Upregulation of thromboxane synthase mediates visfatin-induced interleukin-8 expression and angiogenic activity in endothelial cells

Biochem Biophys Res Commun. 2012 Feb 24;418(4):662-8. doi: 10.1016/j.bbrc.2012.01.072. Epub 2012 Jan 24.

Abstract

Thromboxane synthase (TXAS) is an enzyme that catalyzes the synthesis of thromboxane A(2) (TXA(2)). Overexpression of TXAS is associated with a variety of vascular diseases. Recently, we reported that visfatin, a novel adipokine, exhibits angiogenic actions. In this study, we showed that visfatin increased mRNA and protein levels of TXAS and stimulated TXA(2) biosynthesis in vascular endothelial cells. In addition, visfatin induced the expression and secretion of interleukin-8 (IL-8), which is blocked by a TXAS inhibitor and by the transfection of siRNA specific for TXAS. Furthermore, the inhibition of TXAS activity and blockade of the IL-8 receptor attenuated visfatin-induced endothelial angiogenesis. Together, these results showed that visfatin promoted IL-8 production by upregulation of TXAS, leading to angiogenic activation in endothelial cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line, Tumor
  • Endothelium, Vascular / metabolism*
  • Gene Expression Regulation*
  • Humans
  • Interleukin-8 / genetics*
  • Neovascularization, Physiologic / genetics*
  • Nicotinamide Phosphoribosyltransferase / metabolism*
  • Thromboxane A2 / biosynthesis*
  • Thromboxane-A Synthase / genetics*
  • Up-Regulation

Substances

  • Interleukin-8
  • Thromboxane A2
  • Nicotinamide Phosphoribosyltransferase
  • Thromboxane-A Synthase