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  Depolarization drives beta-Catenin into neuronal spines promoting changes in synaptic structure and function

Murase, S., Mosser, E., & Schuman, E. M. (2002). Depolarization drives beta-Catenin into neuronal spines promoting changes in synaptic structure and function. Neuron, 35(1), 91-105. doi:10.1016/s0896-6273(02)00764-x.

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Murase, S., Author
Mosser, E., Author
Schuman, Erin M.1, Author           
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1Synaptic Plasticity Department, Max Planck Institute for Brain Research, Max Planck Society, ou_2461710              

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Free keywords: Animals Animals, Newborn Cadherins/metabolism Cells, Cultured Cytoskeletal Proteins/drug effects/genetics/*metabolism Dendrites/drug effects/*metabolism/ultrastructure Disks Large Homolog 4 Protein Enzyme Inhibitors/pharmacology Fluorescent Dyes Green Fluorescent Proteins Hippocampus/cytology/*growth & development/*metabolism Indicators and Reagents/metabolism Intracellular Signaling Peptides and Proteins Luminescent Proteins/metabolism Male Membrane Potentials/drug effects/physiology Membrane Proteins Mutation/genetics Nerve Tissue Proteins/metabolism Neuronal Plasticity/drug effects/*genetics Potassium Chloride/pharmacology Protein Transport/drug effects/*genetics Protein-Tyrosine Kinases/antagonists & inhibitors/metabolism Pyridinium Compounds Quaternary Ammonium Compounds Rats Recombinant Fusion Proteins Synapses/drug effects/*metabolism/ultrastructure Synapsins/metabolism Synaptic Transmission/drug effects/*genetics *Trans-Activators Tyrosine/genetics/metabolism beta Catenin
 Abstract: Activity-induced changes in adhesion molecules may coordinate presynaptic and postsynaptic plasticity. Here, we demonstrate that beta-catenin, which mediates interactions between cadherins and the actin cytoskeleton, moves from dendritic shafts into spines upon depolarization, increasing its association with cadherins. beta-catenin's redistribution was mimicked or prevented by a tyrosine kinase or phosphatase inhibitor, respectively. Point mutations of beta-catenin's tyrosine 654 altered the shaft/spine distribution: Y654F-beta-catenin-GFP (phosphorylation-prevented) was concentrated in spines, whereas Y654E-beta-catenin-GFP (phosphorylation-mimic) accumulated in dendritic shafts. In Y654F-expressing neurons, the PSD-95 or associated synapsin-I clusters were larger than those observed in either wild-type-beta-catenin or also Y654E-expressing neurons. Y654F-expressing neurons exhibited a higher minifrequency. Thus, neural activity induces beta-catenin's redistribution into spines, where it interacts with cadherin to influence synaptic size and strength.

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 Dates: 2002-07-19
 Publication Status: Issued
 Pages: -
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 Identifiers: Other: 12123611
DOI: 10.1016/s0896-6273(02)00764-x
ISSN: 0896-6273 (Print)0896-6273 (Linking)
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Title: Neuron
Source Genre: Journal
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Pages: - Volume / Issue: 35 (1) Sequence Number: - Start / End Page: 91 - 105 Identifier: -