
Role of protein kinase C‐dependent A‐kinase anchoring proteins in lysophosphatidic acid‐induced cAMP signaling in human diploid fibroblasts
Author(s) -
Rhim JiHeon,
Jang IkSoon,
Yeo EuiJu,
Song KyeYong,
Park Sang Chul
Publication year - 2006
Publication title -
aging cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.103
H-Index - 140
eISSN - 1474-9726
pISSN - 1474-9718
DOI - 10.1111/j.1474-9726.2006.00239.x
Subject(s) - lysophosphatidic acid , biology , protein kinase c , protein kinase a , microbiology and biotechnology , adenylyl cyclase , kinase , immunoprecipitation , cyclic adenosine monophosphate , signal transduction , biochemistry , receptor , gene
Summary 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 a nchoring 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 α/β 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 Giα 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 α/β and AC4/6.