Heterogenous glycosylation of ICAM-3 and lack of interaction with Mac-1 and p150,95

Eur J Immunol. 1995 Apr;25(4):1008-12. doi: 10.1002/eji.1830250422.

Abstract

Intercellular adhesion molecule (ICAM)-1, ICAM-2, and ICAM-3 have been identified as counter-receptors for the leukocyte integrin lymphocyte function-associated antigen 1 (LFA-1). The other leukocyte integrins, Mac-1 and p150,95, also interact with ICAM-1. ICAM-1 and ICAM-3 are highly homologous, and an undefined ligand for Mac-1 is present on neutrophils where ICAM-3 is well expressed. In addition, glycosylation has been shown to affect the interaction of ICAM-1 with Mac-1. We therefore sought to characterize ICAM-3 heterogeneity and determine whether ICAM-3 was a ligand for either Mac-1 or p150,95. Despite extensive differences in N-linked glycosylation, ICAM-3 purified from lymphoid cells and from neutrophils supports adhesion of LFA-1-bearing cells equally well; however, neither supports adhesion of Mac-1 or p150,95-expressing chinese hamster ovary cell transfectants. Similarly, purified Mac-1 does not support adhesion of ICAM-2 or ICAM-3-expressing L cell transfectants. ICAM-3 on neutrophils does not participate in Mac-1-dependent homotypic aggregation. Thus, ICAM-3 is not a counter-receptor for either Mac-1 or p150,95.

Publication types

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

MeSH terms

  • Animals
  • Antigens, CD*
  • Antigens, Differentiation*
  • CHO Cells
  • Cell Adhesion
  • Cell Adhesion Molecules / chemistry*
  • Cell Adhesion Molecules / metabolism
  • Cricetinae
  • Glycosylation
  • Humans
  • Integrin alphaXbeta2 / metabolism*
  • Macrophage-1 Antigen / metabolism*
  • Neutrophils / cytology
  • Neutrophils / metabolism

Substances

  • Antigens, CD
  • Antigens, Differentiation
  • Cell Adhesion Molecules
  • ICAM3 protein, human
  • Integrin alphaXbeta2
  • Macrophage-1 Antigen