Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2007-2-19
pubmed:abstractText
Contraction and relaxation of vascular smooth muscle and cardiac myocytes are key physiological events in the cardiovascular system. These events are regulated by second messengers, cAMP and cGMP, in response to extracellular stimulants. The strength of signal transduction is controlled by intracellular cyclic nucleotide concentrations, which are determined by a balance in production and degradation of cAMP and cGMP. Degradation of cyclic nucleotides is catalyzed by 3',5'-cyclic nucleotide phosphodiesterases (PDEs), and therefore regulation of PDEs hydrolytic activity is important for modulation of cellular functions. Mammalian PDEs are composed of 21 genes and are categorized into 11 families based on sequence homology, enzymatic properties, and sensitivity to inhibitors. PDE families contain many splice variants that mostly are unique in tissue-expression patterns, gene regulation, enzymatic regulation by phosphorylation and regulatory proteins, subcellular localization, and interaction with association proteins. Each unique variant is closely related to the regulation of a specific cellular signaling. Thus, multiple PDEs function as a particular modulator of each cardiovascular function and regulate physiological homeostasis.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
1524-4571
pubmed:author
pubmed:issnType
Electronic
pubmed:day
16
pubmed:volume
100
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
309-27
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:17307970-Animals, pubmed-meshheading:17307970-Binding Sites, pubmed-meshheading:17307970-Cyclic AMP, pubmed-meshheading:17307970-Cyclic AMP-Dependent Protein Kinases, pubmed-meshheading:17307970-Cyclic GMP, pubmed-meshheading:17307970-Female, pubmed-meshheading:17307970-Gene Expression Regulation, Enzymologic, pubmed-meshheading:17307970-Humans, pubmed-meshheading:17307970-Isoenzymes, pubmed-meshheading:17307970-Male, pubmed-meshheading:17307970-Mammals, pubmed-meshheading:17307970-Mice, pubmed-meshheading:17307970-Mice, Knockout, pubmed-meshheading:17307970-Mice, Transgenic, pubmed-meshheading:17307970-Models, Biological, pubmed-meshheading:17307970-Muscle, Smooth, Vascular, pubmed-meshheading:17307970-Muscle Cells, pubmed-meshheading:17307970-Muscle Contraction, pubmed-meshheading:17307970-Myocardial Contraction, pubmed-meshheading:17307970-Myocytes, Cardiac, pubmed-meshheading:17307970-Phenotype, pubmed-meshheading:17307970-Phosphoproteins, pubmed-meshheading:17307970-Phosphoric Diester Hydrolases, pubmed-meshheading:17307970-Phosphorylation, pubmed-meshheading:17307970-Phylogeny, pubmed-meshheading:17307970-Protein Interaction Mapping, pubmed-meshheading:17307970-Protein Kinases, pubmed-meshheading:17307970-Protein Processing, Post-Translational, pubmed-meshheading:17307970-Protein Structure, Tertiary, pubmed-meshheading:17307970-Rats, pubmed-meshheading:17307970-Signal Transduction, pubmed-meshheading:17307970-Subcellular Fractions
pubmed:year
2007
pubmed:articleTitle
Overview of PDEs and their regulation.
pubmed:affiliation
Discovery Research Laboratories, Tanabe Seiyaku Co Ltd, 2-50 Kawagishi 2-chome, Toda, Saitama 335-8505, Japan. k-omori@tanabe.co.jp
pubmed:publicationType
Journal Article, Review, Research Support, Non-U.S. Gov't