Subsecond reorganization of the actin network in cell motility and chemotaxis

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Stefan Diez - , Max Planck Institute of Molecular Cell Biology and Genetics (Author)
  • Günther Gerisch - , Max Planck Institute of Biochemistry (Author)
  • Kurt Anderson - , Max Planck Institute of Molecular Cell Biology and Genetics (Author)
  • Annette Müller-Taubenberger - , Max Planck Institute of Biochemistry (Author)
  • Till Bretschneider - , Max Planck Institute of Biochemistry (Author)

Abstract

Actin networks are continuously reorganized in cells that rapidly change their shape. Applying total internal reflection fluorescence microscopy at acquisition rates of 10-20 Hz, we measured an average growth rate of 3 μm·sec-1 for filamentous actin structures throughout the entire substrate-attached cortex of Dictyostelium cells. New filaments often proceed along preexisting ones, resulting in bundle formation concurrent with filament growth. In cells that orientate in a gradient of chemoattractant, prominent assemblies of actin enriched in the Arp2/3 complex are inserted into the network, primarily at the base of filopods that point into the direction of the gradient. We propose that high turnover rates of actin filaments confer the plasticity to the cell cortex that is required for rapid accommodation to external stimuli.

Details

Original languageEnglish
Pages (from-to)7601-7606
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America : PNAS
Volume102
Issue number21
Publication statusPublished - 24 May 2005
Peer-reviewedYes
Externally publishedYes

External IDs

PubMed 15894626
ORCID /0000-0002-0750-8515/work/142235591

Keywords

Research priority areas of TU Dresden

ASJC Scopus subject areas

Keywords

  • Actin polymerization, Arp2/3 complex, Dictyostelium, Latrunculin, Total internal reflection fluorescence

Library keywords