E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions

EMBO J. 2005 Mar 23;24(6):1146-56. doi: 10.1038/sj.emboj.7600605. Epub 2005 Mar 3.


Cadherin adhesion molecules are key determinants of morphogenesis and tissue architecture. Nevertheless, the molecular mechanisms responsible for the morphogenetic contributions of cadherins remain poorly understood in vivo. Besides supporting cell-cell adhesion, cadherins can affect a wide range of cellular functions that include activation of cell signalling pathways, regulation of the cytoskeleton and control of cell polarity. To determine the role of E-cadherin in stratified epithelium of the epidermis, we have conditionally inactivated its gene in mice. Here we show that loss of E-cadherin in the epidermis in vivo results in perinatal death of mice due to the inability to retain a functional epidermal water barrier. Absence of E-cadherin leads to improper localization of key tight junctional proteins, resulting in permeable tight junctions and thus altered epidermal resistance. In addition, both Rac and activated atypical PKC, crucial for tight junction formation, are mislocalized. Surprisingly, our results indicate that E-cadherin is specifically required for tight junction, but not desmosome, formation and this appears to involve signalling rather than cell contact formation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cadherins / genetics
  • Cadherins / physiology*
  • Cell Communication / genetics
  • Cell Communication / physiology
  • Desmosomes / metabolism
  • Epidermis / chemistry
  • Epidermis / metabolism*
  • Gene Deletion
  • Genes, Lethal
  • Membrane Proteins / metabolism
  • Mice
  • Mice, Transgenic
  • Protein Kinase C / analysis
  • Protein Kinase C / metabolism
  • Tight Junctions / chemistry
  • Tight Junctions / metabolism*
  • Water / metabolism
  • rac GTP-Binding Proteins / analysis
  • rac GTP-Binding Proteins / metabolism


  • Cadherins
  • Membrane Proteins
  • Water
  • PKC-3 protein
  • Protein Kinase C
  • rac GTP-Binding Proteins