PUBLICATION

Load Adaptation of Lamellipodial Actin Networks

Authors
Mueller, J., Szep, G., Nemethova, M., de Vries, I., Lieber, A.D., Winkler, C., Kruse, K., Small, J.V., Schmeiser, C., Keren, K., Hauschild, R., Sixt, M.
ID
ZDB-PUB-171011-22
Date
2017
Source
Cell   171: 188-200.e16 (Journal)
Registered Authors
Keywords
actin dynamics, actin network, cell mechanics, cell migration, correlated electron tomography, cytoskeleton, keratocyte, lamellipodium, membrane tension
MeSH Terms
  • Actin Cytoskeleton/chemistry*
  • Actin Cytoskeleton/ultrastructure*
  • Animals
  • Cell Membrane/chemistry
  • Keratinocytes/chemistry
  • Keratinocytes/ultrastructure*
  • Microscopy, Electron
  • Pseudopodia/chemistry*
  • Pseudopodia/ultrastructure*
  • Zebrafish
PubMed
28867286 Full text @ Cell
Abstract
Actin filaments polymerizing against membranes power endocytosis, vesicular traffic, and cell motility. In vitro reconstitution studies suggest that the structure and the dynamics of actin networks respond to mechanical forces. We demonstrate that lamellipodial actin of migrating cells responds to mechanical load when membrane tension is modulated. In a steady state, migrating cell filaments assume the canonical dendritic geometry, defined by Arp2/3-generated 70° branch points. Increased tension triggers a dense network with a broadened range of angles, whereas decreased tension causes a shift to a sparse configuration dominated by filaments growing perpendicularly to the plasma membrane. We show that these responses emerge from the geometry of branched actin: when load per filament decreases, elongation speed increases and perpendicular filaments gradually outcompete others because they polymerize the shortest distance to the membrane, where they are protected from capping. This network-intrinsic geometrical adaptation mechanism tunes protrusive force in response to mechanical load.
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