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The Role of Synaptopodin in Membrane Protein Diffusion in the Dendritic Spine Neck

The dynamic exchange of neurotransmitter receptors at synapses relies on their lateral diffusion in the plasma membrane. At synapses located on dendritic spines this process is limited by the geometry of the spine neck that restricts the passage of membrane proteins. Biochemical compartmentalisation...

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Autores principales: Wang, Lili, Dumoulin, Andréa, Renner, Marianne, Triller, Antoine, Specht, Christian G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4739495/
https://www.ncbi.nlm.nih.gov/pubmed/26840625
http://dx.doi.org/10.1371/journal.pone.0148310
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author Wang, Lili
Dumoulin, Andréa
Renner, Marianne
Triller, Antoine
Specht, Christian G.
author_facet Wang, Lili
Dumoulin, Andréa
Renner, Marianne
Triller, Antoine
Specht, Christian G.
author_sort Wang, Lili
collection PubMed
description The dynamic exchange of neurotransmitter receptors at synapses relies on their lateral diffusion in the plasma membrane. At synapses located on dendritic spines this process is limited by the geometry of the spine neck that restricts the passage of membrane proteins. Biochemical compartmentalisation of the spine is believed to underlie the input-specificity of excitatory synapses and to set the scale on which functional changes can occur. Synaptopodin is located predominantly in the neck of dendritic spines, and is thus ideally placed to regulate the exchange of synaptic membrane proteins. The central aim of our study was to assess whether the presence of synaptopodin influences the mobility of membrane proteins in the spine neck and to characterise whether this was due to direct molecular interactions or to spatial constraints that are related to the structural organisation of the neck. Using single particle tracking we have identified a specific effect of synaptopodin on the diffusion of metabotropic mGluR5 receptors in the spine neck. However, super-resolution STORM/PALM imaging showed that this was not due to direct interactions between the two proteins, but that the presence of synaptopodin is associated with an altered local organisation of the F-actin cytoskeleton, that in turn could restrict the diffusion of membrane proteins with large intracellular domains through the spine neck. This study contributes new data on the way in which the spine neck compartmentalises excitatory synapses. Our data complement models that consider the impact of the spine neck as a function of its shape, by showing that the internal organisation of the neck imposes additional physical barriers to membrane protein diffusion.
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spelling pubmed-47394952016-02-11 The Role of Synaptopodin in Membrane Protein Diffusion in the Dendritic Spine Neck Wang, Lili Dumoulin, Andréa Renner, Marianne Triller, Antoine Specht, Christian G. PLoS One Research Article The dynamic exchange of neurotransmitter receptors at synapses relies on their lateral diffusion in the plasma membrane. At synapses located on dendritic spines this process is limited by the geometry of the spine neck that restricts the passage of membrane proteins. Biochemical compartmentalisation of the spine is believed to underlie the input-specificity of excitatory synapses and to set the scale on which functional changes can occur. Synaptopodin is located predominantly in the neck of dendritic spines, and is thus ideally placed to regulate the exchange of synaptic membrane proteins. The central aim of our study was to assess whether the presence of synaptopodin influences the mobility of membrane proteins in the spine neck and to characterise whether this was due to direct molecular interactions or to spatial constraints that are related to the structural organisation of the neck. Using single particle tracking we have identified a specific effect of synaptopodin on the diffusion of metabotropic mGluR5 receptors in the spine neck. However, super-resolution STORM/PALM imaging showed that this was not due to direct interactions between the two proteins, but that the presence of synaptopodin is associated with an altered local organisation of the F-actin cytoskeleton, that in turn could restrict the diffusion of membrane proteins with large intracellular domains through the spine neck. This study contributes new data on the way in which the spine neck compartmentalises excitatory synapses. Our data complement models that consider the impact of the spine neck as a function of its shape, by showing that the internal organisation of the neck imposes additional physical barriers to membrane protein diffusion. Public Library of Science 2016-02-03 /pmc/articles/PMC4739495/ /pubmed/26840625 http://dx.doi.org/10.1371/journal.pone.0148310 Text en © 2016 Wang et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Wang, Lili
Dumoulin, Andréa
Renner, Marianne
Triller, Antoine
Specht, Christian G.
The Role of Synaptopodin in Membrane Protein Diffusion in the Dendritic Spine Neck
title The Role of Synaptopodin in Membrane Protein Diffusion in the Dendritic Spine Neck
title_full The Role of Synaptopodin in Membrane Protein Diffusion in the Dendritic Spine Neck
title_fullStr The Role of Synaptopodin in Membrane Protein Diffusion in the Dendritic Spine Neck
title_full_unstemmed The Role of Synaptopodin in Membrane Protein Diffusion in the Dendritic Spine Neck
title_short The Role of Synaptopodin in Membrane Protein Diffusion in the Dendritic Spine Neck
title_sort role of synaptopodin in membrane protein diffusion in the dendritic spine neck
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4739495/
https://www.ncbi.nlm.nih.gov/pubmed/26840625
http://dx.doi.org/10.1371/journal.pone.0148310
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