Citation

  • Authors: Gao, P., Yuan, M., Ma, X., Jiang, W., Zhu, L., Wen, M., Xu, J., Liu, Q., An, H.
  • Year: 2016
  • Journal: Mol Immunol 71 184-91
  • Applications: in vitro / siRNA / INTERFERin
  • Cell type: Mouse peritoneal macrophages
    Description: Mouse primary peritoneal macrophage

Method

Transfection was performed with INTERFERin according to the manufacturer’s instructions.

Abstract

IL-27 is an important regulator of TLR4-activated innate immune. The mechanism by which IL-27 production is regulated in TLR4-activated innate immune remains largely unclear. Here we show that expression of transcription factor Fli-1 at protein level is increased in macrophages following LPS stimulation. Fli-1 overexpression increases LPS-activated IL-27 production in macrophages. Consistently, Fli-1 knockdown inhibits LPS-induced IL-27 production in macrophages. Chromatin immunoprecipitation (ChIP) assay reveals that Fli-1 binds the promoter of IL-27 p28 subunit. Further experiments manifest that Fli-1 binds the region between -250 and -150bp upstream of the transcriptional start site of p28 gene and increases p28 gene promoter-controlled transcription. These results demonstrate that Fli-1 positively regulates IL-27 production in TLR4-activated immune response by promoting transcription of IL-27 p28 gene.

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