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.
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17 March 2003
Article|
March 17 2003
Formation of filopodia-like bundles in vitro from a dendritic network
Danijela Vignjevic,
Danijela Vignjevic
1Department of Cell and Molecular Biology, Northwestern University Medical School, Chicago, IL 60611
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Defne Yarar,
Defne Yarar
2Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720
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Matthew D. Welch,
Matthew D. Welch
2Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720
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John Peloquin,
John Peloquin
1Department of Cell and Molecular Biology, Northwestern University Medical School, Chicago, IL 60611
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Tatyana Svitkina,
Tatyana Svitkina
1Department of Cell and Molecular Biology, Northwestern University Medical School, Chicago, IL 60611
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Gary G. Borisy
Gary G. Borisy
1Department of Cell and Molecular Biology, Northwestern University Medical School, Chicago, IL 60611
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Danijela Vignjevic
1Department of Cell and Molecular Biology, Northwestern University Medical School, Chicago, IL 60611
Defne Yarar
2Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720
Matthew D. Welch
2Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720
John Peloquin
1Department of Cell and Molecular Biology, Northwestern University Medical School, Chicago, IL 60611
Tatyana Svitkina
1Department of Cell and Molecular Biology, Northwestern University Medical School, Chicago, IL 60611
Gary G. Borisy
1Department of Cell and Molecular Biology, Northwestern University Medical School, Chicago, IL 60611
Address correspondence to Danijela Vignjevic, Northwestern University Medical School, Department of Cell and Molecular Biology, 303 E. Chicago Ave., Ward 8-063, Chicago, IL 60611. Tel.: (312) 503-2854. Fax: (312) 501-7912. E-mail: [email protected]
*
Abbreviations used in this paper: Arp2/3, actin-related protein 2/3; BB, brain buffer; Ena/VASP, enabled/vasodilator-stimulated phosphoprotein; REF, rat embryo fibroblast; VCA, verprolin-homology/connecting/acidic domain of WASP; WASP, Wiskott-Aldrich syndrome protein.
Received:
August 12 2002
Revision Received:
January 24 2003
Accepted:
January 24 2003
Online ISSN: 1540-8140
Print ISSN: 0021-9525
The Rockefeller University Press
2003
J Cell Biol (2003) 160 (6): 951–962.
Article history
Received:
August 12 2002
Revision Received:
January 24 2003
Accepted:
January 24 2003
Citation
Danijela Vignjevic, Defne Yarar, Matthew D. Welch, John Peloquin, Tatyana Svitkina, Gary G. Borisy; Formation of filopodia-like bundles in vitro from a dendritic network . J Cell Biol 17 March 2003; 160 (6): 951–962. doi: https://doi.org/10.1083/jcb.200208059
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