17Beta-estradiol protects against oxidative stress-induced cell death through the glutathione/glutaredoxin-dependent redox regulation of Akt in myocardiac H9c2 cells

J Biol Chem. 2006 May 12;281(19):13092-102. doi: 10.1074/jbc.M601984200. Epub 2006 Mar 20.

Abstract

The GSH/glutaredoxin (GRX) system is involved in the redox regulation of certain enzyme activities, and this system protects cells from H2O2-induced apoptosis by regulating the redox state of Akt (Murata, H., Ihara, Y., Nakamura, H., Yodoi, J., Sumikawa, K., and Kondo, T. (2003) J. Biol. Chem. 278, 50226-50233). Estrogens, such as 17beta-estradiol (E2), play an important role in development, growth, and differentiation and appear to have protective effects on oxidative stress mediated by estrogen receptor alpha (ERalpha). However, the role of the ERbeta-mediated pathway in this cytoprotection and the involvement of E2 in the redox regulation are not well understood. In the present study, we demonstrated that E2 protected cardiac H9c2 cells, expressing ERbeta from H2O2-induced apoptosis concomitant with an increase in the activity of Akt. E2 induced the expression of glutaredoxin (GRX) as well as gamma-glutamylcysteine synthetase, a rate-limiting enzyme for the synthesis of GSH. Inhibitors for both gamma-glutamylcysteine synthetase and GRX and ICI182,780, a specific inhibitor of ERs, abolished the protective effect of E2 on cell survival as well as the activity of Akt, suggesting that ERbeta is involved in the cytoprotection and redox regulation by E2. Transcription of the GRX gene was enhanced by E2. The promoter activity of GRX was up-regulated by an ERbeta-dependent element. These results suggest that the GRX/GSH system is involved in the cytoprotective and genomic effects of E2 on the redox state of Akt, a pathway that is mediated, at least in part, by ERbeta. This mechanism may also play an antiapoptotic role in cancer cells during carcinogenesis or chemotherapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Death / drug effects
  • Cell Line
  • Estradiol / pharmacology*
  • Estrogen Receptor alpha / metabolism
  • Estrogen Receptor beta / metabolism
  • Gene Expression Regulation
  • Glutamate-Cysteine Ligase / genetics
  • Glutamate-Cysteine Ligase / metabolism
  • Glutaredoxins
  • Glutathione / metabolism*
  • Humans
  • Hydrogen Peroxide
  • Molecular Sequence Data
  • Myocytes, Cardiac / drug effects
  • Myocytes, Cardiac / metabolism
  • Oxidation-Reduction / drug effects
  • Oxidative Stress*
  • Oxidoreductases / genetics
  • Oxidoreductases / metabolism*
  • Proto-Oncogene Proteins c-akt / metabolism*
  • Rats

Substances

  • Estrogen Receptor alpha
  • Estrogen Receptor beta
  • GLRX protein, human
  • Glrx protein, rat
  • Glutaredoxins
  • Estradiol
  • Hydrogen Peroxide
  • Oxidoreductases
  • Proto-Oncogene Proteins c-akt
  • Glutamate-Cysteine Ligase
  • Glutathione

Associated data

  • GENBANK/AF167981
  • GENBANK/AY280663
  • GENBANK/BC063166
  • GENBANK/U57439
  • RefSeq/NM_000125
  • RefSeq/NM_001101
  • RefSeq/NM_001437