Interleukin-4 inhibits the vascular endothelial growth factor- and basic fibroblast growth factor-induced angiogenesis in vitro

Mol Cells. 2002 Aug 31;14(1):115-21.

Abstract

The role of interleukin-4 (IL-4) in the inflammatory process has emerged recently. In this study, we investigated the effect of IL-4 on the angiogenic process in an in vitro experimental system. IL-4 significantly inhibited the proliferation of human umbilical vein endothelial cells (HUVEC) that was induced by the vascular endothelial growth factor (VEGF) and basic fibroblast growth factor (bFGF). VEGF- or bFGF-induced HUVEC chemotaxis was abrogated by the IL-4 treatment. In addition, the formation of tube-like structures by HUVEC in the presence of VEGF or bFGF was also severely down-regulated by IL-4. The inhibitory effects on the critical steps of angiogenesis were not observed with IL-6 that is abundantly found in the inflamed tissue. Our results suggest that IL-4 may play a regulatory role in normal physiology and provide the potential possibility for IL-4 as a therapeutic agent in the intervention of angiogenesis-related diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chemotaxis / drug effects
  • Down-Regulation
  • Drug Antagonism
  • Endothelial Growth Factors / pharmacology*
  • Fibroblast Growth Factor 2 / pharmacology*
  • Humans
  • In Vitro Techniques
  • Intercellular Signaling Peptides and Proteins / pharmacology*
  • Interleukin-4 / pharmacology*
  • Lymphokines / pharmacology*
  • Neovascularization, Physiologic / drug effects*
  • Neovascularization, Physiologic / physiology
  • Vascular Endothelial Growth Factor A
  • Vascular Endothelial Growth Factors

Substances

  • Endothelial Growth Factors
  • Intercellular Signaling Peptides and Proteins
  • Lymphokines
  • Vascular Endothelial Growth Factor A
  • Vascular Endothelial Growth Factors
  • Fibroblast Growth Factor 2
  • Interleukin-4