Activation of the repulsive receptor Roundabout inhibits N-cadherin-mediated cell adhesion

Nat Cell Biol. 2002 Oct;4(10):798-805. doi: 10.1038/ncb858.

Abstract

The formation of axon trajectories requires integration of local adhesive interactions with directional information from attractive and repulsive cues. Here, we show that these two types of information are functionally integrated; activation of the transmembrane receptor Roundabout (Robo) by its ligand, the secreted repulsive guidance cue Slit, inactivates N-cadherin-mediated adhesion. Loss of N-cadherin-mediated adhesion is accompanied by tyrosine phosphorylation of beta-catenin and its loss from the N-cadherin complex, concomitant with the formation of a supramolecular complex containing Robo, Abelson (Abl) kinase and N-cadherin. Local formation of such a receptor complex is an ideal mechanism to steer the growth cone while still allowing adhesion and growth in other directions.

Publication types

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

MeSH terms

  • Animals
  • Cadherins / genetics
  • Cadherins / metabolism*
  • Cell Adhesion / physiology*
  • Cell Communication / physiology
  • Cell Differentiation / physiology
  • Cell Membrane / metabolism*
  • Cells, Cultured
  • Central Nervous System / embryology
  • Central Nervous System / metabolism*
  • Chick Embryo
  • Cytoskeletal Proteins / genetics
  • Cytoskeletal Proteins / metabolism
  • Fibroblasts
  • Glycoproteins / deficiency
  • Glycoproteins / genetics
  • Growth Cones / metabolism*
  • Macromolecular Substances
  • Mice
  • Nerve Tissue Proteins / deficiency
  • Nerve Tissue Proteins / genetics
  • Peptide Fragments
  • Protein Structure, Tertiary / physiology
  • Proto-Oncogene Proteins c-abl / genetics
  • Proto-Oncogene Proteins c-abl / metabolism
  • Receptors, Immunologic / genetics
  • Receptors, Immunologic / metabolism*
  • Retina
  • Roundabout Proteins
  • Trans-Activators / genetics
  • Trans-Activators / metabolism
  • beta Catenin

Substances

  • CTNNB1 protein, mouse
  • Cadherins
  • Cytoskeletal Proteins
  • Glycoproteins
  • Macromolecular Substances
  • Nerve Tissue Proteins
  • Peptide Fragments
  • Receptors, Immunologic
  • Trans-Activators
  • beta Catenin
  • slit protein, vertebrate
  • Proto-Oncogene Proteins c-abl