these data can be used to perform comparative proteomic analysis of different mesenchymal stromal cells or stem cells upon osteogenic differentiation. In addition, these data can also be used to determine the optimal settings for measuring proteins and peptides of interest.
本文描述了一个质谱数据集,该数据集来自一名24岁健康供体的成骨分化骨髓基质细胞(BMSCs)和脂肪组织来源的基质细胞(ASCs)。在进行成骨分化和质谱测量之前,通过FACS分析将细胞鉴定为间充质基质细胞,其CD90和CD105呈阳性,CD14、CD34、CD45和CD11b呈阴性,并具有三系分化能力。成骨分化后,将两种细胞类型匀浆,然后通过SDS凝胶电泳进行分级分离,得到12个级分。对蛋白质进行胶内消化,加入iRT肽,并用nanoHPLC-ESI-MS/MS进行分析,得到24个数据文件。从所述工作流程生成的数据文件存放在公共存储库ProteomeXchange中,标识符为PXD015026。所呈现的数据集可作为光谱库,用于分析间充质基质细胞成骨分化过程中的关键蛋白质,以用于再生应用。此外,这些数据可用于对不同间充质基质细胞或干细胞在成骨分化后的蛋白质组进行比较分析。此外,这些数据还可用于确定测量感兴趣的蛋白质和肽的最佳设置。