Regulation of heme oxygenase-1 gene expression through the phosphatidylinositol 3-kinase/PKC-zeta pathway and Sp1

Free Radic Biol Med. 2006 Jul 15;41(2):247-61. doi: 10.1016/j.freeradbiomed.2006.04.002. Epub 2006 Apr 21.

Abstract

The molecular mechanisms involved in modulation of the antioxidant cell defence by survival signals remain largely unexplored. Here, we report a mechanistic connection between the survival signal elicited by nerve growth factor (NGF) and the antioxidant cell defence represented by heme oxygenase-1 (HO-1) at the level of a newly identified Sp1 site in the human ho1 proximal promoter. By using luciferase reporter constructs we identified a PI3K-responsive region containing a GC-box that resembled the response element for Sp1. Indeed, transfection of Sp1-deficient SL2 cells, electrophoretic mobility shift assays, the use of the GC-box binding drug mithramycin, and mutation of the GC-box provided evidence for a Sp1-like site in the PI3K-sensitive region. Then, we observed with the use of a Sp1-Gal4 chimera that PI3K regulates the transactivating capacity of Sp1. Cotransfection of active PI3K and PKC-zeta expression vectors resulted in substantial increase of Sp1 phosphorylation and in synergistic activation of both Sp1-Gal4 and endogenous Sp1. Moreover, these effects were mimicked by cotransfection of active MEK and ERK expression vectors and were blocked by the MEK inhibitor PD98059. Inhibition of HO-1 with Sn protoporphyrin IX and blockage of Sp-1-mediatied upregulation of HO-1 with mithramycin attenuated antioxidant and cytoprotective functions of NGF against hydrogen peroxide. This study elucidates how NGF contributes to protection of target cells against oxidative stress.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Cell Line, Tumor
  • DNA Primers
  • Electrophoretic Mobility Shift Assay
  • Gene Expression Regulation, Enzymologic*
  • Heme Oxygenase-1 / genetics*
  • Humans
  • Nerve Growth Factor / pharmacology
  • Phosphatidylinositol 3-Kinases / metabolism*
  • Polymerase Chain Reaction
  • Promoter Regions, Genetic
  • Protein Kinase C / metabolism*
  • RNA, Small Interfering
  • Rats
  • Sp1 Transcription Factor / metabolism*
  • Transcriptional Activation
  • Up-Regulation

Substances

  • DNA Primers
  • RNA, Small Interfering
  • Sp1 Transcription Factor
  • Nerve Growth Factor
  • Heme Oxygenase-1
  • Phosphatidylinositol 3-Kinases
  • protein kinase C zeta
  • Protein Kinase C