Activation of peripheral blood T cells by interaction and migration through endothelium: role of lymphocyte function antigen-1/intercellular adhesion molecule-1 and interleukin-15

Blood. 1999 Feb 1;93(3):886-96.

Abstract

Cell adhesion molecules have a key role in the migration of T cells to inflammatory foci. However, the effect of the endothelial-lymphocyte interaction on the activation of the latter cells remains unresolved. We have studied the effect of resting and stimulated endothelial cells (ECs) on the activation of peripheral blood T cells (PBTLs), as assessed by the expression of CD69 and CD25 activation antigens. The incubation of PBTLs with tumor necrosis factor-alpha-activated EC monolayers, either alive or fixed, induced the expression of CD69 but not CD25, preferentially in the CD8(+) CD45RO+ cell subset. Furthermore, it induced the production of cytokines such as IFN-gamma, but not that of interleukin-2 (IL-2) and IL-4. EC treated with other stimuli such as IL-1beta, IFN-gamma, or lipopolysaccharide also showed the same proactivatory effect on T cells. Lymphocyte activation was almost completely inhibited by blocking anti-CD18 and anti-intercellular adhesion molecule-1 (anti-ICAM-1) monoclonal antibodies (MoAbs), but only slightly affected by MoAbs against CD49d, vascular cell adhesion molecule-1, and anti-IL-15. In addition, the interaction of PBTL with immobilized ICAM-1 induced CD69 expression in the same memory T-cell subset. IL-15 induced T-cell activation with expression of CD69 and CD25, and production of IFN-gamma, and its effect was additive with that triggered by cell adhesion to either EC or immobilized ICAM-1. The transmigration of PBTLs through either confluent EC monolayers or ICAM-1-coated membranes also induced efficiently the expression of CD69. When IL-15 was used as chemoattractant in these assays, a further enhancement in CD69 expression was observed in migrated cells. Together these results indicate that stimulated endothelium may have an important role in T-cell activation, through the lymphocyte function antigen-1/ICAM-1 pathway, and that IL-15 efficiently cooperates in this phenomenon. These observations could account for the abundance of CD69(+) cells in the lymphocytic infiltrates of several chronic inflammatory diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Monoclonal / pharmacology
  • Antigens, CD / biosynthesis
  • Antigens, Differentiation, T-Lymphocyte / biosynthesis
  • CD18 Antigens / physiology
  • Cell Adhesion
  • Cell Movement
  • Chemokine CCL4
  • Chemotaxis, Leukocyte
  • Humans
  • Immunologic Memory
  • Intercellular Adhesion Molecule-1 / physiology*
  • Interferon-gamma / biosynthesis
  • Interferon-gamma / pharmacology
  • Interleukin-1 / pharmacology
  • Interleukin-15 / pharmacology
  • Interleukin-15 / physiology*
  • Lectins, C-Type
  • Leukocyte Common Antigens / analysis
  • Lipopolysaccharides / pharmacology
  • Lymphocyte Activation* / drug effects
  • Lymphocyte Function-Associated Antigen-1 / physiology*
  • Macrophage Inflammatory Proteins / pharmacology
  • Membrane Glycoproteins / biosynthesis
  • Mice
  • Receptors, G-Protein-Coupled
  • T-Lymphocyte Subsets / cytology
  • T-Lymphocyte Subsets / drug effects
  • T-Lymphocyte Subsets / immunology*

Substances

  • ADGRE5 protein, human
  • Adgre5 protein, mouse
  • Antibodies, Monoclonal
  • Antigens, CD
  • Antigens, Differentiation, T-Lymphocyte
  • CD18 Antigens
  • CD69 antigen
  • Chemokine CCL4
  • Interleukin-1
  • Interleukin-15
  • Lectins, C-Type
  • Lipopolysaccharides
  • Lymphocyte Function-Associated Antigen-1
  • Macrophage Inflammatory Proteins
  • Membrane Glycoproteins
  • Receptors, G-Protein-Coupled
  • Intercellular Adhesion Molecule-1
  • Interferon-gamma
  • Leukocyte Common Antigens