The heparan sulfate proteoglycan form of epithelial CD44v3 serves as a CD11b/CD18 counter-receptor during polymorphonuclear leukocyte transepithelial migration

J Biol Chem. 2009 Feb 6;284(6):3768-76. doi: 10.1074/jbc.M807805200. Epub 2008 Dec 10.

Abstract

Leukocyte beta2-integrin CD11b/CD18 mediates the firm adhesion and subsequent transepithelial migration of polymorphonuclear leukocytes, but the identity of its counter-receptor(s) on epithelia remains elusive. Here we identified a monoclonal antibody, clone C3H7, which strongly bound to the basolateral membranes of epithelial cells and inhibited both the adhesion of epithelial cells to immobilized CD11b/CD8 and the transepithelial migration of PMNs in a physiologically relevant basolateral-to-apical direction. C3H7 antigen expression in epithelial monolayers was significantly increased by treatment with proinflammatory cytokine interferon-gamma or a combination of interferon-gamma and tumor necrosis factor-alpha. Up-regulation of C3H7 antigen was also observed in the epithelium of inflamed human colon tissues. Microsequencing and Western blotting of the purified antigen showed it to be CD44 variant 3 (CD44v3), a approximately 160-kDa membrane glycoprotein. Further studies demonstrated that this epithelial CD44v3 specifically binds to CD11b/CD18 through its heparan sulfate moieties. In summary, our study demonstrates for the first time that the heparan sulfate proteoglycan form of epithelial CD44v3 plays a critical role in facilitating PMN recruitment during inflammatory episodes via directly binding to CD11b/CD18.

Publication types

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

MeSH terms

  • Antibodies, Monoclonal / immunology
  • Antibodies, Monoclonal / pharmacology
  • CD11b Antigen / immunology
  • CD11b Antigen / metabolism*
  • CD18 Antigens / immunology
  • CD18 Antigens / metabolism*
  • Caco-2 Cells
  • Cell Movement / drug effects
  • Cell Movement / physiology*
  • Gene Expression Regulation / drug effects
  • Gene Expression Regulation / immunology
  • Heparan Sulfate Proteoglycans / immunology
  • Heparan Sulfate Proteoglycans / metabolism*
  • Humans
  • Hyaluronan Receptors / immunology
  • Hyaluronan Receptors / metabolism*
  • Interferon-gamma / immunology
  • Interferon-gamma / metabolism
  • Interferon-gamma / pharmacology
  • Neutrophils / immunology
  • Neutrophils / metabolism*
  • Protein Binding / drug effects
  • Protein Binding / physiology
  • Tumor Necrosis Factor-alpha / immunology
  • Tumor Necrosis Factor-alpha / metabolism
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Antibodies, Monoclonal
  • CD11b Antigen
  • CD18 Antigens
  • CD44V3,8-10
  • Heparan Sulfate Proteoglycans
  • Hyaluronan Receptors
  • ITGAM protein, human
  • Tumor Necrosis Factor-alpha
  • Interferon-gamma