Kobayashi Naoki, Nishi Tsuyoshi
Department of Biochemistry, Faculty of Pharmaceutical Sciences, Setsunan University, Hirakata, Osaka, 573-0101, Japan.
Department of Biomolecular Science and Regulation, Institute of Scientific and Industrial Research, Osaka University, Ibaraki, Osaka, 567-0047, Japan.
Methods Mol Biol. 2018;1697:73-82. doi: 10.1007/7651_2017_25.
Sphingosine-1-phosphate (S1P) is an intercellular signaling molecule that is present in the plasma and plays an important role in recruiting lymphocytes from the thymus and secondary lymphoid organs. Erythrocytes are the most abundant cells in the blood and substantially contribute to the S1P supply in the plasma by releasing intracellularly synthesized S1P via an S1P transporter. Thus, the S1P transporter in erythrocytes is a potential target for immuno-suppressing drugs.In this chapter, we describe a rapid method for measuring the activity of the erythrocyte S1P transporter by using the fluorescent S1P analog, 7-nitro-2-1,3-benzoxadiazol-4-yl (NBD)-labeled S1P. This method does not require chromatography performed with high-performance liquid chromatography, liquid chromatography-tandem mass spectrometry, or thin-layer chromatography methods. Furthermore, S1P transporter activity can be detected by measuring the increase in fluorescence intensity in the extracellular buffer without performing lipid extraction.
鞘氨醇-1-磷酸(S1P)是一种细胞间信号分子,存在于血浆中,在从胸腺和二级淋巴器官募集淋巴细胞方面发挥重要作用。红细胞是血液中最丰富的细胞,通过经由S1P转运蛋白释放细胞内合成的S1P,对血浆中的S1P供应有很大贡献。因此,红细胞中的S1P转运蛋白是免疫抑制药物的潜在靶点。在本章中,我们描述了一种通过使用荧光S1P类似物7-硝基-2-1,3-苯并恶二唑-4-基(NBD)标记的S1P来测量红细胞S1P转运蛋白活性的快速方法。该方法不需要使用高效液相色谱、液相色谱-串联质谱或薄层色谱法进行色谱分析。此外,无需进行脂质提取,通过测量细胞外缓冲液中荧光强度的增加即可检测S1P转运蛋白活性。