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Fascin-induced actin protrusions are suppressed by dendritic networks in giant unilamellar vesicles
The interactions between actin networks and cell membrane are immensely important for eukaryotic cell functions including cell shape changes, motility, polarity establishment, and adhesion. Actin-binding proteins are known to compete and cooperate using a finite amount of actin monomers to form dist...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8684724/ https://www.ncbi.nlm.nih.gov/pubmed/34133215 http://dx.doi.org/10.1091/mbc.E21-02-0080 |
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author | Wubshet, Nadab H. Bashirzadeh, Yashar Liu, Allen P. |
author_facet | Wubshet, Nadab H. Bashirzadeh, Yashar Liu, Allen P. |
author_sort | Wubshet, Nadab H. |
collection | PubMed |
description | The interactions between actin networks and cell membrane are immensely important for eukaryotic cell functions including cell shape changes, motility, polarity establishment, and adhesion. Actin-binding proteins are known to compete and cooperate using a finite amount of actin monomers to form distinct actin networks. How actin-bundling protein fascin and actin-branching protein Arp2/3 complex compete to remodel membranes is not entirely clear. To investigate fascin- and Arp2/3-mediated actin network remodeling, we applied a reconstitution approach encapsulating bundled and dendritic actin networks inside giant unilamellar vesicles (GUVs). Independently reconstituted, membrane-bound Arp2/3 nucleation forms an actin cortex in GUVs, whereas fascin mediates formation of actin bundles that protrude out of GUVs. Coencapsulating both fascin and Arp2/3 complex leads to polarized dendritic aggregates and significantly reduces membrane protrusions, irrespective of whether the dendritic network is membrane bound or not. However, reducing Arp2/3 complex while increasing fascin restores membrane protrusion. Such changes in network assembly and the subsequent interplay with membrane can be attributed to competition between fascin and Arp2/3 complex to utilize a finite pool of actin. |
format | Online Article Text |
id | pubmed-8684724 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-86847242021-12-20 Fascin-induced actin protrusions are suppressed by dendritic networks in giant unilamellar vesicles Wubshet, Nadab H. Bashirzadeh, Yashar Liu, Allen P. Mol Biol Cell Brief Reports The interactions between actin networks and cell membrane are immensely important for eukaryotic cell functions including cell shape changes, motility, polarity establishment, and adhesion. Actin-binding proteins are known to compete and cooperate using a finite amount of actin monomers to form distinct actin networks. How actin-bundling protein fascin and actin-branching protein Arp2/3 complex compete to remodel membranes is not entirely clear. To investigate fascin- and Arp2/3-mediated actin network remodeling, we applied a reconstitution approach encapsulating bundled and dendritic actin networks inside giant unilamellar vesicles (GUVs). Independently reconstituted, membrane-bound Arp2/3 nucleation forms an actin cortex in GUVs, whereas fascin mediates formation of actin bundles that protrude out of GUVs. Coencapsulating both fascin and Arp2/3 complex leads to polarized dendritic aggregates and significantly reduces membrane protrusions, irrespective of whether the dendritic network is membrane bound or not. However, reducing Arp2/3 complex while increasing fascin restores membrane protrusion. Such changes in network assembly and the subsequent interplay with membrane can be attributed to competition between fascin and Arp2/3 complex to utilize a finite pool of actin. The American Society for Cell Biology 2021-08-19 /pmc/articles/PMC8684724/ /pubmed/34133215 http://dx.doi.org/10.1091/mbc.E21-02-0080 Text en © 2021 Wubshet et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. https://creativecommons.org/licenses/by-nc-sa/3.0/This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License. |
spellingShingle | Brief Reports Wubshet, Nadab H. Bashirzadeh, Yashar Liu, Allen P. Fascin-induced actin protrusions are suppressed by dendritic networks in giant unilamellar vesicles |
title | Fascin-induced actin protrusions are suppressed by dendritic networks in giant unilamellar vesicles |
title_full | Fascin-induced actin protrusions are suppressed by dendritic networks in giant unilamellar vesicles |
title_fullStr | Fascin-induced actin protrusions are suppressed by dendritic networks in giant unilamellar vesicles |
title_full_unstemmed | Fascin-induced actin protrusions are suppressed by dendritic networks in giant unilamellar vesicles |
title_short | Fascin-induced actin protrusions are suppressed by dendritic networks in giant unilamellar vesicles |
title_sort | fascin-induced actin protrusions are suppressed by dendritic networks in giant unilamellar vesicles |
topic | Brief Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8684724/ https://www.ncbi.nlm.nih.gov/pubmed/34133215 http://dx.doi.org/10.1091/mbc.E21-02-0080 |
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