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Involvement of glycogen synthase kinase-3beta in palmitate-induced human umbilical vein endothelial cell apoptosis.

Authors
Choi, SE; Kang, Y; Jang, HJ; Shin, HC; Kim, HE; Kim, HS; Kim, HJ; Kim, DJ; Lee, KW
Citation
Journal of vascular research, 44(5):365-374, 2007
Journal Title
Journal of vascular research
ISSN
1018-11721423-0135
Abstract
BACKGROUND/AIMS: The death of endothelial cells may play a critical role in the development of various vascular diseases, including atherosclerosis. While free fatty acids (FFAs) may stimulate endothelial apoptosis, the molecular and cellular mechanisms of this effect have not been studied intensively. To elucidate the mechanisms involved in FFA-induced endothelial cell apoptosis, we investigated the effect of different pharmacological inhibitors on palmitate-induced apoptosis in human umbilical vein endothelial cells (HUVECs). Interestingly, lithium, a glycogen synthase kinase-3 (GSK-3) inhibitor, showed a strong protective effect. METHODS AND RESULTS: To examine the involvement of GSK-3beta in palmitate-induced HUVEC apoptosis, its dephosphorylation at Ser9 and enzymatic activation in response to palmitate treatment were monitored by immunoblotting and in vitro kinase assays, respectively. GSK-3beta was dephosphorylated and its enzymatic activity increased in palmitate-treated HUVECs. In addition, pretreatment with other GSK-3beta inhibitors, e.g. SB216763 or TDZD-8, as well as adenoviral transduction with a catalytically inactive GSK-3beta had significant protective effects against palmitate-induced HUVEC apoptosis. CONCLUSION: These results demonstrate that the GSK-3beta signalling pathway is involved in palmitate-induced HUVEC apoptosis.
MeSH terms
Adenoviridae/geneticsAnthracenes/pharmacologyApoptosis/drug effects*Caspase 3/metabolismCell Cycle/drug effectsCells, Cultured/cytologyCells, Cultured/drug effectsCytosol/chemistryEndothelial Cells/cytologyEndothelial Cells/drug effects*Endothelium, Vascular/cytology*Enzyme Activation/drug effectsFumonisins/pharmacologyGenetic Vectors/pharmacologyGlycogen Synthase Kinase 3/antagonists & inhibitorsGlycogen Synthase Kinase 3/geneticsGlycogen Synthase Kinase 3/physiology*HumansImidazoles/pharmacologyIndoles/pharmacologyLithium Chloride/pharmacologyMaleimides/pharmacologyMitochondria/chemistryPalmitates/pharmacology*PhosphorylationPhosphoserine/metabolismPoly(ADP-ribose) Polymerases/metabolismProtein Processing, Post-Translational/drug effectsPyridines/pharmacologyThiadiazoles/pharmacologyTransduction, GeneticUmbilical Veins
DOI
10.1159/000102321
PMID
17483602
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Endocrinology & Metabolism
Journal Papers > Research Organization > Chronic Inflammatory Disease Research Center
Journal Papers > School of Medicine / Graduate School of Medicine > Physiology
AJOU Authors
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