Tat-APE1/ref-1 protein inhibits TNF-alpha-induced endothelial cell activation

Biochem Biophys Res Commun. 2008 Mar 28;368(1):68-73. doi: 10.1016/j.bbrc.2008.01.037. Epub 2008 Jan 17.

Abstract

Apurinic/apyrimidinic endonuclease 1/redox factor-1 (APE1/ref-1) is a multifunctional protein involved both in DNA base excision repair and redox regulation. In this study we evaluated the protective role of Tat-mediated APE1/ref-1 transduction on the tumor necrosis factor (TNF)-alpha-activated endothelial activation in cultured human umbilical vein endothelial cells. To construct Tat-APE1/ref-1 fusion protein, human full length of APE1/ref-1 was fused with Tat-protein transduction domain. Purified Tat-APE1/ref-1 fusion protein efficiently transduced cultured endothelial cells in a dose-dependent manner and reached maximum expression at 1h after incubation. Transduced Tat-APE1/ref-1 showed inhibitory activity on the TNF-alpha-induced monocyte adhesion and vascular cell adhesion molecule-1 expression in cultured endothelial cells. These results suggest Tat-APE1/ref-1 might be useful to reduce vascular endothelial activation or vascular inflammatory disorders.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Adhesion
  • Cells, Cultured
  • DNA-(Apurinic or Apyrimidinic Site) Lyase / genetics
  • DNA-(Apurinic or Apyrimidinic Site) Lyase / isolation & purification
  • DNA-(Apurinic or Apyrimidinic Site) Lyase / metabolism*
  • Endothelial Cells / cytology
  • Endothelial Cells / drug effects*
  • Endothelial Cells / metabolism*
  • Gene Products, tat / genetics
  • Gene Products, tat / isolation & purification
  • Gene Products, tat / metabolism*
  • Humans
  • Monocytes / cytology
  • Monocytes / drug effects
  • Monocytes / metabolism
  • Tumor Necrosis Factor-alpha / pharmacology*
  • Vascular Cell Adhesion Molecule-1 / metabolism

Substances

  • Gene Products, tat
  • Tumor Necrosis Factor-alpha
  • Vascular Cell Adhesion Molecule-1
  • APEX1 protein, human
  • DNA-(Apurinic or Apyrimidinic Site) Lyase