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Arp2/3 complex inhibition radically alters lamellipodial actin architecture, suspended cell shape, and the cell spreading process

Recent studies have investigated the dendritic actin cytoskeleton of the cell edge's lamellipodial (LP) region by experimentally decreasing the activity of the actin filament nucleator and branch former, the Arp2/3 complex. Here we extend these studies via pharmacological inhibition of the Arp2...

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Autores principales: Henson, John H., Yeterian, Mesrob, Weeks, Richard M., Medrano, Angela E., Brown, Briana L., Geist, Heather L., Pais, Mollyann D., Oldenbourg, Rudolf, Shuster, Charles B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4342025/
https://www.ncbi.nlm.nih.gov/pubmed/25568343
http://dx.doi.org/10.1091/mbc.E14-07-1244
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author Henson, John H.
Yeterian, Mesrob
Weeks, Richard M.
Medrano, Angela E.
Brown, Briana L.
Geist, Heather L.
Pais, Mollyann D.
Oldenbourg, Rudolf
Shuster, Charles B.
author_facet Henson, John H.
Yeterian, Mesrob
Weeks, Richard M.
Medrano, Angela E.
Brown, Briana L.
Geist, Heather L.
Pais, Mollyann D.
Oldenbourg, Rudolf
Shuster, Charles B.
author_sort Henson, John H.
collection PubMed
description Recent studies have investigated the dendritic actin cytoskeleton of the cell edge's lamellipodial (LP) region by experimentally decreasing the activity of the actin filament nucleator and branch former, the Arp2/3 complex. Here we extend these studies via pharmacological inhibition of the Arp2/3 complex in sea urchin coelomocytes, cells that possess an unusually broad LP region and display correspondingly exaggerated centripetal flow. Using light and electron microscopy, we demonstrate that Arp2/3 complex inhibition via the drug CK666 dramatically altered LP actin architecture, slowed centripetal flow, drove a lamellipodial-to-filopodial shape change in suspended cells, and induced a novel actin structural organization during cell spreading. A general feature of the CK666 phenotype in coelomocytes was transverse actin arcs, and arc generation was arrested by a formin inhibitor. We also demonstrate that CK666 treatment produces actin arcs in other cells with broad LP regions, namely fish keratocytes and Drosophila S2 cells. We hypothesize that the actin arcs made visible by Arp2/3 complex inhibition in coelomocytes may represent an exaggerated manifestation of the elongate mother filaments that could possibly serve as the scaffold for the production of the dendritic actin network.
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spelling pubmed-43420252015-05-16 Arp2/3 complex inhibition radically alters lamellipodial actin architecture, suspended cell shape, and the cell spreading process Henson, John H. Yeterian, Mesrob Weeks, Richard M. Medrano, Angela E. Brown, Briana L. Geist, Heather L. Pais, Mollyann D. Oldenbourg, Rudolf Shuster, Charles B. Mol Biol Cell Articles Recent studies have investigated the dendritic actin cytoskeleton of the cell edge's lamellipodial (LP) region by experimentally decreasing the activity of the actin filament nucleator and branch former, the Arp2/3 complex. Here we extend these studies via pharmacological inhibition of the Arp2/3 complex in sea urchin coelomocytes, cells that possess an unusually broad LP region and display correspondingly exaggerated centripetal flow. Using light and electron microscopy, we demonstrate that Arp2/3 complex inhibition via the drug CK666 dramatically altered LP actin architecture, slowed centripetal flow, drove a lamellipodial-to-filopodial shape change in suspended cells, and induced a novel actin structural organization during cell spreading. A general feature of the CK666 phenotype in coelomocytes was transverse actin arcs, and arc generation was arrested by a formin inhibitor. We also demonstrate that CK666 treatment produces actin arcs in other cells with broad LP regions, namely fish keratocytes and Drosophila S2 cells. We hypothesize that the actin arcs made visible by Arp2/3 complex inhibition in coelomocytes may represent an exaggerated manifestation of the elongate mother filaments that could possibly serve as the scaffold for the production of the dendritic actin network. The American Society for Cell Biology 2015-03-01 /pmc/articles/PMC4342025/ /pubmed/25568343 http://dx.doi.org/10.1091/mbc.E14-07-1244 Text en © 2015 Henson et al. 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 (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology.
spellingShingle Articles
Henson, John H.
Yeterian, Mesrob
Weeks, Richard M.
Medrano, Angela E.
Brown, Briana L.
Geist, Heather L.
Pais, Mollyann D.
Oldenbourg, Rudolf
Shuster, Charles B.
Arp2/3 complex inhibition radically alters lamellipodial actin architecture, suspended cell shape, and the cell spreading process
title Arp2/3 complex inhibition radically alters lamellipodial actin architecture, suspended cell shape, and the cell spreading process
title_full Arp2/3 complex inhibition radically alters lamellipodial actin architecture, suspended cell shape, and the cell spreading process
title_fullStr Arp2/3 complex inhibition radically alters lamellipodial actin architecture, suspended cell shape, and the cell spreading process
title_full_unstemmed Arp2/3 complex inhibition radically alters lamellipodial actin architecture, suspended cell shape, and the cell spreading process
title_short Arp2/3 complex inhibition radically alters lamellipodial actin architecture, suspended cell shape, and the cell spreading process
title_sort arp2/3 complex inhibition radically alters lamellipodial actin architecture, suspended cell shape, and the cell spreading process
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4342025/
https://www.ncbi.nlm.nih.gov/pubmed/25568343
http://dx.doi.org/10.1091/mbc.E14-07-1244
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