Quantitation of cyclic nucleotides in mammalian cells and in human urine by high-performance liquid chromatography/mass spectrometry

Abstract

Background The cyclic nucleotides adenosine 3’,5’-cyclic monophosphate (cAMP) and guanosine 3’,5’-cyclic monophosphate (cGMP) are well-known second messengers. They play an important role in signal transduction. They control numerous functions ranging from ion channel opening to regulation of gene expression. In 1963, cAMP and cGMP were detected in rat urine. Indeed, this was the first proof of cGMP in biolocigal systems [1]. In 1984, Newton et al. demonstrated the possible presence of cytidine 3’,5’-cyclic monophosphate (cCMP) in various rat tissues [2] and, two years later, of uridine 3’,5’-cyclic monophosphate (cUMP) [3] by fast atom bombardment. Furthermore, cCMP was supposedly detected in urine of patients with acute leukemia [4,5] by radioimmuno assay. These findings point to a biological function of cCMP and cUMP. However, due to significant methodological problems, studies of the biological function of cCMP und cUMP were no longer continued. Recently, we have developed a method based on highperformance liquid chromatography-coupled mass spectrometry (HPLC-MS/MS), which allows the simultaneous determination of all cyclic nucleotides (cNMPs). Using this highly sensitive method we were able to detect and quantify cAMP, cGMP and cCMP as well as cUMP in various mammalian cell lines. We have optimized this method for the quantitation of cyclic nucleotides in complex biolocigal matrices, like urine and organs. Methods Nucleotide extraction of cells was performed by treating cells with a mixture of organic solvents and heating the samples at 98°C. After centrifugation the supernatant fluid was evaporated under a nitrogen stream and the residual pellet was resuspended in water. Detection and quantitation of cNMPs was achieved by an analytical method based on HPLC-MS/MS. To avoid serious matrix effects due to the complex urine composition we enzymatically synthesized CNlabeled internal standards for each cyclic nucleotide. Urine sample preparation was achieved by treating urine with acetonitrile containing those standards. The readout was performed as described above. The cCMP concentration was normalized to mmol creatinine. Creatinine concentration in urine was determined by gas chromatography -MS.