Meeting Report: cGMP MattersA report on the 3rd International Conference on cGMP Generators, Effectors and Therapeutic Implications, Dresden, Germany, 15 to 17 June 2007.

Author:

Kemp-Harper Barbara1,Feil Robert2

Affiliation:

1. Department of Pharmacology and Centre for Vascular Health, Monash University, Clayton, Victoria, Australia.

2. Interfakultäres Institut für Biochemie, Universität Tübingen, Tübingen, Germany.

Abstract

The second messenger cyclic guanosine 3′,5′-monophosphate (cGMP) controls many cellular functions ranging from growth to contractility. Generated from guanylyl cyclases in response to natriuretic peptides or nitric oxide, cGMP transduces its effects through a number of cGMP effectors, including cGMP-regulated phosphodiesterases and protein kinases. Drugs that modulate cGMP levels are emerging as promising therapies, particularly for cardiovascular disorders. This report summarizes new data on the molecular mechanisms, (patho)physiological relevance, and therapeutic potential of the cGMP signaling system that were presented at the 3rd cGMP meeting held in June 2007 in Dresden, Germany.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference47 articles.

1. cGMP signalling: from bench to bedside

2. The 3rd International Conference on cGMP Generators Effectors and Therapeutic Implications took place in Dresden Germany 15 to 17 June 2007 and was organized by F. Hofmann H. Schmidt and J. P. Stasch. The next cGMP meeting will be held in Regensburg Germany in June 2009.

3. Regulation of Nitric Oxide-Sensitive Guanylyl Cyclase

4. Identification of Residues Crucially Involved in the Binding of the Heme Moiety of Soluble Guanylate Cyclase

5. Dimerization Region of Soluble Guanylate Cyclase Characterized by Bimolecular Fluorescence Complementation in Vivo

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