| Literature DB >> 25838203 |
Heike Bähre1, Christina Hartwig2, Antje Munder3, Sabine Wolter4, Tane Stelzer5, Bastian Schirmer6, Ulrike Beckert7, Dara W Frank8, Burkhard Tümmler9, Volkhard Kaever10, Roland Seifert11.
Abstract
Mammalian cells contain the cyclic pyrimidine nucleotides cCMP and cUMP. It is unknown whether these tentative new second messenger molecules occur in vivo. We used high performance liquid chromatography quadrupole tandem mass spectrometry to quantitate nucleoside 3',5'-cyclic monophosphates. cCMP was detected in all organs studied, most notably pancreas, spleen and the female reproductive system. cUMP was not detected in organs, probably due to the intrinsically low sensitivity of mass spectrometry to detect this molecule and organ matrix effects. Intratracheal infection of mice with recombinant Pseudomonas aeruginosa harboring the nucleotidyl cyclase toxin ExoY massively increased cUMP in lung. The identity of cCMP and cUMP in organs was confirmed by high performance liquid chromatography quadrupole time of flight mass spectrometry. cUMP also appeared in serum, urine and faeces following infection. Taken together, this report unequivocally shows for the first time that cCMP and cUMP occur in vivo.Entities:
Keywords: Cyclic pyrimidine nucleotides; ExoY; Mass spectrometry; Pseudomonas aeruginosa
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Year: 2015 PMID: 25838203 PMCID: PMC4765920 DOI: 10.1016/j.bbrc.2015.03.115
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575