Interleukin-2 receptor beta subunit-dependent and -independent regulation of intestinal epithelial tight junctions

J Biol Chem. 2001 Sep 21;276(38):35571-80. doi: 10.1074/jbc.M106013200. Epub 2001 Jul 20.

Abstract

Interleukin (IL)-15 is able to regulate tight junction formation in intestinal epithelial cells. However, the mechanisms that regulate the intestinal barrier function in response to IL-15 and the involved subunits of the IL-15 ligand-receptor system are unknown. We determined the IL-2Rbeta subunit and IL-15-dependent regulation of tight junction-associated proteins in the human intestinal epithelial cell line T-84. The IL-2Rbeta subunit was expressed and induced signal transduction in caveolin enriched rafts in intestinal epithelial cells. IL-15-mediated tightening of intestinal epithelial monolayers correlated with the enhanced recruitment of tight junction proteins into Triton X-100-insoluble protein fractions. IL-15-mediated up-regulation of ZO-1 and ZO-2 expression was independent of the IL-2Rbeta subunit, whereas the phosphorylation of occludin and enhanced membrane association of claudin-1 and claudin-2 by IL-15 required the presence of the IL-2Rbeta subunit. Recruitment of claudins and hyperphosphorylated occludin into tight junctions resulted in a more marked induction of tight junction formation in intestinal epithelial cells than the up-regulation of ZO-1 and ZO-2 by itself. The regulation of the intestinal epithelial barrier function by IL-15 involves IL-2Rbeta-dependent and -independent signaling pathways leading to the recruitment of claudins, hyperphosphorylated occludin, ZO-1, and ZO-2 into the tight junctional protein complex.

Publication types

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

MeSH terms

  • Base Sequence
  • Caveolin 1
  • Caveolins / physiology
  • DNA Primers
  • Humans
  • Interleukin-15 / physiology
  • Intestinal Mucosa / physiology*
  • Membrane Proteins / physiology
  • Phosphoproteins / physiology
  • Phosphorylation
  • Receptors, Interleukin-2 / physiology*
  • Signal Transduction
  • Tight Junctions / physiology*
  • Transfection
  • Tumor Cells, Cultured
  • Up-Regulation / physiology
  • Zonula Occludens-1 Protein
  • Zonula Occludens-2 Protein

Substances

  • CAV1 protein, human
  • Caveolin 1
  • Caveolins
  • DNA Primers
  • Interleukin-15
  • Membrane Proteins
  • Phosphoproteins
  • Receptors, Interleukin-2
  • TJP1 protein, human
  • TJP2 protein, human
  • Zonula Occludens-1 Protein
  • Zonula Occludens-2 Protein