Ligand binding regulates the directed movement of beta1 integrins on fibroblasts

Nature. 1996 Oct 3;383(6599):438-40. doi: 10.1038/383438a0.

Abstract

To enable cells to crawl, adhesion receptors such as integrins must bind to extracellular molecules and simultaneously interact with force-generating components of the cytoskeleton. We show here that the binding of extracellular ligand in living cells induces the attachment of beta1 integrins to the retrograde-moving cytoskeleton. Unliganded integrins are not associated with the rearward-moving cytoskeleton: gold particles attached to beta1 integrin by a monoclonal antibody diffuse in the membrane. However, addition of soluble RGD peptide (single-letter amino-acid code) or the use of fibronectin-coated gold particles causes the attachment of integrins to the rearward-moving cytoskeleton. Deletion of the beta1 cytoplasmic tail blocks cytoskeletal attachment. The directed movement of integrins in response to ligand indicates that ligand binding is the critical step in regulating organized receptor movement on the cell surface and the migration of adherent cells.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • 3T3 Cells
  • Animals
  • Antibodies / immunology
  • Binding Sites
  • Cell Line
  • Cell Movement / physiology*
  • Chickens
  • Cytoskeleton / physiology
  • Fibroblasts / metabolism*
  • Fibroblasts / physiology
  • Fibronectins / metabolism
  • Gold Colloid
  • Integrin beta1 / metabolism*
  • Ligands
  • Mice
  • Oligopeptides / metabolism
  • Protein Binding

Substances

  • Antibodies
  • Fibronectins
  • Gold Colloid
  • Integrin beta1
  • Ligands
  • Oligopeptides
  • arginyl-glycyl-aspartic acid