IL-13 selectively induces vascular cell adhesion molecule-1 expression in human endothelial cells

J Immunol. 1995 Jan 15;154(2):799-803.

Abstract

Previous studies with human umbilical vein endothelial cells (HUVEC) have shown that the cytokine IL-4 induces adherence of human eosinophils, but not neutrophils, because of its ability to selectively induce surface expression of vascular cell adhesion molecule-1 (VCAM-1). Because the cytokine IL-13 shares a number of biologic properties with IL-4, we examined the effect of IL-13 on the expression and function of adhesion molecules on HUVEC. Incubation of HUVEC for 4 to 48 h with IL-13 (0.1 to 15 U/ml) induced surface expression of VCAM-1, as detected by indirect immunofluorescence and flow cytometry, without significantly affecting expression of E-selectin or intercellular adhesion molecule-1. The kinetics and maximal IL-13-induced expression of VCAM-1 were similar to those seen with IL-4. Treatment of HUVEC with an optimal concentration of IL-13 (15 U/ml for 24 h) induced adhesiveness for eosinophils, but not for neutrophils, and adhesion was completely inhibited by mAb recognizing VCAM-1 or alpha 4 integrin (CD49d). These results demonstrate that IL-13, like IL-4, selectively stimulates HUVEC to express functional cell surface VCAM-1 and suggest a possible role for IL-13 in promoting VCAM-1/alpha 4 integrin-dependent accumulation of eosinophils during allergic and other inflammatory reactions in vivo.

Publication types

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

MeSH terms

  • Cell Adhesion / physiology*
  • Cell Adhesion Molecules / biosynthesis
  • Cell Adhesion Molecules / physiology*
  • Cells, Cultured
  • Endothelium, Vascular / metabolism*
  • Eosinophils / physiology
  • Humans
  • Integrin alpha4
  • Integrins / biosynthesis
  • Integrins / physiology
  • Interleukin-13 / physiology*
  • Neutrophils / physiology
  • Umbilical Veins / cytology
  • Vascular Cell Adhesion Molecule-1

Substances

  • Cell Adhesion Molecules
  • Integrins
  • Interleukin-13
  • Vascular Cell Adhesion Molecule-1
  • Integrin alpha4