JAM-C is a component of desmosomes and a ligand for CD11b/CD18-mediated neutrophil transepithelial migration

Mol Biol Cell. 2004 Aug;15(8):3926-37. doi: 10.1091/mbc.e04-04-0317. Epub 2004 Jun 11.

Abstract

Neutrophil (PMN) transepithelial migration is dependent on the leukocyte beta(2) integrin CD11b/CD18, yet the identity of epithelial counterreceptors remain elusive. Recently, a JAM protein family member termed JAM-C was implicated in leukocyte adhesive interactions; however, its expression in epithelia and role in PMN-epithelial interactions are unknown. Here, we demonstrate that JAM-C is abundantly expressed basolaterally in intestinal epithelia and localizes to desmosomes but not tight junctions. Desmosomal localization of JAM-C was further confirmed by experiments aimed at selective disruption of tight junctions and desmosomes. In assays of PMN transepithelial migration, both JAM-C mAbs and JAM-C/Fc chimeras significantly inhibited the rate of PMN transmigration. Additional experiments revealed specific binding of JAM-C to CD11b/CD18 and provided evidence of other epithelial ligands for CD11b/CD18. These findings represent the first demonstration of direct adhesive interactions between PMN and epithelial intercellular junctions (desmosomes) that regulate PMN transepithelial migration and also suggest that JAM-C may play a role in desmosomal structure/function.

Publication types

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

MeSH terms

  • Acrylamide / pharmacology
  • CD11b Antigen / metabolism*
  • CD18 Antigens / metabolism*
  • Cell Adhesion Molecules / analysis*
  • Cell Adhesion Molecules / metabolism*
  • Cell Adhesion Molecules / pharmacology
  • Cell Movement / drug effects
  • Cell Movement / physiology*
  • Desmosomes / chemistry*
  • Desmosomes / drug effects
  • Desmosomes / metabolism
  • Egtazic Acid / pharmacology
  • Epithelial Cells / drug effects
  • Epithelial Cells / immunology
  • Epithelial Cells / metabolism
  • Humans
  • Immunoglobulins / analysis*
  • Immunoglobulins / metabolism*
  • Immunoglobulins / pharmacology
  • Intermediate Filaments / drug effects
  • Intestinal Mucosa / immunology
  • Membrane Proteins / analysis*
  • Membrane Proteins / metabolism*
  • Membrane Proteins / pharmacology
  • Neutrophils / drug effects
  • Neutrophils / physiology*

Substances

  • CD11b Antigen
  • CD18 Antigens
  • Cell Adhesion Molecules
  • Immunoglobulins
  • JAM3 protein, human
  • Membrane Proteins
  • Acrylamide
  • Egtazic Acid