Direct observation of dendritic actin filament networks nucleated by Arp2/3 complex and WASP/Scar proteins
Abstract
Most nucleated cells crawl about by extending a pseudopod that is driven by the polymerization of actin filaments in the cytoplasm behind the leading edge of the plasma membrane. These actin filaments are linked into a network by Y-branches, with the pointed end of each filament attached to the side of another filament and the rapidly growing barbed end facing forward. Because Arp2/3 complex nucleates actin polymerization and links the pointed end to the side of another filament in vitro, a dendritic nucleation model has been proposed in which Arp2/3 complex initiates filaments from the sides of older filaments. Here we report, by using a light microscopy assay, many new features of the mechanism. Branching occurs during, rather than after, nucleation by Arp2/3 complex activated by the Wiskott-Aldrich syndrome protein (WASP) or Scar protein; capping protein and profilin act synergistically with Arp2/3 complex to favour branched nucleation; phosphate release from aged actin filaments favours dissociation of Arp2/3 complex from the pointed ends of filaments; and branches created by Arp2/3 complex are relatively rigid. These properties result in the automatic assembly of the branched actin network after activation by proteins of the WASP/Scar family and favour the selective disassembly of proximal regions of the network.
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The ARP2/3 complex is responsible for creating branched actin networks through polymerization of actin.
“The seven subunit ARP2/3 complex is responsible for creating branched actin networks through polymerization of actin”
From SHARPIN S146 phosphorylation mediates ARP2/3 interaction, cancer cell invasion and metastasis (2022) · cites this paper as Blanchoin, et al.,2000
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- Authors
- Blanchoin, L., Amann, K. J., Higgs, H. N., Marchand, J.-B., Kaiser, D. A., & Pollard, T. D.
- Affiliations
- Salk Institute for Biological Studies (US)
- Venue
- Nature
- Published
- 2000-04
- Volume
- 404
- Issue
- 6781
- Pages
- 1007-1011
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W1635520329
- Cited by
- 586
- References
- 0
- Citations by year
- 2026: 3 · 2025: 10 · 2024: 18 · 2023: 14 · 2022: 17 · 2021: 14 · 2020: 28 · 2019: 13 · 2018: 20 · 2017: 16 · 2016: 18 · 2015: 27 · 2014: 21 · 2013: 28 · 2012: 20
- FWCI
- 17.65
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- National Institutes of Health
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Microtubule and mitosis dynamics
- Keywords
- actin filament nucleation, Arp2/3 complex, wasps, actin filament branching, pseudopod extension, capping protein, profilin, cell motility
- MeSH terms
- Acanthamoeba, Actins, Animals, Cattle, Contractile Proteins, Cytoskeletal Proteins, Humans, Microfilament Proteins, Nucleotides, Proteins, Rabbits, Recombinant Proteins, Muscle, Skeletal, Wiskott-Aldrich Syndrome Protein Family, Profilins, Wiskott-Aldrich Syndrome Protein, Actin Depolymerizing Factors, Destrin, Actin-Related Protein 2, Actin-Related Protein 3
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