E-cadherin is critical for collective sheet migration and is regulated by the chemokine CXCL12 protein during restitution

J Biol Chem. 2012 Jun 22;287(26):22227-40. doi: 10.1074/jbc.M112.367979. Epub 2012 May 1.

Abstract

Chemokines and other immune mediators enhance epithelial barrier repair. The intestinal barrier is established by highly regulated cell-cell contacts between epithelial cells. The goal of these studies was to define the role for the chemokine CXCL12 in regulating E-cadherin during collective sheet migration during epithelial restitution. Mechanisms regulating E-cadherin were investigated using Caco2(BBE) and IEC-6 model epithelia. Genetic knockdown confirmed a critical role for E-cadherin in in vitro restitution and in vivo wound repair. During restitution, both CXCL12 and TGF-β1 tightened the monolayer by decreasing the paracellular space between migrating epithelial cells. However, CXCL12 differed from TGF-β1 by stimulating the significant increase in E-cadherin membrane localization during restitution. Chemokine-stimulated relocalization of E-cadherin was paralleled by an increase in barrier integrity of polarized epithelium during restitution. CXCL12 activation of its cognate receptor CXCR4 stimulated E-cadherin localization and monolayer tightening through Rho-associated protein kinase activation and F-actin reorganization. These data demonstrate a key role for E-cadherin in intestinal epithelial restitution.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Actins / metabolism
  • Adherens Junctions / metabolism
  • Animals
  • Caco-2 Cells
  • Cadherins / metabolism*
  • Cell Movement
  • Chemokine CXCL12 / metabolism*
  • Chemokines / metabolism
  • Epithelium / metabolism
  • Gene Deletion
  • Heterozygote
  • Humans
  • Intestinal Mucosa / metabolism
  • Microscopy, Confocal / methods
  • Rats
  • Recombinant Proteins / metabolism
  • Wound Healing

Substances

  • Actins
  • Cadherins
  • Chemokine CXCL12
  • Chemokines
  • Recombinant Proteins