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Influence of cross-linking and retrograde flow on formation and dynamics of lamellipodium

The forces that arise from the actin cortex play a crucial role in determining the membrane deformation. These include protrusive forces due to actin polymerization, pulling forces due to transient attachment of actin filaments to the membrane, retrograde flow powered by contraction of actomyosin ne...

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Detalles Bibliográficos
Autores principales: Atakhani, Asal, Mohammad-Rafiee, Farshid, Gholami, Azam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6428246/
https://www.ncbi.nlm.nih.gov/pubmed/30897104
http://dx.doi.org/10.1371/journal.pone.0213810
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author Atakhani, Asal
Mohammad-Rafiee, Farshid
Gholami, Azam
author_facet Atakhani, Asal
Mohammad-Rafiee, Farshid
Gholami, Azam
author_sort Atakhani, Asal
collection PubMed
description The forces that arise from the actin cortex play a crucial role in determining the membrane deformation. These include protrusive forces due to actin polymerization, pulling forces due to transient attachment of actin filaments to the membrane, retrograde flow powered by contraction of actomyosin network, and adhesion to the extracellular matrix. Here we present a theoretical model for membrane deformation resulting from the feedback between the membrane shape and the forces acting on the membrane. We model the membrane as a series of beads connected by springs and determine the final steady-state shape of the membrane arising from the interplay between pushing/pulling forces of the actin network and the resisting membrane tension. We specifically investigate the effect of the gel dynamics on the spatio-temporal deformation of the membrane until a stable lamellipodium is formed. We show that the retrograde flow and the cross-linking velocity play an essential role in the final elongation of the membrane. Interestingly, in the simulations where motor-induced contractility is switched off, reduced retrograde flow results in an increase in the rate and amplitude of membrane protrusion. These simulations are consistent with experimental observations that report an enhancement in protrusion efficiency as myosin II molecular motors are inhibited.
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spelling pubmed-64282462019-04-02 Influence of cross-linking and retrograde flow on formation and dynamics of lamellipodium Atakhani, Asal Mohammad-Rafiee, Farshid Gholami, Azam PLoS One Research Article The forces that arise from the actin cortex play a crucial role in determining the membrane deformation. These include protrusive forces due to actin polymerization, pulling forces due to transient attachment of actin filaments to the membrane, retrograde flow powered by contraction of actomyosin network, and adhesion to the extracellular matrix. Here we present a theoretical model for membrane deformation resulting from the feedback between the membrane shape and the forces acting on the membrane. We model the membrane as a series of beads connected by springs and determine the final steady-state shape of the membrane arising from the interplay between pushing/pulling forces of the actin network and the resisting membrane tension. We specifically investigate the effect of the gel dynamics on the spatio-temporal deformation of the membrane until a stable lamellipodium is formed. We show that the retrograde flow and the cross-linking velocity play an essential role in the final elongation of the membrane. Interestingly, in the simulations where motor-induced contractility is switched off, reduced retrograde flow results in an increase in the rate and amplitude of membrane protrusion. These simulations are consistent with experimental observations that report an enhancement in protrusion efficiency as myosin II molecular motors are inhibited. Public Library of Science 2019-03-21 /pmc/articles/PMC6428246/ /pubmed/30897104 http://dx.doi.org/10.1371/journal.pone.0213810 Text en © 2019 Atakhani et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://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
Atakhani, Asal
Mohammad-Rafiee, Farshid
Gholami, Azam
Influence of cross-linking and retrograde flow on formation and dynamics of lamellipodium
title Influence of cross-linking and retrograde flow on formation and dynamics of lamellipodium
title_full Influence of cross-linking and retrograde flow on formation and dynamics of lamellipodium
title_fullStr Influence of cross-linking and retrograde flow on formation and dynamics of lamellipodium
title_full_unstemmed Influence of cross-linking and retrograde flow on formation and dynamics of lamellipodium
title_short Influence of cross-linking and retrograde flow on formation and dynamics of lamellipodium
title_sort influence of cross-linking and retrograde flow on formation and dynamics of lamellipodium
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6428246/
https://www.ncbi.nlm.nih.gov/pubmed/30897104
http://dx.doi.org/10.1371/journal.pone.0213810
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