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Formation of filopodia-like bundles in vitro from a dendritic network
We report the development and characterization of an in vitro system for the formation of filopodia-like bundles. Beads coated with actin-related protein 2/3 (Arp2/3)–activating proteins can induce two distinct types of actin organization in cytoplasmic extracts: (1) comet tails or clouds displaying...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2003
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2173766/ https://www.ncbi.nlm.nih.gov/pubmed/12642617 http://dx.doi.org/10.1083/jcb.200208059 |
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author | Vignjevic, Danijela Yarar, Defne Welch, Matthew D. Peloquin, John Svitkina, Tatyana Borisy, Gary G. |
author_facet | Vignjevic, Danijela Yarar, Defne Welch, Matthew D. Peloquin, John Svitkina, Tatyana Borisy, Gary G. |
author_sort | Vignjevic, Danijela |
collection | PubMed |
description | We report the development and characterization of an in vitro system for the formation of filopodia-like bundles. Beads coated with actin-related protein 2/3 (Arp2/3)–activating proteins can induce two distinct types of actin organization in cytoplasmic extracts: (1) comet tails or clouds displaying a dendritic array of actin filaments and (2) stars with filament bundles radiating from the bead. Actin filaments in these bundles, like those in filopodia, are long, unbranched, aligned, uniformly polar, and grow at the barbed end. Like filopodia, star bundles are enriched in fascin and lack Arp2/3 complex and capping protein. Transition from dendritic to bundled organization was induced by depletion of capping protein, and add-back of this protein restored the dendritic mode. Depletion experiments demonstrated that star formation is dependent on Arp2/3 complex. This poses the paradox of how Arp2/3 complex can be involved in the formation of both branched (lamellipodia-like) and unbranched (filopodia-like) actin structures. Using purified proteins, we showed that a small number of components are sufficient for the assembly of filopodia-like bundles: Wiskott-Aldrich syndrome protein (WASP)–coated beads, actin, Arp2/3 complex, and fascin. We propose a model for filopodial formation in which actin filaments of a preexisting dendritic network are elongated by inhibition of capping and subsequently cross-linked into bundles by fascin. |
format | Text |
id | pubmed-2173766 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21737662008-05-01 Formation of filopodia-like bundles in vitro from a dendritic network Vignjevic, Danijela Yarar, Defne Welch, Matthew D. Peloquin, John Svitkina, Tatyana Borisy, Gary G. J Cell Biol Article We report the development and characterization of an in vitro system for the formation of filopodia-like bundles. Beads coated with actin-related protein 2/3 (Arp2/3)–activating proteins can induce two distinct types of actin organization in cytoplasmic extracts: (1) comet tails or clouds displaying a dendritic array of actin filaments and (2) stars with filament bundles radiating from the bead. Actin filaments in these bundles, like those in filopodia, are long, unbranched, aligned, uniformly polar, and grow at the barbed end. Like filopodia, star bundles are enriched in fascin and lack Arp2/3 complex and capping protein. Transition from dendritic to bundled organization was induced by depletion of capping protein, and add-back of this protein restored the dendritic mode. Depletion experiments demonstrated that star formation is dependent on Arp2/3 complex. This poses the paradox of how Arp2/3 complex can be involved in the formation of both branched (lamellipodia-like) and unbranched (filopodia-like) actin structures. Using purified proteins, we showed that a small number of components are sufficient for the assembly of filopodia-like bundles: Wiskott-Aldrich syndrome protein (WASP)–coated beads, actin, Arp2/3 complex, and fascin. We propose a model for filopodial formation in which actin filaments of a preexisting dendritic network are elongated by inhibition of capping and subsequently cross-linked into bundles by fascin. The Rockefeller University Press 2003-03-17 /pmc/articles/PMC2173766/ /pubmed/12642617 http://dx.doi.org/10.1083/jcb.200208059 Text en Copyright © 2003, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Article Vignjevic, Danijela Yarar, Defne Welch, Matthew D. Peloquin, John Svitkina, Tatyana Borisy, Gary G. Formation of filopodia-like bundles in vitro from a dendritic network |
title | Formation of filopodia-like bundles in vitro from a dendritic network |
title_full | Formation of filopodia-like bundles in vitro from a dendritic network |
title_fullStr | Formation of filopodia-like bundles in vitro from a dendritic network |
title_full_unstemmed | Formation of filopodia-like bundles in vitro from a dendritic network |
title_short | Formation of filopodia-like bundles in vitro from a dendritic network |
title_sort | formation of filopodia-like bundles in vitro from a dendritic network |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2173766/ https://www.ncbi.nlm.nih.gov/pubmed/12642617 http://dx.doi.org/10.1083/jcb.200208059 |
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