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Measurement of the Spatial Distribution of S1P in Small Quantities of Tissues: Development and Application of a Highly Sensitive LC-MS/MS Method Combined with Laser Microdissection

机译:少量组织中S1P空间分布的测量:结合激光显微切割的高灵敏度LC-MS / MS方法的开发和应用

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摘要

Sphingosine-1-phosphate (S1P) acts as an extracellular signaling molecule with diverse biological functions. Tissues appear to have an S1P gradient, which is functionally relevant in the biological significance of S1P, although its existence has not been measured directly. Here, we report a highly sensitive method to determine the distribution of S1P, using a column-switching LC-MS/MS system combined with laser microdissection (LMD). Column switching using narrow core Capcell Pak C18 analytical and trap columns with 0.3 mm inner diameter improved the performance of the LC-MS/MS system. The calibration curve of S1P showed good linearity (r>0.999) over the range of 0.05–10 nM (1–200 fmol/injection). The accuracy of the method was confirmed by measuring S1P-spiked laser microdissected mice tissue sections. To evaluate our S1P analytical method, we quantified S1P extracted from micro-dissected mouse brain and spleen. These results show that this method can measure low S1P concentrations and determine S1P distribution in tissue microenvironments.
机译:鞘氨醇-1-磷酸酯(S1P)是具有多种生物学功能的细胞外信号分子。组织似乎具有S1P梯度,在功能上与S1P的生物学意义相关,尽管尚未直接测量其存在。在这里,我们报告了一种高灵敏度的方法来确定S1P的分布,它使用了柱切换LC-MS / MS系统与激光显微切割(LMD)的组合。使用内径为0.3mm的窄芯Capcell Pak C18分析和捕集柱进行色谱柱切换,可改善LC-MS / MS系统的性能。 S1P的校准曲线在0.05–10 nM(1–200 fmol /进样)范围内显示出良好的线性(r> 0.999)。该方法的准确性通过测量S1P掺入的激光显微切割的小鼠组织切片来证实。为了评估我们的S1P分析方法,我们量化了从显微解剖的小鼠大脑和脾脏中提取的S1P。这些结果表明,该方法可测量低S1P浓度并确定S1P在组织微环境中的分布。

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