Regulation of IL-10 gene expression in Th2 cells by Jun proteins

J Immunol. 2005 Feb 15;174(4):2098-105. doi: 10.4049/jimmunol.174.4.2098.

Abstract

IL-10 is a key regulatory cytokine produced by T lymphocytes. Although Th2 cells are a major source of IL-10, little is known about IL-10 gene regulation in Th2 cells. High levels of IL-10 mRNA transcription are induced in the Th2 clone D10 after PMA plus ionomycin (P/I) stimulation; however we found that the IL-10 promoter was not inducible by P/I in D10 cells. We therefore sought regulatory regions in the IL-10 gene that could promote P/I-activated transcription in Th2 cells. Two strong DNase I-hypersensitive sites (DHSSs) were identified in the IL-10 gene in mouse T cells, and conserved noncoding sequences (CNSs) between the mouse and human IL-10 genes were also identified. One IL-10 DHSS maps within or next to a highly conserved CNS region, CNS-3. The CNS-3 region contains an AP-1 site that binds JunB and c-Jun proteins specifically in Th2 cells and not in Th1 cells. The CNS-3 element activates transcription from the IL-10 promoter after P/I stimulation and is responsive to c-Jun and JunB. Retroviral mediated-expression of either c-Jun or JunB in primary T cells led to a large increase in IL-10 expression, and inhibition of AP-1 activity by a dominant negative form of c-Jun in primary T cells strongly repressed IL-10 expression. IFN-gamma was relatively unaffected by modulations in AP-1 activity. These data indicate that we have identified a novel regulatory element that can specifically activate transcription of the IL-10 gene in Th2 cells via the AP-1/Jun pathway.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Base Sequence
  • Cell Line
  • Cell Line, Tumor
  • Cells, Cultured
  • Chromatin / genetics
  • Chromatin / metabolism
  • Clone Cells
  • Conserved Sequence
  • Deoxyribonuclease I / genetics
  • Gene Expression Regulation / immunology*
  • Humans
  • Interleukin-10 / biosynthesis*
  • Interleukin-10 / genetics*
  • Interleukin-10 / metabolism
  • Mice
  • Molecular Sequence Data
  • NIH 3T3 Cells
  • Protein Binding
  • Proto-Oncogene Proteins c-jun / metabolism
  • Proto-Oncogene Proteins c-jun / physiology*
  • Regulatory Sequences, Nucleic Acid
  • Th2 Cells / immunology*
  • Th2 Cells / metabolism*
  • Transcription Factor AP-1 / metabolism
  • Transcription Factor AP-1 / physiology

Substances

  • Chromatin
  • Proto-Oncogene Proteins c-jun
  • Transcription Factor AP-1
  • Interleukin-10
  • Deoxyribonuclease I