Actin flow-dependent and -independent force transmission through integrins

Proc Natl Acad Sci U S A. 2020 Dec 22;117(51):32413-32422. doi: 10.1073/pnas.2010292117. Epub 2020 Dec 1.

Abstract

Integrin-dependent adhesions mediate reciprocal exchange of force and information between the cell and the extracellular matrix. These effects are attributed to the "focal adhesion clutch," in which moving actin filaments transmit force to integrins via dynamic protein interactions. To elucidate these processes, we measured force on talin together with actin flow speed. While force on talin in small lamellipodial adhesions correlated with actin flow, talin tension in large adhesions further from the cell edge was mainly flow-independent. Stiff substrates shifted force transfer toward the flow-independent mechanism. Flow-dependent force transfer required talin's C-terminal actin binding site, ABS3, but not vinculin. Flow-independent force transfer initially required vinculin and at later times the central actin binding site, ABS2. Force transfer through integrins thus occurs not through a continuous clutch but through a series of discrete states mediated by distinct protein interactions, with their ratio modulated by substrate stiffness.

Keywords: focal adhesion; stiffness sensing; talin.

Publication types

  • Research Support, N.I.H., Extramural
  • Video-Audio Media

MeSH terms

  • Actins / genetics
  • Actins / metabolism*
  • Animals
  • Binding Sites
  • Fluorescence Resonance Energy Transfer
  • Focal Adhesions / physiology
  • Integrins / metabolism*
  • Mice
  • Mutation
  • NIH 3T3 Cells
  • Talin / genetics
  • Talin / metabolism
  • Time-Lapse Imaging
  • Vinculin / genetics
  • Vinculin / metabolism

Substances

  • Actins
  • Integrins
  • Talin
  • Vcl protein, mouse
  • Tln1 protein, mouse
  • Vinculin