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Myosin V regulates synaptopodin clustering and localization in the dendrites of hippocampal neurons

The spine apparatus (SA) is an endoplasmic reticulum-related organelle that is present in a subset of dendritic spines in cortical and pyramidal neurons, and plays an important role in Ca(2+) homeostasis and dendritic spine plasticity. The protein synaptopodin is essential for the formation of the S...

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Autores principales: Konietzny, Anja, González-Gallego, Judit, Bär, Julia, Perez-Alvarez, Alberto, Drakew, Alexander, Demmers, Jeroen A. A., Dekkers, Dick H. W., Hammer, John A., Frotscher, Michael, Oertner, Thomas G., Wagner, Wolfgang, Kneussel, Matthias, Mikhaylova, Marina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6737913/
https://www.ncbi.nlm.nih.gov/pubmed/31371487
http://dx.doi.org/10.1242/jcs.230177
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author Konietzny, Anja
González-Gallego, Judit
Bär, Julia
Perez-Alvarez, Alberto
Drakew, Alexander
Demmers, Jeroen A. A.
Dekkers, Dick H. W.
Hammer, John A.
Frotscher, Michael
Oertner, Thomas G.
Wagner, Wolfgang
Kneussel, Matthias
Mikhaylova, Marina
author_facet Konietzny, Anja
González-Gallego, Judit
Bär, Julia
Perez-Alvarez, Alberto
Drakew, Alexander
Demmers, Jeroen A. A.
Dekkers, Dick H. W.
Hammer, John A.
Frotscher, Michael
Oertner, Thomas G.
Wagner, Wolfgang
Kneussel, Matthias
Mikhaylova, Marina
author_sort Konietzny, Anja
collection PubMed
description The spine apparatus (SA) is an endoplasmic reticulum-related organelle that is present in a subset of dendritic spines in cortical and pyramidal neurons, and plays an important role in Ca(2+) homeostasis and dendritic spine plasticity. The protein synaptopodin is essential for the formation of the SA and is widely used as a maker for this organelle. However, it is still unclear which factors contribute to its localization at selected synapses, and how it triggers local SA formation. In this study, we characterized development, localization and mobility of synaptopodin clusters in hippocampal primary neurons, as well as the molecular dynamics within these clusters. Interestingly, synaptopodin at the shaft-associated clusters is less dynamic than at spinous clusters. We identify the actin-based motor proteins myosin V (herein referring to both the myosin Va and Vb forms) and VI as novel interaction partners of synaptopodin, and demonstrate that myosin V is important for the formation and/or maintenance of the SA. We found no evidence of active microtubule-based transport of synaptopodin. Instead, new clusters emerge inside spines, which we interpret as the SA being assembled on-site.
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spelling pubmed-67379132019-10-02 Myosin V regulates synaptopodin clustering and localization in the dendrites of hippocampal neurons Konietzny, Anja González-Gallego, Judit Bär, Julia Perez-Alvarez, Alberto Drakew, Alexander Demmers, Jeroen A. A. Dekkers, Dick H. W. Hammer, John A. Frotscher, Michael Oertner, Thomas G. Wagner, Wolfgang Kneussel, Matthias Mikhaylova, Marina J Cell Sci Research Article The spine apparatus (SA) is an endoplasmic reticulum-related organelle that is present in a subset of dendritic spines in cortical and pyramidal neurons, and plays an important role in Ca(2+) homeostasis and dendritic spine plasticity. The protein synaptopodin is essential for the formation of the SA and is widely used as a maker for this organelle. However, it is still unclear which factors contribute to its localization at selected synapses, and how it triggers local SA formation. In this study, we characterized development, localization and mobility of synaptopodin clusters in hippocampal primary neurons, as well as the molecular dynamics within these clusters. Interestingly, synaptopodin at the shaft-associated clusters is less dynamic than at spinous clusters. We identify the actin-based motor proteins myosin V (herein referring to both the myosin Va and Vb forms) and VI as novel interaction partners of synaptopodin, and demonstrate that myosin V is important for the formation and/or maintenance of the SA. We found no evidence of active microtubule-based transport of synaptopodin. Instead, new clusters emerge inside spines, which we interpret as the SA being assembled on-site. The Company of Biologists Ltd 2019-08-15 2019-08-22 /pmc/articles/PMC6737913/ /pubmed/31371487 http://dx.doi.org/10.1242/jcs.230177 Text en © 2019. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/4.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Konietzny, Anja
González-Gallego, Judit
Bär, Julia
Perez-Alvarez, Alberto
Drakew, Alexander
Demmers, Jeroen A. A.
Dekkers, Dick H. W.
Hammer, John A.
Frotscher, Michael
Oertner, Thomas G.
Wagner, Wolfgang
Kneussel, Matthias
Mikhaylova, Marina
Myosin V regulates synaptopodin clustering and localization in the dendrites of hippocampal neurons
title Myosin V regulates synaptopodin clustering and localization in the dendrites of hippocampal neurons
title_full Myosin V regulates synaptopodin clustering and localization in the dendrites of hippocampal neurons
title_fullStr Myosin V regulates synaptopodin clustering and localization in the dendrites of hippocampal neurons
title_full_unstemmed Myosin V regulates synaptopodin clustering and localization in the dendrites of hippocampal neurons
title_short Myosin V regulates synaptopodin clustering and localization in the dendrites of hippocampal neurons
title_sort myosin v regulates synaptopodin clustering and localization in the dendrites of hippocampal neurons
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6737913/
https://www.ncbi.nlm.nih.gov/pubmed/31371487
http://dx.doi.org/10.1242/jcs.230177
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