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Actin dynamics in cell migration

Cell migration is an essential process, both in unicellular organisms such as amoeba and as individual or collective motility in highly developed multicellular organisms like mammals. It is controlled by a variety of activities combining protrusive and contractile forces, normally generated by actin...

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Autores principales: Schaks, Matthias, Giannone, Grégory, Rottner, Klemens
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6823167/
https://www.ncbi.nlm.nih.gov/pubmed/31551324
http://dx.doi.org/10.1042/EBC20190015
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author Schaks, Matthias
Giannone, Grégory
Rottner, Klemens
author_facet Schaks, Matthias
Giannone, Grégory
Rottner, Klemens
author_sort Schaks, Matthias
collection PubMed
description Cell migration is an essential process, both in unicellular organisms such as amoeba and as individual or collective motility in highly developed multicellular organisms like mammals. It is controlled by a variety of activities combining protrusive and contractile forces, normally generated by actin filaments. Here, we summarize actin filament assembly and turnover processes, and how respective biochemical activities translate into different protrusion types engaged in migration. These actin-based plasma membrane protrusions include actin-related protein 2/3 complex-dependent structures such as lamellipodia and membrane ruffles, filopodia as well as plasma membrane blebs. We also address observed antagonisms between these protrusion types, and propose a model – also inspired by previous literature – in which a complex balance between specific Rho GTPase signaling pathways dictates the protrusion mechanism employed by cells. Furthermore, we revisit published work regarding the fascinating antagonism between Rac and Rho GTPases, and how this intricate signaling network can define cell behavior and modes of migration. Finally, we discuss how the assembly of actin filament networks can feed back onto their regulators, as exemplified for the lamellipodial factor WAVE regulatory complex, tightly controlling accumulation of this complex at specific subcellular locations as well as its turnover.
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spelling pubmed-68231672019-11-12 Actin dynamics in cell migration Schaks, Matthias Giannone, Grégory Rottner, Klemens Essays Biochem Molecular Interactions Cell migration is an essential process, both in unicellular organisms such as amoeba and as individual or collective motility in highly developed multicellular organisms like mammals. It is controlled by a variety of activities combining protrusive and contractile forces, normally generated by actin filaments. Here, we summarize actin filament assembly and turnover processes, and how respective biochemical activities translate into different protrusion types engaged in migration. These actin-based plasma membrane protrusions include actin-related protein 2/3 complex-dependent structures such as lamellipodia and membrane ruffles, filopodia as well as plasma membrane blebs. We also address observed antagonisms between these protrusion types, and propose a model – also inspired by previous literature – in which a complex balance between specific Rho GTPase signaling pathways dictates the protrusion mechanism employed by cells. Furthermore, we revisit published work regarding the fascinating antagonism between Rac and Rho GTPases, and how this intricate signaling network can define cell behavior and modes of migration. Finally, we discuss how the assembly of actin filament networks can feed back onto their regulators, as exemplified for the lamellipodial factor WAVE regulatory complex, tightly controlling accumulation of this complex at specific subcellular locations as well as its turnover. Portland Press Ltd. 2019-10 2019-09-24 /pmc/articles/PMC6823167/ /pubmed/31551324 http://dx.doi.org/10.1042/EBC20190015 Text en © 2019 The Author(s). https://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY-NC-ND).
spellingShingle Molecular Interactions
Schaks, Matthias
Giannone, Grégory
Rottner, Klemens
Actin dynamics in cell migration
title Actin dynamics in cell migration
title_full Actin dynamics in cell migration
title_fullStr Actin dynamics in cell migration
title_full_unstemmed Actin dynamics in cell migration
title_short Actin dynamics in cell migration
title_sort actin dynamics in cell migration
topic Molecular Interactions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6823167/
https://www.ncbi.nlm.nih.gov/pubmed/31551324
http://dx.doi.org/10.1042/EBC20190015
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