Editorial |
From the Department of Pathology, University of Washington School of Medicine, Seattle.
Correspondence to Karin E. Bornfeldt, Department of Pathology, Box 357470, University of Washington School of Medicine, Seattle, WA 98195-7470. E-mail bornf@u.washington.edu
See related article, pages 777784
Key Words: cyclic GMP cyclic nucleotide phosphodiestaerases cytoskeleton editorials proliferation smooth muscle cell
An extract of the first 250 words of the full text is provided, because this article has no abstract. |
| Introduction |
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and ß subunits. There are several isoforms of the
and ß subunit,
1ß1 being the most abundant combination in mammalian tissues.13 Soluble guanylyl cyclase is activated by nitric oxide (NO) and NO-releasing drugs. Particulate forms of guanylyl cyclase, on the other hand, are transmembrane proteins that are activated by the natriuretic peptides ANP, BNP, and CNP.4 Similarly, cGMP is degraded by a large number of cyclic nucleotide phosphodiesterases (PDEs). To date, 21 different PDE genes divided among 11 gene families have been identified in mammals. Most PDE families contain more than one gene, and most genes code for more than one mRNA. Although some PDE gene families hydrolyze cAMP exclusively (PDE4, PDE7, PDE8), many of these enzymes hydrolyze cGMP, or both cAMP and cGMP.5 PDE5 is the major cGMP-specific PDE gene family in some cell types. Other cGMP-hydrolyzing PDE gene families include PDE1, PDE2, PDE6, PDE9, PDE10, PDE11, and possibly PDE3.6 Any
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