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      Reelin-mediated signaling locally regulates protein kinase B/Akt and glycogen synthase kinase 3beta.

      The Journal of Biological Chemistry
      Animals, Brain, embryology, enzymology, Cell Adhesion Molecules, Neuronal, metabolism, Cell Line, Enzyme Inhibitors, pharmacology, Extracellular Matrix Proteins, Gene Expression Regulation, Enzymologic, Glycogen Synthase Kinase 3, Homozygote, Humans, Immunoblotting, Immunohistochemistry, Mice, Mice, Inbred C57BL, Models, Biological, Nerve Tissue Proteins, Phosphatidylinositol 3-Kinases, Phosphorylation, Precipitin Tests, Protein Binding, Protein-Serine-Threonine Kinases, Proto-Oncogene Proteins, Proto-Oncogene Proteins c-akt, Rats, Recombinant Proteins, Serine, Serine Endopeptidases, Signal Transduction, Subcellular Fractions, Threonine, Transfection

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          Abstract

          Reelin is a large secreted protein that controls cortical layering by signaling through the very low density lipoprotein receptor and apolipoprotein E receptor 2, thereby inducing tyrosine phosphorylation of the adaptor protein Disabled-1 (Dab1) and suppressing tau phosphorylation in vivo. Here we show that binding of Reelin to these receptors stimulates phosphatidylinositol 3-kinase, resulting in activation of protein kinase B and inhibition of glycogen synthase kinase 3beta. We present genetic evidence that this cascade is dependent on apolipoprotein E receptor 2, very low density lipoprotein receptor, and Dab1. Reelin-signaling components are enriched in axonal growth cones, where tyrosine phosphorylation of Dab1 is increased in response to Reelin. These findings suggest that Reelin-mediated phosphatidylinositol 3-kinase signaling in neuronal growth cones contributes to final neuron positioning in the mammalian brain by local modulation of protein kinase B and glycogen synthase kinase 3beta kinase activities.

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