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Exploring new roles for actin upon LTP induction in dendritic spines

Dendritic spines, small protrusions of the dendrites, enlarge upon LTP induction, linking morphological and functional properties. Although the role of actin in spine enlargement has been well studied, little is known about its relationship with mechanical membrane properties, such as membrane tensi...

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Autores principales: Bonilla-Quintana, Mayte, Wörgötter, Florentin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8007616/
https://www.ncbi.nlm.nih.gov/pubmed/33782451
http://dx.doi.org/10.1038/s41598-021-86367-z
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author Bonilla-Quintana, Mayte
Wörgötter, Florentin
author_facet Bonilla-Quintana, Mayte
Wörgötter, Florentin
author_sort Bonilla-Quintana, Mayte
collection PubMed
description Dendritic spines, small protrusions of the dendrites, enlarge upon LTP induction, linking morphological and functional properties. Although the role of actin in spine enlargement has been well studied, little is known about its relationship with mechanical membrane properties, such as membrane tension, which is involved in many cell processes, like exocytosis. Here, we use a 3D model of the dendritic spine to investigate how polymerization of actin filaments can effectively elevate the membrane tension to trigger exocytosis in a domain close to the tip of the spine. Moreover, we show that the same pool of actin promotes full membrane fusion after exocytosis and spine stabilization.
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spelling pubmed-80076162021-03-30 Exploring new roles for actin upon LTP induction in dendritic spines Bonilla-Quintana, Mayte Wörgötter, Florentin Sci Rep Article Dendritic spines, small protrusions of the dendrites, enlarge upon LTP induction, linking morphological and functional properties. Although the role of actin in spine enlargement has been well studied, little is known about its relationship with mechanical membrane properties, such as membrane tension, which is involved in many cell processes, like exocytosis. Here, we use a 3D model of the dendritic spine to investigate how polymerization of actin filaments can effectively elevate the membrane tension to trigger exocytosis in a domain close to the tip of the spine. Moreover, we show that the same pool of actin promotes full membrane fusion after exocytosis and spine stabilization. Nature Publishing Group UK 2021-03-29 /pmc/articles/PMC8007616/ /pubmed/33782451 http://dx.doi.org/10.1038/s41598-021-86367-z Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Bonilla-Quintana, Mayte
Wörgötter, Florentin
Exploring new roles for actin upon LTP induction in dendritic spines
title Exploring new roles for actin upon LTP induction in dendritic spines
title_full Exploring new roles for actin upon LTP induction in dendritic spines
title_fullStr Exploring new roles for actin upon LTP induction in dendritic spines
title_full_unstemmed Exploring new roles for actin upon LTP induction in dendritic spines
title_short Exploring new roles for actin upon LTP induction in dendritic spines
title_sort exploring new roles for actin upon ltp induction in dendritic spines
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8007616/
https://www.ncbi.nlm.nih.gov/pubmed/33782451
http://dx.doi.org/10.1038/s41598-021-86367-z
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