- Meeting abstract
- Open Access
Interaction of cCMP with the cGK, cAK and MAPK kinases in murine tissues
© Wolfertstetter et al. 2015
- Published: 2 September 2015
- MAPK Signaling
- Cyclic Nucleotide
- MAPK Signaling Pathway
- MAPK Phosphorylation
- MAPK Kinase
cAMP and cGMP are well established second messengers that are essential for numerous of (patho)physiological processes. These purine cyclic nucleotides activate cAK and cGK, respectively. So far, there was no evidence of further cyclic nucleotides acting as second messengers. Meanwhile the existence of cCMP was described [1, 2]. cCMP activates the purified cyclic nucleotide-dependent protein kinases cAK and cGK and induces relaxation of vascular smooth muscle via cGKI . Furthermore, it was postulated that cCMP is relevant for cell growth  and blood cell function . However, functions regulated by cCMP are mostly unknown.
To elucidate propable functions cCMP-binding and -activated proteins were identified using different methods. Competitive binding assays identified cAK, cGKI, and cGKII as cCMP-binding proteins in murine tissue lysates, using 4-AH-cCMP agarose. cCMP (200 µM) was added (+) or omitted (-) during the affinity chromatography experiments to investigate the specificity of the binding. An interaction between cCMP/MAPK and a protein-protein complex of MAPK/cGK were detected via cCMP affinity chromatography and co-immunoprecipitation, respectively. Interestingly, no specific interaction of MAPK with 8-AET-cGMP agarose was detected. Moreover, DB-cCMP (100 µM) was also able to stimulate the phosphorylation of p44/p42 MAPK. The phosphorylation of MAPK was inhibited by the addition of the PKA inhibitor AS5-24, suggesting a stimulatory function for PKA in cCMP-mediated MAPK phosphorylation. To elucidate the role of cGK in murine tissues in this process, we used cGKII knockout (cGKII KO) and cGKI knockout (cGKI KO) mice. We detected stimulation in the jejunum tissues from cGKI KO and cGKII KO mice. It is interesting to note that the phosphorylation in the jejunum cGKII KO tissue was significantly increased when compared with the WT and cGKI KO tissues, suggesting an inhibitory role for cGKII in cCMP-induced MAPK phosphorylation in the jejunum.
These results suggest that MAPK signaling is regulated by cGMP-dependent protein kinases upon activation by cCMP. Hence, cCMP could potentially act as a second messenger in the cAK/cGK and MAPK signaling pathways and play an important role in physiological processes of the jejunum.
This work was supported by the Bavarian state.
- Newton RP, Salih SG, Salvage BJ, Kingston EE: Extraction, purification and identification of cytidine 3',5'-cyclic monophosphate from rat tissues. Biochem J. 1984, 221 (3): 665-673.View ArticlePubMedPubMed CentralGoogle Scholar
- Bähre H, Hartwig C, Munder A, Wolter S, Stelzer T, Schirmer B, et al: cCMP and cUMP occur in vivo. Biochem Biophys Res Commun. 2015, 460 (4): 909-914. 10.1016/j.bbrc.2015.03.115.View ArticlePubMedPubMed CentralGoogle Scholar
- Desch M, Schinner E, Kees F, Hofmann F, Seifert R, Schlossmann: Cyclic cytidine 3',5'-monophosphate (cCMP) signals via cGMP kinase I. FEBS Lett. 2010, 584 (18): 3979-3984. 10.1016/j.febslet.2010.07.059.View ArticlePubMedGoogle Scholar
- Cheng YC, Bloch A: Demonstration, in leukemia L-1210 cells, of a phosphodiesterase acting on 3':5'-cyclic CMP but not on 3':5'-cyclic AMP or 3':5'-cyclic GMP. J Biol Chem. 1978, 253 (8): 2522-2524.PubMedGoogle Scholar
- Ervens J, Seifert R: Differential modulation by N4, 2'-O-dibutyryl cytidine 3':5'-cyclic monophosphate of neutrophil activation. Biochem Biophys Res Commun. 1991, 174 (1): 258-267. 10.1016/0006-291X(91)90514-8.View ArticlePubMedGoogle Scholar
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