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Filopodia rotate and coil by actively generating twist in their actin shaft

Filopodia are actin-rich structures, present on the surface of eukaryotic cells. These structures play a pivotal role by allowing cells to explore their environment, generate mechanical forces or perform chemical signaling. Their complex dynamics includes buckling, pulling, length and shape changes....

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Autores principales: Leijnse, Natascha, Barooji, Younes Farhangi, Arastoo, Mohammad Reza, Sønder, Stine Lauritzen, Verhagen, Bram, Wullkopf, Lena, Erler, Janine Terra, Semsey, Szabolcs, Nylandsted, Jesper, Oddershede, Lene Broeng, Doostmohammadi, Amin, Bendix, Poul Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8960877/
https://www.ncbi.nlm.nih.gov/pubmed/35347113
http://dx.doi.org/10.1038/s41467-022-28961-x
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author Leijnse, Natascha
Barooji, Younes Farhangi
Arastoo, Mohammad Reza
Sønder, Stine Lauritzen
Verhagen, Bram
Wullkopf, Lena
Erler, Janine Terra
Semsey, Szabolcs
Nylandsted, Jesper
Oddershede, Lene Broeng
Doostmohammadi, Amin
Bendix, Poul Martin
author_facet Leijnse, Natascha
Barooji, Younes Farhangi
Arastoo, Mohammad Reza
Sønder, Stine Lauritzen
Verhagen, Bram
Wullkopf, Lena
Erler, Janine Terra
Semsey, Szabolcs
Nylandsted, Jesper
Oddershede, Lene Broeng
Doostmohammadi, Amin
Bendix, Poul Martin
author_sort Leijnse, Natascha
collection PubMed
description Filopodia are actin-rich structures, present on the surface of eukaryotic cells. These structures play a pivotal role by allowing cells to explore their environment, generate mechanical forces or perform chemical signaling. Their complex dynamics includes buckling, pulling, length and shape changes. We show that filopodia additionally explore their 3D extracellular space by combining growth and shrinking with axial twisting and buckling. Importantly, the actin core inside filopodia performs a twisting or spinning motion which is observed for a range of cell types spanning from earliest development to highly differentiated tissue cells. Non-equilibrium physical modeling of actin and myosin confirm that twist is an emergent phenomenon of active filaments confined in a narrow channel which is supported by measured traction forces and helical buckles that can be ascribed to accumulation of sufficient twist. These results lead us to conclude that activity induced twisting of the actin shaft is a general mechanism underlying fundamental functions of filopodia.
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spelling pubmed-89608772022-04-20 Filopodia rotate and coil by actively generating twist in their actin shaft Leijnse, Natascha Barooji, Younes Farhangi Arastoo, Mohammad Reza Sønder, Stine Lauritzen Verhagen, Bram Wullkopf, Lena Erler, Janine Terra Semsey, Szabolcs Nylandsted, Jesper Oddershede, Lene Broeng Doostmohammadi, Amin Bendix, Poul Martin Nat Commun Article Filopodia are actin-rich structures, present on the surface of eukaryotic cells. These structures play a pivotal role by allowing cells to explore their environment, generate mechanical forces or perform chemical signaling. Their complex dynamics includes buckling, pulling, length and shape changes. We show that filopodia additionally explore their 3D extracellular space by combining growth and shrinking with axial twisting and buckling. Importantly, the actin core inside filopodia performs a twisting or spinning motion which is observed for a range of cell types spanning from earliest development to highly differentiated tissue cells. Non-equilibrium physical modeling of actin and myosin confirm that twist is an emergent phenomenon of active filaments confined in a narrow channel which is supported by measured traction forces and helical buckles that can be ascribed to accumulation of sufficient twist. These results lead us to conclude that activity induced twisting of the actin shaft is a general mechanism underlying fundamental functions of filopodia. Nature Publishing Group UK 2022-03-28 /pmc/articles/PMC8960877/ /pubmed/35347113 http://dx.doi.org/10.1038/s41467-022-28961-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Leijnse, Natascha
Barooji, Younes Farhangi
Arastoo, Mohammad Reza
Sønder, Stine Lauritzen
Verhagen, Bram
Wullkopf, Lena
Erler, Janine Terra
Semsey, Szabolcs
Nylandsted, Jesper
Oddershede, Lene Broeng
Doostmohammadi, Amin
Bendix, Poul Martin
Filopodia rotate and coil by actively generating twist in their actin shaft
title Filopodia rotate and coil by actively generating twist in their actin shaft
title_full Filopodia rotate and coil by actively generating twist in their actin shaft
title_fullStr Filopodia rotate and coil by actively generating twist in their actin shaft
title_full_unstemmed Filopodia rotate and coil by actively generating twist in their actin shaft
title_short Filopodia rotate and coil by actively generating twist in their actin shaft
title_sort filopodia rotate and coil by actively generating twist in their actin shaft
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8960877/
https://www.ncbi.nlm.nih.gov/pubmed/35347113
http://dx.doi.org/10.1038/s41467-022-28961-x
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