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Discrete mechanical model of lamellipodial actin network implements molecular clutch mechanism and generates arcs and microspikes

Mechanical forces, actin filament turnover, and adhesion to the extracellular environment regulate lamellipodial protrusions. Computational and mathematical models at the continuum level have been used to investigate the molecular clutch mechanism, calculating the stress profile through the lamellip...

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Autores principales: Rutkowski, David M., Vavylonis, Dimitrios
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8553091/
https://www.ncbi.nlm.nih.gov/pubmed/34662335
http://dx.doi.org/10.1371/journal.pcbi.1009506
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author Rutkowski, David M.
Vavylonis, Dimitrios
author_facet Rutkowski, David M.
Vavylonis, Dimitrios
author_sort Rutkowski, David M.
collection PubMed
description Mechanical forces, actin filament turnover, and adhesion to the extracellular environment regulate lamellipodial protrusions. Computational and mathematical models at the continuum level have been used to investigate the molecular clutch mechanism, calculating the stress profile through the lamellipodium and around focal adhesions. However, the forces and deformations of individual actin filaments have not been considered while interactions between actin networks and actin bundles is not easily accounted with such methods. We develop a filament-level model of a lamellipodial actin network undergoing retrograde flow using 3D Brownian dynamics. Retrograde flow is promoted in simulations by pushing forces from the leading edge (due to actin polymerization), pulling forces (due to molecular motors), and opposed by viscous drag in cytoplasm and focal adhesions. Simulated networks have densities similar to measurements in prior electron micrographs. Connectivity between individual actin segments is maintained by permanent and dynamic crosslinkers. Remodeling of the network occurs via the addition of single actin filaments near the leading edge and via filament bond severing. We investigated how several parameters affect the stress distribution, network deformation and retrograde flow speed. The model captures the decrease in retrograde flow upon increase of focal adhesion strength. The stress profile changes from compression to extension across the leading edge, with regions of filament bending around focal adhesions. The model reproduces the observed reduction in retrograde flow speed upon exposure to cytochalasin D, which halts actin polymerization. Changes in crosslinker concentration and dynamics, as well as in the orientation pattern of newly added filaments demonstrate the model’s ability to generate bundles of filaments perpendicular (actin arcs) or parallel (microspikes) to the protruding direction.
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spelling pubmed-85530912021-10-29 Discrete mechanical model of lamellipodial actin network implements molecular clutch mechanism and generates arcs and microspikes Rutkowski, David M. Vavylonis, Dimitrios PLoS Comput Biol Research Article Mechanical forces, actin filament turnover, and adhesion to the extracellular environment regulate lamellipodial protrusions. Computational and mathematical models at the continuum level have been used to investigate the molecular clutch mechanism, calculating the stress profile through the lamellipodium and around focal adhesions. However, the forces and deformations of individual actin filaments have not been considered while interactions between actin networks and actin bundles is not easily accounted with such methods. We develop a filament-level model of a lamellipodial actin network undergoing retrograde flow using 3D Brownian dynamics. Retrograde flow is promoted in simulations by pushing forces from the leading edge (due to actin polymerization), pulling forces (due to molecular motors), and opposed by viscous drag in cytoplasm and focal adhesions. Simulated networks have densities similar to measurements in prior electron micrographs. Connectivity between individual actin segments is maintained by permanent and dynamic crosslinkers. Remodeling of the network occurs via the addition of single actin filaments near the leading edge and via filament bond severing. We investigated how several parameters affect the stress distribution, network deformation and retrograde flow speed. The model captures the decrease in retrograde flow upon increase of focal adhesion strength. The stress profile changes from compression to extension across the leading edge, with regions of filament bending around focal adhesions. The model reproduces the observed reduction in retrograde flow speed upon exposure to cytochalasin D, which halts actin polymerization. Changes in crosslinker concentration and dynamics, as well as in the orientation pattern of newly added filaments demonstrate the model’s ability to generate bundles of filaments perpendicular (actin arcs) or parallel (microspikes) to the protruding direction. Public Library of Science 2021-10-18 /pmc/articles/PMC8553091/ /pubmed/34662335 http://dx.doi.org/10.1371/journal.pcbi.1009506 Text en © 2021 Rutkowski, Vavylonis https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Rutkowski, David M.
Vavylonis, Dimitrios
Discrete mechanical model of lamellipodial actin network implements molecular clutch mechanism and generates arcs and microspikes
title Discrete mechanical model of lamellipodial actin network implements molecular clutch mechanism and generates arcs and microspikes
title_full Discrete mechanical model of lamellipodial actin network implements molecular clutch mechanism and generates arcs and microspikes
title_fullStr Discrete mechanical model of lamellipodial actin network implements molecular clutch mechanism and generates arcs and microspikes
title_full_unstemmed Discrete mechanical model of lamellipodial actin network implements molecular clutch mechanism and generates arcs and microspikes
title_short Discrete mechanical model of lamellipodial actin network implements molecular clutch mechanism and generates arcs and microspikes
title_sort discrete mechanical model of lamellipodial actin network implements molecular clutch mechanism and generates arcs and microspikes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8553091/
https://www.ncbi.nlm.nih.gov/pubmed/34662335
http://dx.doi.org/10.1371/journal.pcbi.1009506
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