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Publication : Cyclic cytidine 3',5'-monophosphate (cCMP) signals via cGMP kinase I.

First Author  Desch M Year  2010
Journal  FEBS Lett Volume  584
Issue  18 Pages  3979-84
PubMed ID  20691687 Mgi Jnum  J:164397
Mgi Id  MGI:4833756 Doi  10.1016/j.febslet.2010.07.059
Citation  Desch M, et al. (2010) Cyclic cytidine 3',5'-monophosphate (cCMP) signals via cGMP kinase I. FEBS Lett 584(18):3979-84
abstractText  We analysed the function and intracellular signalling of the cyclic pyrimidinic nucleotide cCMP. The membrane-permeable cCMP analogue dibutyryl-cCMP mediated mouse aorta relaxation. cCMP activated purified cGMP-dependent protein kinase (cGK) Ialpha and Ibeta and stimulated cGK in aorta lysates. cCMP-induced relaxation was abolished in cGKI-knockout tissue. Additionally, deletion of inositol-trisphosphate receptor associated cGKI substrate (IRAG) suppressed cCMP-mediated relaxation. Signalling of cCMP via cGKI/IRAG appears to be of broader physiological importance because cCMP-mediated inhibition of platelet aggregation was absent in cGKI- and IRAG-deficient platelets. These results demonstrate that cCMP acts as intracellular messenger molecule, most unexpectedly utilizing the cGMP signal transduction pathway.
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