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Role of protein kinase C-dependent A-kinase anchoring proteins in lysophosphatidic acid-induced cAMP signaling in human diploid fibroblasts

Cited 8 time in Web of Science Cited 8 time in Scopus
Authors
Rhim, Ji-Heon; Jang, Ik-Sook; Yeo, Eui-Ju; Song, Kye-Yong; Park, Sang Chul
Issue Date
2006-11-04
Publisher
Wiley-Blackwell
Citation
Aging Cell. 2006 Dec;5(6):451-61. Epub 2006 Nov 1.
Keywords
A Kinase Anchor ProteinsAdaptor Proteins, Signal Transducing/*metabolismAdenylate Cyclase/metabolismAnimalsCell Aging/drug effects/*physiologyCell Cycle Proteins/*metabolismCells, CulturedCyclic AMP/*biosynthesisCyclic AMP-Dependent Protein Kinases/*metabolismDiploidyDown-Regulation/geneticsFibroblasts/drug effects/enzymology/metabolismHumansInfant, NewbornLysophospholipids/metabolism/pharmacologyMaleProtein Binding/physiologyProtein Kinase C-alpha/metabolismRNA InterferenceRatsSignal Transduction/drug effects/*physiologyUp-Regulation/drug effects/physiology
Abstract
Previously, we reported that lysophosphatidic acid (LPA)-induced adenosine 3',5'-cyclic monophosphate (cAMP) production by human diploid fibroblasts depends on the age of the fibroblasts. In this study, we examined the role of A-kinase anchoring proteins (AKAP) in the regulation of LPA-stimulated cAMP production in senescent fibroblasts. We found that levels of protein kinase C (PKC)-dependent AKAPs, such as Gravin and AKAP79, were elevated in senescent cells. Co-immunoprecipitation experiments revealed that Gravin and AKAP79 do not associate with adenylyl cyclase type 2 (AC2) but bind to AC4/6, which interacts with calcium-dependent PKCs alpha/beta both in young and senescent fibroblasts. When the expression of Gravin and AKAP79 was blocked by small interference RNA transfection, the basal level of cAMP was greatly reduced and the cAMP status after LPA treatment was also reversed. Protein kinase A showed a similar pattern in terms of its basal activity and LPA-dependent modulation. These data suggest that Gravin and to a lesser extent, AKAP79, may play important roles in maintaining the basal AC activity and in coupling the AC systems to inhibitory signals such as Gialpha in young cells, and to stimulatory signals such as PKCs in senescent cells. This study also demonstrates that Gravin is especially important for the long-term activation of PKC by LPA in senescent cells. We conclude that LPA-dependent increased level of cAMP in senescent human diploid fibroblasts is associated with increases in Gravin levels resulting in its increased binding with and activation of calcium-dependent PKC alpha/beta and AC4/6.
ISSN
1474-9718 (Print)
Language
English
URI
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=17081159

https://hdl.handle.net/10371/24369
DOI
https://doi.org/10.1111/j.1474-9726.2006.00239.x
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College of Medicine/School of Medicine (의과대학/대학원)Dept. of Biochemistry & Molecular Biology (생화학교실)Journal Papers (저널논문_생화학교실)
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