Rinne Sandra, Ramstad Kleiveland Charlotte, Kassem Moustapha, Lea Tor, Lundanes Elsa, Greibrokk Tyge
Institute of Immunology, Rikshospitalet-Radiumhospitalet Medical Centre, University of Oslo, N-0315 Oslo, Norway.
J Sep Sci. 2007 Aug;30(12):1860-9. doi: 10.1002/jssc.200700064.
An online 2-D strong cation exchange (SCX)-RP capillary liquid chromatographic (cLC) method with IT mass spectrometric (IT-MS/MS) detection for the simultaneous determination of prostaglandin (PG) A(1), PGD(2), PGE(1), PGE(2), PGF(2a), 6-keto-(6k)PGF(1a), and 15-Delta(12,14)-deoxy-PGJ(2) (15dPGJ(2)) in cell culture supernatants was developed and validated. Pretreatment of the cell culture supernatants included dilution and filtration, and the analysis time including all sample preparation steps was less than 50 min per sample. Peptides/proteins contained in the matrix were removed by the SCX column. LODs in the range of 0.4-2.2 ng/mL cell culture supernatant, recoveries higher than 80% and within- and between-day precisions of less than 30% RSDs were obtained. Human mesenchymal stem cells (hMSCs) were stimulated with cytokine-containing supernatants derived from activated T lymphocytes, and PG production was analyzed using the developed method. PGE(2 )was found in cultures from both untreated and stimulated hMSCs, while PGE(1) was present above the detection limit only in stimulated cells.
建立并验证了一种在线二维强阳离子交换(SCX)-反相毛细管液相色谱(cLC)法,结合离子阱质谱(IT-MS/MS)检测,用于同时测定细胞培养上清液中的前列腺素(PG)A1、PGD2、PGE1、PGE2、PGF2α、6-酮基-(6k)PGF1α和15-Δ(12,14)-脱氧-PGJ2(15dPGJ2)。细胞培养上清液的预处理包括稀释和过滤,每个样品包括所有样品制备步骤的分析时间少于50分钟。基质中含有的肽/蛋白质通过SCX柱去除。获得的细胞培养上清液检测限在0.4-2.2 ng/mL范围内,回收率高于80%,日内和日间精密度小于30%相对标准偏差。用人活化T淋巴细胞来源的含细胞因子上清液刺激人间充质干细胞(hMSCs),并使用所建立的方法分析PG的产生。在未处理和刺激的hMSCs培养物中均发现了PGE2,而PGE1仅在刺激细胞中高于检测限。