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A network of mixed actin polarity in the leading edge of spreading cells

Physical interactions of cells with the underlying extracellular matrix (ECM) play key roles in multiple cellular processes. The actin cytoskeleton is a central driver and regulator of cellular dynamics, that produces membrane-protrusions such as lamellipodia and filopodia. Here, we examined actin o...

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Autores principales: Chung, Wen-Lu, Eibauer, Matthias, Li, Wenhong, Boujemaa-Paterski, Rajaa, Geiger, Benjamin, Medalia, Ohad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9727120/
https://www.ncbi.nlm.nih.gov/pubmed/36473943
http://dx.doi.org/10.1038/s42003-022-04288-7
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author Chung, Wen-Lu
Eibauer, Matthias
Li, Wenhong
Boujemaa-Paterski, Rajaa
Geiger, Benjamin
Medalia, Ohad
author_facet Chung, Wen-Lu
Eibauer, Matthias
Li, Wenhong
Boujemaa-Paterski, Rajaa
Geiger, Benjamin
Medalia, Ohad
author_sort Chung, Wen-Lu
collection PubMed
description Physical interactions of cells with the underlying extracellular matrix (ECM) play key roles in multiple cellular processes. The actin cytoskeleton is a central driver and regulator of cellular dynamics, that produces membrane-protrusions such as lamellipodia and filopodia. Here, we examined actin organization in expanding lamellipodia during early stages of cell spreading. To gain insight into the 3D actin organization, we plated fibroblasts on galectin-8 coated EM grids, an ECM protein presents in disease states. We then combined cryo-electron tomography with advanced image processing tools for reconstructing the structure of F-actin in the lamellipodia. This approach enabled us to resolve the polarity and orientation of filaments, and the structure of the Arp2/3 complexes associated with F-actin branches. We show that F-actin in lamellipodial protrusions forms a dense network with three distinct sub-domains. One consists primarily of radial filaments, with their barbed ends pointing towards the membrane, the other is enriched with parallel filaments that run between the radial fibers, in addition to an intermediate sub-domain. Surprisingly, a minor, yet significant (~10%) population of actin filaments, are oriented with their barbed-ends towards the cell center. Our results provide structural insights into F-actin assembly and dynamic reorganization in the leading edge of spreading cells.
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spelling pubmed-97271202022-12-08 A network of mixed actin polarity in the leading edge of spreading cells Chung, Wen-Lu Eibauer, Matthias Li, Wenhong Boujemaa-Paterski, Rajaa Geiger, Benjamin Medalia, Ohad Commun Biol Article Physical interactions of cells with the underlying extracellular matrix (ECM) play key roles in multiple cellular processes. The actin cytoskeleton is a central driver and regulator of cellular dynamics, that produces membrane-protrusions such as lamellipodia and filopodia. Here, we examined actin organization in expanding lamellipodia during early stages of cell spreading. To gain insight into the 3D actin organization, we plated fibroblasts on galectin-8 coated EM grids, an ECM protein presents in disease states. We then combined cryo-electron tomography with advanced image processing tools for reconstructing the structure of F-actin in the lamellipodia. This approach enabled us to resolve the polarity and orientation of filaments, and the structure of the Arp2/3 complexes associated with F-actin branches. We show that F-actin in lamellipodial protrusions forms a dense network with three distinct sub-domains. One consists primarily of radial filaments, with their barbed ends pointing towards the membrane, the other is enriched with parallel filaments that run between the radial fibers, in addition to an intermediate sub-domain. Surprisingly, a minor, yet significant (~10%) population of actin filaments, are oriented with their barbed-ends towards the cell center. Our results provide structural insights into F-actin assembly and dynamic reorganization in the leading edge of spreading cells. Nature Publishing Group UK 2022-12-07 /pmc/articles/PMC9727120/ /pubmed/36473943 http://dx.doi.org/10.1038/s42003-022-04288-7 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
Chung, Wen-Lu
Eibauer, Matthias
Li, Wenhong
Boujemaa-Paterski, Rajaa
Geiger, Benjamin
Medalia, Ohad
A network of mixed actin polarity in the leading edge of spreading cells
title A network of mixed actin polarity in the leading edge of spreading cells
title_full A network of mixed actin polarity in the leading edge of spreading cells
title_fullStr A network of mixed actin polarity in the leading edge of spreading cells
title_full_unstemmed A network of mixed actin polarity in the leading edge of spreading cells
title_short A network of mixed actin polarity in the leading edge of spreading cells
title_sort network of mixed actin polarity in the leading edge of spreading cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9727120/
https://www.ncbi.nlm.nih.gov/pubmed/36473943
http://dx.doi.org/10.1038/s42003-022-04288-7
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