JAM-A regulates epithelial proliferation through Akt/β-catenin signalling

EMBO Rep. 2011 Apr;12(4):314-20. doi: 10.1038/embor.2011.16. Epub 2011 Mar 4.

Abstract

Expression of the tight junction protein junctional adhesion molecule-A (JAM-A) has been linked to proliferation and tumour progression. However, a direct role for JAM-A in regulating proliferative processes has not been shown. By using complementary in vivo and in vitro approaches, we demonstrate that JAM-A restricts intestinal epithelial cell (IEC) proliferation in a dimerization-dependent manner, by inhibiting Akt-dependent β-catenin activation. Furthermore, IECs from transgenic JAM-A(-/-)/β-catenin/T-cell factor reporter mice showed enhanced β-catenin-dependent transcription. Finally, inhibition of Akt reversed colonic crypt hyperproliferation in JAM-A-deficient mice. These data establish a new link between JAM-A and IEC homeostasis.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Adhesion Molecules / genetics
  • Cell Adhesion Molecules / metabolism*
  • Cell Line
  • Cell Proliferation / drug effects
  • Epithelial Cells / cytology*
  • Epithelial Cells / metabolism*
  • Humans
  • Immunoblotting
  • Mice
  • Mice, Mutant Strains
  • Phosphorylation / drug effects
  • Proto-Oncogene Proteins c-akt / antagonists & inhibitors
  • Proto-Oncogene Proteins c-akt / metabolism*
  • Receptors, Cell Surface / genetics
  • Receptors, Cell Surface / metabolism*
  • Ribonucleosides / pharmacology
  • Signal Transduction / genetics
  • Signal Transduction / physiology*
  • Tight Junctions / genetics
  • Tight Junctions / metabolism
  • beta Catenin / genetics
  • beta Catenin / metabolism*

Substances

  • Cell Adhesion Molecules
  • F11r protein, mouse
  • Receptors, Cell Surface
  • Ribonucleosides
  • beta Catenin
  • triciribine
  • Proto-Oncogene Proteins c-akt