P-selectin glycoprotein ligand-1 (PSGL-1) is a ligand for L-selectin in neutrophil aggregation

Blood. 1996 Oct 1;88(7):2415-21.

Abstract

In inflammation, activated neutrophils adhere to endothelial cells and aggregate with one another. While beta 2-integrin and L-selectin are essential for aggregation, their ligands remain to be identified. We have previously shown that L-selectin mediates a carbohydrate-dependent interaction in aggregation (Simon et al: J Immunol 149:2765, 1992; Rochon et al: J Immunol 152:1385, 1994). We have suggested that the L-selectin counter-structure is a mucinlike protein and proposed that aggregation occurs through a two-step process involving L-selectin, beta 2-integrin, and their distinct counter-structures (Bennett et al: J Leuk Biol 58:510, 1995). A candidate ligand for L-selectin is P-selectin glycoprotein ligand-1 (PSGL-1), a mucinlike protein on neutrophils that binds P-and E-selectin. Using flow cytometry we show that the number and size of neutrophil aggregates is reduced with Fab fragments of PL1, an anti-PSGL-1 monoclonal antibody that blocks the interaction between P-selectin and PSGL-1 (Moore et al: J Cell Biol 128:661, 1995). In addition, monoclonal antibodies to L-selectin and PSGL-1 were used simultaneously to modulate the availability of these adhesion molecules on individual cell populations. The inhibition of aggregation by these antibodies is consistent with L-selectin and PSGL-1 being counter-structures. We suggest that L-selectin and PSGL-1 support a collisional cell-cell interaction that represents the first step in neutrophil aggregation.

Publication types

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

MeSH terms

  • Antibodies, Monoclonal / immunology
  • Antibodies, Monoclonal / pharmacology
  • CD18 Antigens / physiology
  • Cell Adhesion
  • Cell Aggregation / physiology*
  • Flow Cytometry
  • Humans
  • Immunoglobulin Fab Fragments / pharmacology
  • L-Selectin / physiology*
  • Ligands
  • Lipopolysaccharides / pharmacology
  • Membrane Glycoproteins / immunology
  • Membrane Glycoproteins / physiology*
  • Metalloendopeptidases / pharmacology
  • N-Formylmethionine Leucyl-Phenylalanine / pharmacology
  • Neutrophils / cytology*
  • Neutrophils / metabolism

Substances

  • Antibodies, Monoclonal
  • CD18 Antigens
  • Immunoglobulin Fab Fragments
  • Ligands
  • Lipopolysaccharides
  • Membrane Glycoproteins
  • P-selectin ligand protein
  • L-Selectin
  • N-Formylmethionine Leucyl-Phenylalanine
  • Metalloendopeptidases
  • O-sialoglycoprotein endopeptidase