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EVL and MIM/MTSS1 regulate actin cytoskeletal remodeling to promote dendritic filopodia in neurons
Dendritic spines are the postsynaptic compartment of a neuronal synapse and are critical for synaptic connectivity and plasticity. A developmental precursor to dendritic spines, dendritic filopodia (DF), facilitate synapse formation by sampling the environment for suitable axon partners during neuro...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9998662/ https://www.ncbi.nlm.nih.gov/pubmed/36828364 http://dx.doi.org/10.1083/jcb.202106081 |
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author | Parker, Sara S. Ly, Kenneth Tran Grant, Adam D. Sweetland, Jillian Wang, Ashley M. Parker, James D. Roman, Mackenzie R. Saboda, Kathylynn Roe, Denise J. Padi, Megha Wolgemuth, Charles W. Langlais, Paul Mouneimne, Ghassan |
author_facet | Parker, Sara S. Ly, Kenneth Tran Grant, Adam D. Sweetland, Jillian Wang, Ashley M. Parker, James D. Roman, Mackenzie R. Saboda, Kathylynn Roe, Denise J. Padi, Megha Wolgemuth, Charles W. Langlais, Paul Mouneimne, Ghassan |
author_sort | Parker, Sara S. |
collection | PubMed |
description | Dendritic spines are the postsynaptic compartment of a neuronal synapse and are critical for synaptic connectivity and plasticity. A developmental precursor to dendritic spines, dendritic filopodia (DF), facilitate synapse formation by sampling the environment for suitable axon partners during neurodevelopment and learning. Despite the significance of the actin cytoskeleton in driving these dynamic protrusions, the actin elongation factors involved are not well characterized. We identified the Ena/VASP protein EVL as uniquely required for the morphogenesis and dynamics of DF. Using a combination of genetic and optogenetic manipulations, we demonstrated that EVL promotes protrusive motility through membrane-direct actin polymerization at DF tips. EVL forms a complex at nascent protrusions and DF tips with MIM/MTSS1, an I-BAR protein important for the initiation of DF. We proposed a model in which EVL cooperates with MIM to coalesce and elongate branched actin filaments, establishing the dynamic lamellipodia-like architecture of DF. |
format | Online Article Text |
id | pubmed-9998662 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-99986622023-03-11 EVL and MIM/MTSS1 regulate actin cytoskeletal remodeling to promote dendritic filopodia in neurons Parker, Sara S. Ly, Kenneth Tran Grant, Adam D. Sweetland, Jillian Wang, Ashley M. Parker, James D. Roman, Mackenzie R. Saboda, Kathylynn Roe, Denise J. Padi, Megha Wolgemuth, Charles W. Langlais, Paul Mouneimne, Ghassan J Cell Biol Article Dendritic spines are the postsynaptic compartment of a neuronal synapse and are critical for synaptic connectivity and plasticity. A developmental precursor to dendritic spines, dendritic filopodia (DF), facilitate synapse formation by sampling the environment for suitable axon partners during neurodevelopment and learning. Despite the significance of the actin cytoskeleton in driving these dynamic protrusions, the actin elongation factors involved are not well characterized. We identified the Ena/VASP protein EVL as uniquely required for the morphogenesis and dynamics of DF. Using a combination of genetic and optogenetic manipulations, we demonstrated that EVL promotes protrusive motility through membrane-direct actin polymerization at DF tips. EVL forms a complex at nascent protrusions and DF tips with MIM/MTSS1, an I-BAR protein important for the initiation of DF. We proposed a model in which EVL cooperates with MIM to coalesce and elongate branched actin filaments, establishing the dynamic lamellipodia-like architecture of DF. Rockefeller University Press 2023-02-24 /pmc/articles/PMC9998662/ /pubmed/36828364 http://dx.doi.org/10.1083/jcb.202106081 Text en © 2023 Parker et al. https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Parker, Sara S. Ly, Kenneth Tran Grant, Adam D. Sweetland, Jillian Wang, Ashley M. Parker, James D. Roman, Mackenzie R. Saboda, Kathylynn Roe, Denise J. Padi, Megha Wolgemuth, Charles W. Langlais, Paul Mouneimne, Ghassan EVL and MIM/MTSS1 regulate actin cytoskeletal remodeling to promote dendritic filopodia in neurons |
title | EVL and MIM/MTSS1 regulate actin cytoskeletal remodeling to promote dendritic filopodia in neurons |
title_full | EVL and MIM/MTSS1 regulate actin cytoskeletal remodeling to promote dendritic filopodia in neurons |
title_fullStr | EVL and MIM/MTSS1 regulate actin cytoskeletal remodeling to promote dendritic filopodia in neurons |
title_full_unstemmed | EVL and MIM/MTSS1 regulate actin cytoskeletal remodeling to promote dendritic filopodia in neurons |
title_short | EVL and MIM/MTSS1 regulate actin cytoskeletal remodeling to promote dendritic filopodia in neurons |
title_sort | evl and mim/mtss1 regulate actin cytoskeletal remodeling to promote dendritic filopodia in neurons |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9998662/ https://www.ncbi.nlm.nih.gov/pubmed/36828364 http://dx.doi.org/10.1083/jcb.202106081 |
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