The cutaneous lymphocyte antigen is an essential component of the L-selectin ligand induced on human vascular endothelial cells

J Exp Med. 1999 Jan 18;189(2):241-52. doi: 10.1084/jem.189.2.241.

Abstract

L-selectin mediates leukocyte rolling on vascular endothelium during inflammation. Although vascular endothelium can be activated with inflammatory cytokines to express functional L-selectin ligands, these ligands have not been well characterized. In this study, fucosyltransferase VII cDNA (Fuc-TVII) transfection of the EA.hy926 human vascular endothelial cell line (926-FtVII) induced functional L-selectin ligand expression and expression of sialyl Lewisx (sLex), as defined by HECA-452 (cutaneous lymphocyte antigen; CLA) and CSLEX-1 mAbs. Cytokine activation of human umbilical vein endothelial cells (HUVEC) also induced functional L-selectin ligand expression, with increased CLA expression and Fuc-TVII transcription. The majority of L-selectin-dependent lymphocyte attachment to activated HUVEC and 926-FtVII cells was blocked specifically by treating the endothelial cells with the HECA-452 mAb, but not the CSLEX-1 mAb. CLA-bearing ligands on vascular endothelium also required sulfation and appropriate molecular scaffolds for functional activity, but were distinct from the L-selectin ligands previously identified by the MECA-79 mAb. These findings demonstrate that the HECA-452- defined antigen, CLA, is an essential carbohydrate component of vascular L-selectin ligands.

Publication types

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

MeSH terms

  • Antibodies, Monoclonal / immunology
  • Antigens, Differentiation, T-Lymphocyte
  • Antigens, Neoplasm
  • Cell Adhesion / immunology
  • Cell Line
  • Endothelium, Vascular / immunology*
  • Fluorescent Antibody Technique
  • Fucosyltransferases / genetics
  • Humans
  • Immunoglobulin M / genetics
  • Immunoglobulin M / immunology
  • Inflammation / immunology
  • L-Selectin / immunology*
  • Leukocytes / immunology
  • Ligands*
  • Lymphocytes / metabolism
  • Membrane Glycoproteins / immunology*
  • Oligosaccharides / immunology
  • Recombinant Fusion Proteins / genetics
  • Sialyl Lewis X Antigen
  • Transfection / genetics
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Antibodies, Monoclonal
  • Antigens, Differentiation, T-Lymphocyte
  • Antigens, Neoplasm
  • CTAGE1 protein, human
  • Immunoglobulin M
  • Ligands
  • Membrane Glycoproteins
  • Oligosaccharides
  • Recombinant Fusion Proteins
  • Sialyl Lewis X Antigen
  • Tumor Necrosis Factor-alpha
  • L-Selectin
  • Fucosyltransferases