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The cell pushes back: The Arp2/3 complex is a key orchestrator of cellular responses to environmental forces
The Arp2/3 complex orchestrates the formation of branched actin networks at the interface between the cytoplasm and membranes. Although it is widely appreciated that these networks are useful for scaffolding, creating pushing forces and delineating zones at the membrane interface, it has only recent...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7938217/ https://www.ncbi.nlm.nih.gov/pubmed/32977244 http://dx.doi.org/10.1016/j.ceb.2020.08.012 |
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author | Papalazarou, Vassilis Machesky, Laura M. |
author_facet | Papalazarou, Vassilis Machesky, Laura M. |
author_sort | Papalazarou, Vassilis |
collection | PubMed |
description | The Arp2/3 complex orchestrates the formation of branched actin networks at the interface between the cytoplasm and membranes. Although it is widely appreciated that these networks are useful for scaffolding, creating pushing forces and delineating zones at the membrane interface, it has only recently come to light that branched actin networks are mechanosensitive, giving them special properties. Here, we discuss recent advances in our understanding of how Arp2/3-generated actin networks respond to load forces and thus allow cells to create pushing forces in responsive and tuneable ways to effect cellular processes such as migration, invasion, phagocytosis, adhesion and even nuclear and DNA damage repair. |
format | Online Article Text |
id | pubmed-7938217 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-79382172021-03-16 The cell pushes back: The Arp2/3 complex is a key orchestrator of cellular responses to environmental forces Papalazarou, Vassilis Machesky, Laura M. Curr Opin Cell Biol Article The Arp2/3 complex orchestrates the formation of branched actin networks at the interface between the cytoplasm and membranes. Although it is widely appreciated that these networks are useful for scaffolding, creating pushing forces and delineating zones at the membrane interface, it has only recently come to light that branched actin networks are mechanosensitive, giving them special properties. Here, we discuss recent advances in our understanding of how Arp2/3-generated actin networks respond to load forces and thus allow cells to create pushing forces in responsive and tuneable ways to effect cellular processes such as migration, invasion, phagocytosis, adhesion and even nuclear and DNA damage repair. Elsevier 2021-02 /pmc/articles/PMC7938217/ /pubmed/32977244 http://dx.doi.org/10.1016/j.ceb.2020.08.012 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Papalazarou, Vassilis Machesky, Laura M. The cell pushes back: The Arp2/3 complex is a key orchestrator of cellular responses to environmental forces |
title | The cell pushes back: The Arp2/3 complex is a key orchestrator of cellular responses to environmental forces |
title_full | The cell pushes back: The Arp2/3 complex is a key orchestrator of cellular responses to environmental forces |
title_fullStr | The cell pushes back: The Arp2/3 complex is a key orchestrator of cellular responses to environmental forces |
title_full_unstemmed | The cell pushes back: The Arp2/3 complex is a key orchestrator of cellular responses to environmental forces |
title_short | The cell pushes back: The Arp2/3 complex is a key orchestrator of cellular responses to environmental forces |
title_sort | cell pushes back: the arp2/3 complex is a key orchestrator of cellular responses to environmental forces |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7938217/ https://www.ncbi.nlm.nih.gov/pubmed/32977244 http://dx.doi.org/10.1016/j.ceb.2020.08.012 |
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