101. Phosphorylation of eukaryotic translation initiation factor 2Bepsilon by glycogen synthase kinase-3beta regulates beta-adrenergic cardiac myocyte hypertrophy.
- Author
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Hardt SE, Tomita H, Katus HA, and Sadoshima J
- Subjects
- Adenoviridae genetics, Adrenergic beta-Agonists pharmacology, Adrenergic beta-Antagonists pharmacology, Animals, Animals, Newborn, Atrial Natriuretic Factor biosynthesis, Atrial Natriuretic Factor genetics, Cardiomegaly enzymology, Cardiomegaly etiology, Cardiomegaly pathology, Cells, Cultured drug effects, Cells, Cultured enzymology, Gene Expression Regulation physiology, Genetic Vectors genetics, Glycogen Synthase Kinase 3 genetics, Glycogen Synthase Kinase 3 beta, Heart Ventricles cytology, Hypertrophy, Isoproterenol pharmacology, Lithium Chloride pharmacology, Male, Myocardial Infarction complications, Myocytes, Cardiac pathology, Myosin Heavy Chains biosynthesis, Myosin Heavy Chains genetics, Peptide Chain Initiation, Translational physiology, Phosphoserine metabolism, Propranolol pharmacology, Rats, Rats, Wistar, Recombinant Fusion Proteins physiology, Transduction, Genetic, Ventricular Remodeling physiology, Eukaryotic Initiation Factor-2B metabolism, Glycogen Synthase Kinase 3 physiology, Myocytes, Cardiac enzymology, Protein Processing, Post-Translational
- Abstract
Glycogen synthase kinase 3beta (GSK-3beta) negatively regulates cardiac hypertrophy. A potential target mediating the antihypertrophic effect of GSK-3beta is eukaryotic translation initiation factor 2Bepsilon (eIF2Bepsilon). Overexpression of GSK-3beta increased the cellular kinase activity toward GST-eIF2Bepsilon in neonatal rat cardiac myocytes, whereas LiCl (10 mmol/L) or isoproterenol (ISO) (10 micromol/L), a treatment known to inhibit GSK-3beta, decreased it. Immunoblot analyses using anti-S535 phosphospecific eIF2Bepsilon antibody showed that S535 phosphorylation of endogenous eIF2Bepsilon was decreased by LiCl or ISO, suggesting that GSK-3beta is the predominant kinase regulating phosphorylation of eIF2Bepsilon-S535 in cardiac myocytes. Decreases in eIF2Bepsilon-S535 phosphorylation were also observed in a rat model of cardiac hypertrophy in vivo. Overexpression of wild-type eIF2Bepsilon alone moderately increased cell size (+31+/-11%; P<0.05 versus control), whereas treatment of eIF2Bepsilon-transduced myocytes with LiCl (+73+/-22% versus eIF2Bepsilon only; P<0.05) or ISO (+84+/-33% versus eIF2Bepsilon only; P<0.05) enhanced the effect of eIF2Bepsilon. Overexpression of eIF2Bepsilon-S535A, which is not phosphorylated by GSK-3beta, increased cell size (+107+/-35%) as strongly as ISO (+95+/-25%), and abolished antihypertrophic effects of GSK-3beta, indicating that S535 phosphorylation of eIF2Bepsilon critically mediates antihypertrophic effects of GSK-3beta. Furthermore, expression of eIF2Bepsilon-F259L, a dominant-negative mutant, inhibited ISO-induced hypertrophy, indicating that eIF2Bepsilon is required for beta-adrenergic hypertrophy. Interestingly, expression of eIF2Bepsilon-S535A partially increased cytoskeletal reorganization, whereas it did not increase expression of atrial natriuretic factor gene. These results suggest that GSK-3beta is the predominant kinase mediating phosphorylation of eIF2Bepsilon-S535 in cardiac myocytes, which in turn plays an important role in regulating cardiac hypertrophy primarily through protein synthesis.
- Published
- 2004
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