| Literature DB >> 17320989 |
Rebecka Lindh1, Faiyaz Ahmad, Svante Resjö, Peter James, Jeong S Yang, Henry M Fales, Vincent Manganiello, Eva Degerman.
Abstract
Phosphodiesterase 3B (PDE3B) is an important component of insulin and cAMP-dependent signalling pathways. In order to study phosphorylation of PDE3B, we have used an adenoviral system to express recombinant flag-tagged PDE3B in primary rat adipocytes and H4IIE hepatoma cells. Phosphorylation of PDE3B after treatment of cells with insulin, cAMP-increasing agents, or the phosphatase inhibitor, calyculin A was analyzed by two-dimensional tryptic phosphopeptide mapping and mass spectrometry. We found that PDE3B is multisite phosphorylated in adipocytes and H4IIE hepatoma cells in response to all these stimuli. Several sites were identified; serine (S)273, S296, S421, S424/5, S474 and S536 were phosphorylated in adipocyte as well as H4IIE hepatoma cells whereas S277 and S507 were phosphorylated in hepatoma cells only. Several of the sites were phosphorylated by insulin as well as cAMP-increasing hormones indicating integration of the two signalling pathways upstream of PDE3B, maybe at the level of protein kinase B.Entities:
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Year: 2007 PMID： 17320989 DOI： 10.1016/j.bbamcr.2007.01.010
Source DB: PubMed Journal: Biochim Biophys Acta ISSN： 0006-3002