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Neuronal activity remodels the F-actin based submembrane lattice in dendrites but not axons of hippocampal neurons

The nanoscale organization of the F-actin cytoskeleton in neurons comprises membrane-associated periodical rings, bundles, and longitudinal fibers. The F-actin rings have been observed predominantly in axons but only sporadically in dendrites, where fluorescence nanoscopy reveals various patterns of...

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Autores principales: Lavoie-Cardinal, Flavie, Bilodeau, Anthony, Lemieux, Mado, Gardner, Marc-André, Wiesner, Theresa, Laramée, Gabrielle, Gagné, Christian, De Koninck, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7371643/
https://www.ncbi.nlm.nih.gov/pubmed/32686703
http://dx.doi.org/10.1038/s41598-020-68180-2
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author Lavoie-Cardinal, Flavie
Bilodeau, Anthony
Lemieux, Mado
Gardner, Marc-André
Wiesner, Theresa
Laramée, Gabrielle
Gagné, Christian
De Koninck, Paul
author_facet Lavoie-Cardinal, Flavie
Bilodeau, Anthony
Lemieux, Mado
Gardner, Marc-André
Wiesner, Theresa
Laramée, Gabrielle
Gagné, Christian
De Koninck, Paul
author_sort Lavoie-Cardinal, Flavie
collection PubMed
description The nanoscale organization of the F-actin cytoskeleton in neurons comprises membrane-associated periodical rings, bundles, and longitudinal fibers. The F-actin rings have been observed predominantly in axons but only sporadically in dendrites, where fluorescence nanoscopy reveals various patterns of F-actin arranged in mixed patches. These complex dendritic F-actin patterns pose a challenge for investigating quantitatively their regulatory mechanisms. We developed here a weakly supervised deep learning segmentation approach of fluorescence nanoscopy images of F-actin in cultured hippocampal neurons. This approach enabled the quantitative assessment of F-actin remodeling, revealing the disappearance of the rings during neuronal activity in dendrites, but not in axons. The dendritic F-actin cytoskeleton of activated neurons remodeled into longitudinal fibers. We show that this activity-dependent remodeling involves [Formula: see text] and NMDA receptor-dependent mechanisms. This highly dynamic restructuring of dendritic F-actin based submembrane lattice into longitudinal fibers may serve to support activity-dependent membrane remodeling, protein trafficking and neuronal plasticity.
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spelling pubmed-73716432020-07-22 Neuronal activity remodels the F-actin based submembrane lattice in dendrites but not axons of hippocampal neurons Lavoie-Cardinal, Flavie Bilodeau, Anthony Lemieux, Mado Gardner, Marc-André Wiesner, Theresa Laramée, Gabrielle Gagné, Christian De Koninck, Paul Sci Rep Article The nanoscale organization of the F-actin cytoskeleton in neurons comprises membrane-associated periodical rings, bundles, and longitudinal fibers. The F-actin rings have been observed predominantly in axons but only sporadically in dendrites, where fluorescence nanoscopy reveals various patterns of F-actin arranged in mixed patches. These complex dendritic F-actin patterns pose a challenge for investigating quantitatively their regulatory mechanisms. We developed here a weakly supervised deep learning segmentation approach of fluorescence nanoscopy images of F-actin in cultured hippocampal neurons. This approach enabled the quantitative assessment of F-actin remodeling, revealing the disappearance of the rings during neuronal activity in dendrites, but not in axons. The dendritic F-actin cytoskeleton of activated neurons remodeled into longitudinal fibers. We show that this activity-dependent remodeling involves [Formula: see text] and NMDA receptor-dependent mechanisms. This highly dynamic restructuring of dendritic F-actin based submembrane lattice into longitudinal fibers may serve to support activity-dependent membrane remodeling, protein trafficking and neuronal plasticity. Nature Publishing Group UK 2020-07-20 /pmc/articles/PMC7371643/ /pubmed/32686703 http://dx.doi.org/10.1038/s41598-020-68180-2 Text en © The Author(s) 2020 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lavoie-Cardinal, Flavie
Bilodeau, Anthony
Lemieux, Mado
Gardner, Marc-André
Wiesner, Theresa
Laramée, Gabrielle
Gagné, Christian
De Koninck, Paul
Neuronal activity remodels the F-actin based submembrane lattice in dendrites but not axons of hippocampal neurons
title Neuronal activity remodels the F-actin based submembrane lattice in dendrites but not axons of hippocampal neurons
title_full Neuronal activity remodels the F-actin based submembrane lattice in dendrites but not axons of hippocampal neurons
title_fullStr Neuronal activity remodels the F-actin based submembrane lattice in dendrites but not axons of hippocampal neurons
title_full_unstemmed Neuronal activity remodels the F-actin based submembrane lattice in dendrites but not axons of hippocampal neurons
title_short Neuronal activity remodels the F-actin based submembrane lattice in dendrites but not axons of hippocampal neurons
title_sort neuronal activity remodels the f-actin based submembrane lattice in dendrites but not axons of hippocampal neurons
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7371643/
https://www.ncbi.nlm.nih.gov/pubmed/32686703
http://dx.doi.org/10.1038/s41598-020-68180-2
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