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PMID: 16125936 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

NPP-type ectophosphodiesterases: unity in diversity.

Trends in biochemical sciences ·Vol. 30 ·No. 10 ·2005-10-00 ·Pages 542-50

Stefan C, Jansen S, Bollen M

Abstract

Nucleotide pyrophosphatase/phosphodiesterase (NPP)-type ectophosphodiesterases are found at the cell surface as type-I or type-II transmembrane proteins, but are also found extracellularly as secreted or shedded enzymes. They hydrolyze pyrophosphate or phosphodiester bonds in a variety of extracellular compounds including nucleotides, (lyso)phospholipids and choline phosphate esters. Despite their structurally related catalytic domain, each enzyme has well-defined substrate specificity. Catalysis by NPPs affects processes as diverse as cell proliferation and motility, angiogenesis, bone mineralization and digestion. In addition, there is emerging evidence for non-catalytic functions of NPPs in cell signaling. NPP-type ectophosphodiesterases are also implicated in the pathophysiology of cancer, insulin resistance and calcification diseases, and they hold great promise as easily accessible therapeutic targets.

MeSH Terms
Animals Cell Movement Cell Proliferation Humans Neovascularization, Physiologic Phosphoric Diester Hydrolases/metabolism Pyrophosphatases/metabolism Signal Transduction Structure-Activity Relationship Substrate Specificity
Chemicals
Phosphoric Diester Hydrolases Pyrophosphatases nucleotide pyrophosphatase - phosphodiesterase I
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Stefan Cristiana
Afdeling Biochemie, Faculteit Geneeskunde, Katholieke Universiteit Leuven, B-3000 Leuven, Belgium.
Jansen Silvia
Bollen Mathieu
Article Info
Journal
Trends in biochemical sciences
Abbr.
Trends Biochem Sci
ISSN
0968-0004
Published
2005-10-00
Pages
542-50
Language
English
Region
England
NLM ID
7610674
Subset
IM
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