Forced IFIT-2 expression represses LPS induced TNF-alpha expression at posttranscriptional levels

BMC Immunol. 2008 Dec 24:9:75. doi: 10.1186/1471-2172-9-75.

Abstract

Background: Interferon induced tetratricopeptide repeat protein 2 (IFIT-2, P54) belongs to the type I interferon response genes and is highly induced after stimulation with LPS. The biological function of this protein is so far unclear. Previous studies indicated that IFIT-2 binds to the initiation factor subunit eIF-3c, affects translation initiation and inhibits protein synthesis. The aim of the study was to further characterize the function of IFIT-2.

Results: Stimulation of RAW264.7 macrophages with LPS or IFN-gamma leads to the expression of IFIT-2 in a type I interferon dependent manner. By using stably transfected RAW264.7 macrophages overexpressing IFIT-2 we found that IFIT-2 inhibits selectively LPS induced expression of TNF-alpha, IL-6, and MIP-2 but not of IFIT-1 or EGR-1. In IFIT-2 overexpressing cells TNF-alpha mRNA expression was lower after LPS stimulation due to reduced mRNA stability. Further experiments suggest that characteristics of the 3'UTR of transcripts discriminate whether IFIT-2 has a strong impact on protein expression or not.

Conclusion: Our data suggest that IFIT-2 may affect selectively LPS induced protein expression probably by regulation at different posttranscriptional levels.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3' Untranslated Regions
  • Adaptor Proteins, Signal Transducing
  • Animals
  • Apoptosis Regulatory Proteins
  • Carrier Proteins / genetics
  • Cell Line
  • Chemokine CXCL2 / genetics
  • Chemokine CXCL2 / metabolism
  • Immunity, Innate / drug effects*
  • Immunity, Innate / genetics
  • Interferon-beta / immunology
  • Interleukin-6 / genetics
  • Interleukin-6 / metabolism
  • Lipopolysaccharides / pharmacology*
  • Macrophages / drug effects
  • Macrophages / immunology
  • Macrophages / metabolism*
  • Mice
  • Protein Binding
  • Protein Biosynthesis*
  • Proteins / genetics
  • Proteins / immunology
  • Proteins / metabolism*
  • RNA Processing, Post-Transcriptional
  • RNA Stability / genetics
  • RNA Stability / immunology
  • RNA, Messenger / analysis
  • RNA, Messenger / chemistry
  • RNA-Binding Proteins
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / immunology
  • Recombinant Fusion Proteins / metabolism
  • Regulatory Sequences, Ribonucleic Acid
  • Sequence Deletion
  • Transcriptional Activation / immunology*
  • Transfection
  • Transgenes
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • 3' Untranslated Regions
  • Adaptor Proteins, Signal Transducing
  • Apoptosis Regulatory Proteins
  • Carrier Proteins
  • Chemokine CXCL2
  • Cxcl2 protein, mouse
  • Ifit1 protein, mouse
  • Ifit2 protein, mouse
  • Interleukin-6
  • Lipopolysaccharides
  • Proteins
  • RNA, Messenger
  • RNA-Binding Proteins
  • Recombinant Fusion Proteins
  • Regulatory Sequences, Ribonucleic Acid
  • Tumor Necrosis Factor-alpha
  • Interferon-beta