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dc.contributor.authorHenson, John H.  Concept link
dc.contributor.authorYeterian, Mesrob  Concept link
dc.contributor.authorWeeks, Richard M.  Concept link
dc.contributor.authorMedrano, Angela E.  Concept link
dc.contributor.authorBrown, Briana L.  Concept link
dc.contributor.authorGeist, Heather L.  Concept link
dc.contributor.authorPais, Mollyann D.  Concept link
dc.contributor.authorOldenbourg, Rudolf  Concept link
dc.contributor.authorShuster, Charles B.  Concept link
dc.identifier.citationMolecular Biology of the Cell 26 (2015): 887-900en_US
dc.description© The Author(s), 2015. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Molecular Biology of the Cell 26 (2015): 887-900, doi:10.1091/mbc.E14-07-1244.en_US
dc.description.abstractRecent 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.en_US
dc.description.sponsorshipThis research was supported by National Science Foundation STEP grant 0856704 to Dickinson College, student/faculty summer research grants from the Dickinson College Research and Development Committee, Laura and Arthur Colwin Summer Research Fellowships from the Marine Biological Laboratory to J.H.H. and C.B.S., National Institutes of Health Grant EB002583 to R.O., and National Science Foundation collaborative research grants to J.H.H. (MCB-1412688) and C.B.S. (MCB-1412734).en_US
dc.publisherAmerican Society for Cell Biologyen_US
dc.rightsAttribution-NonCommercial-ShareAlike 3.0 Unported*
dc.titleArp2/3 complex inhibition radically alters lamellipodial actin architecture, suspended cell shape, and the cell spreading processen_US

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