Prostaglandin E2 inhibits the interleukin-2 promoter activity through down-regulation of the Oct-dependent transcription of the octamer motif

Cell Immunol. 1996 Sep 15;172(2):229-34. doi: 10.1006/cimm.1996.0237.

Abstract

Prostaglandins, mainly those of the E series (PGE), are modulators of immune responses. Indeed PGE2 inhibits T cell activation and the transcription of the interleukin-2 (IL-2) gene, the major T cell growth factor. We observed that PGE2 inhibits IL-2 promoter transcription activity by interfering with signals activating the (-96 to -66 bp) octamer motif. This motif binds Oct-1 and Oct-2 as well as the phorbol ester and calcium ionophore-inducible jun and fos AP-1 factors. The PGE2-dependent down-modulation is observed in the presence of either the endogenous transacting factor Oct-1 or the exogenously expressed Oct-2. PGE2 does not regulate octamer function by influencing the jun and fos mRNA or Oct-1 protein levels or their DNA-binding abilities. Functional dissection of the octamer motif, through mutations of either the AP-1 or the octamer sites, revealed that the AP-1 site is dispensable for PGE2-dependent inhibition which instead may occur through the interference with the Oct-mediated transactivation of the octamer element. Our data suggest that the Oct-octamer interaction is a novel target of the PGE2-induced down-regulation of the IL-2 promoter.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • DNA-Binding Proteins / physiology
  • Dinoprostone / physiology*
  • Down-Regulation / drug effects
  • Down-Regulation / genetics*
  • Down-Regulation / immunology
  • Homeodomain Proteins / biosynthesis
  • Homeodomain Proteins / genetics*
  • Host Cell Factor C1
  • Humans
  • Interleukin-2 / antagonists & inhibitors
  • Interleukin-2 / genetics*
  • Jurkat Cells
  • Octamer Transcription Factor-1
  • Promoter Regions, Genetic / drug effects
  • Promoter Regions, Genetic / immunology*
  • Proto-Oncogene Proteins c-fos / biosynthesis
  • Proto-Oncogene Proteins c-jun / biosynthesis
  • Transcription Factor AP-1 / biosynthesis
  • Transcription Factors / biosynthesis
  • Transcription Factors / genetics*
  • Transcription, Genetic / drug effects
  • Transcription, Genetic / immunology*

Substances

  • DNA-Binding Proteins
  • HCFC1 protein, human
  • Homeodomain Proteins
  • Host Cell Factor C1
  • Interleukin-2
  • Octamer Transcription Factor-1
  • POU2F1 protein, human
  • Proto-Oncogene Proteins c-fos
  • Proto-Oncogene Proteins c-jun
  • Transcription Factor AP-1
  • Transcription Factors
  • Dinoprostone