Interleukin-1 beta induces differential adhesiveness on human endothelial cell surfaces

Biochem Biophys Res Commun. 1994 Jul 29;202(2):866-72. doi: 10.1006/bbrc.1994.2010.

Abstract

The adhesive strength between HL-60 and endothelial cells activated with IL-1 beta was investigated according to the region (area) on the endothelial cell surface where the HL-60 cell was attached (nuclear, junctional, or cytoplasmic). Using a micropipette single-cell manipulation system, we demonstrated that the increase of adhesive force was due to the activation of the endothelial cell with IL-1 beta and a function of the region of the endothelial cell. The increase in adhesion strength due to the increased expression of E-Selectin on the endothelial cell was studied by the addition of monoclonal antibodies against E-Selectin, ICAM-1, VCAM, and PECAM-1. Our findings suggest that the greatest adhesive strength was seen in the junctional region where the antibodies could not block the adhesion. However, the contribution of E-Selectin was significant in the nuclear region.

Publication types

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

MeSH terms

  • Antibodies, Monoclonal / pharmacology
  • Antigens, Differentiation, Myelomonocytic / immunology
  • Antigens, Differentiation, Myelomonocytic / physiology
  • Cell Adhesion Molecules / immunology
  • Cell Adhesion Molecules / physiology
  • Cell Adhesion*
  • Cells, Cultured
  • E-Selectin
  • Endothelium, Vascular / cytology*
  • Humans
  • Intercellular Adhesion Molecule-1
  • Interleukin-1 / pharmacology*
  • Platelet Endothelial Cell Adhesion Molecule-1
  • Tumor Cells, Cultured
  • Umbilical Veins
  • Vascular Cell Adhesion Molecule-1

Substances

  • Antibodies, Monoclonal
  • Antigens, Differentiation, Myelomonocytic
  • Cell Adhesion Molecules
  • E-Selectin
  • Interleukin-1
  • Platelet Endothelial Cell Adhesion Molecule-1
  • Vascular Cell Adhesion Molecule-1
  • Intercellular Adhesion Molecule-1