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      Role of glycogen synthase kinase-3 in the phosphatidylinositol 3-Kinase/Akt cell survival pathway.

      The Journal of Biological Chemistry
      Animals, Apoptosis, genetics, Calcium-Calmodulin-Dependent Protein Kinases, physiology, Cell Survival, Chromones, pharmacology, Cysteine Proteinase Inhibitors, Gene Expression Regulation, Glycogen Synthase Kinase 3, Glycogen Synthase Kinases, Microscopy, Fluorescence, Morpholines, Nerve Growth Factors, Oligopeptides, PC12 Cells, Phosphatidylinositol 3-Kinases, antagonists & inhibitors, metabolism, Protein-Serine-Threonine Kinases, Rats, Transfection

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          Abstract

          Growth factor-dependent survival of a variety of mammalian cells is dependent on the activation of phosphatidylinositol (PI) 3-kinase and its downstream effector, the protein kinase Akt. Glycogen synthase kinase-3 (GSK-3) has been previously identified as a physiological target of Akt, which is inhibited by phosphorylation, so we have investigated the role of GSK-3 in cell survival. Overexpression of catalytically active GSK-3 induced apoptosis of both Rat-1 and PC12 cells, whereas dominant-negative GSK-3 prevented apoptosis following inhibition of PI 3-kinase. GSK-3 thus plays a critical role in regulation of apoptosis and represents a key downstream target of the PI 3-kinase/Akt survival signaling pathway.

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