Expression of heme oxygenase-1 protects endothelial cells from irradiation-induced apoptosis

Endothelium. 2005 May-Jun;12(3):113-9. doi: 10.1080/10623320500189814.

Abstract

A common side effect of therapeutic use of ionizing irradiation is endothelial cell damage resulting in a variety of clinical complications. Thus, preservation of endothelial function after irradiation could potentially limit toxicity. Using the murine endothelioma cell line bEnd2 we show here that induction of heme oxygenase-1 (HO-1) by cobalt protoporphyrine IX (CoPP) inhibits irradiation-induced apoptosis. In contrast, HO-1 induction by tin protoporphyrine IX (SnPP), a HO-1 inhibitor, does not affect survival after irradiation. The protective effects of CoPP could be partially reversed by blockade of HO-1 function with SnPP after induction by CoPP. Vice versa, blockade of HO-1 function by SnPP was reversible using CoPP. Treatment with CoPP inhibited cytochrome c release induced by irradiation. These results demonstrate that HO-1 induction and activation prior to irradiation inhibits endothelial apoptosis and might be used for possible cell protection in vivo.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Apoptosis / radiation effects*
  • Cell Line
  • Cytochromes c / metabolism
  • Endothelial Cells / enzymology*
  • Enzyme Activation / drug effects
  • Enzyme Activation / radiation effects
  • Heme Oxygenase-1 / metabolism*
  • Metalloporphyrins / pharmacology
  • Mice
  • Radiotherapy / adverse effects
  • X-Rays*

Substances

  • Metalloporphyrins
  • Cytochromes c
  • Heme Oxygenase-1