Activation of Nrf2 is required for up-regulation of the π class of glutathione S-transferase in rat primary hepatocytes with L-methionine starvation

J Agric Food Chem. 2012 Jul 4;60(26):6537-45. doi: 10.1021/jf301567m. Epub 2012 Jun 22.

Abstract

Numerous genes expression is regulated in response to amino acid shortage, which helps organisms adapt to amino acid limitation. The expression of the π class of glutathione (GSH) S-transferase (GSTP), a highly inducible phase II detoxification enzyme, is regulated mainly by activates activating protein 1 (AP-1) binding to the enhancer I of GSTP (GPEI). Here we show the critical role of nuclear factor erythroid-2-related factor 2 (Nrf2) in up-regulating GSTP gene transcription. Primary rat hepatocytes were cultured in a methionine-restricted medium, and immunoblotting and RT-PCR analyses showed that methionine restriction time-dependently increased GSTP protein and mRNA expression over a 48 h period. Nrf2 translocation to the nucleus, nuclear proteins binding to GPEI, and antioxidant response element (ARE) luciferase reporter activity were increased by methionine restriction as well as by l-buthionine sulfoximine (BSO), a GSH synthesis inhibitor. Transfection with Nrf2 siRNA knocked down Nrf2 expression and reversed the methionine-induced GSTP expression and GPEI binding activity. Chromatin immunoprecipitation assay confirmed the binding of Nrf2 to the GPEI. Phosphorylation of extracellular signal-regulated kinase 2 (ERK2) was increased in methionine-restricted and BSO-treated cells. ERK2 siRNA abolished methionine restriction-induced Nrf2 nuclear translocation, GPEI binding activity, ARE-luciferase reporter activity, and GSTP expression. Our results suggest that the up-regulation of GSTP gene transcription in response to methionine restriction likely occurs via the ERK-Nrf2-GPEI signaling pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Nucleus / metabolism
  • Cells, Cultured
  • Culture Media
  • Gene Expression
  • Glutathione Transferase / analysis
  • Glutathione Transferase / genetics*
  • Hepatocytes / metabolism*
  • Male
  • Methionine / administration & dosage*
  • Mitogen-Activated Protein Kinase 1 / metabolism
  • NF-E2-Related Factor 2 / physiology*
  • RNA, Messenger / analysis
  • Rats
  • Rats, Sprague-Dawley
  • Up-Regulation

Substances

  • Culture Media
  • NF-E2-Related Factor 2
  • RNA, Messenger
  • Methionine
  • Glutathione Transferase
  • Mitogen-Activated Protein Kinase 1