Up-regulation of growth factor independence 1 in endotoxin tolerant macrophages with low secretion of TNF-alpha and IL-6

Inflamm Res. 2010 Oct;59(10):855-60. doi: 10.1007/s00011-010-0197-1. Epub 2010 Apr 17.

Abstract

Objective: Endotoxin tolerance refers to a low response to lipopolysaccharide (LPS). We hypothesized that growth factor independence 1 (Gfi1) involves in the endotoxin tolerance in macrophages.

Methods: Endotoxin tolerance was induced in the RAW264.7 cell line and thioglycolate-elicited murine peritoneal macrophages by incubation with 100 ng/ml LPS for 20 h. Macrophages without the pretreatment were set as control. Both endotoxin tolerant and control cells were then stimulated with 1,000 ng/ml LPS for indicated period of incubation. Gfi1 mRNA expression and protein production were investigated by real-time PCR and Western blotting, respectively. ELISA was performed to quantify the secretion of TNF-alpha and IL-6.

Result: Compared with non-endotoxin tolerant macrophages, endotoxin tolerant cells secreted a lower amount of TNF-alpha and IL-6. The mRNA expression of Gfi1 in endotoxin tolerant macrophages was higher than that of control in both RAW264.7 cells and thioglycolate-elicited murine peritoneal macrophages. The protein production was accordingly up-regulated in endotoxin tolerant RAW264.7 cells.

Conclusion: In in vitro endotoxin tolerant macrophages, the expression of Gfi1 mRNA and protein were up-regulated after high dose LPS stimulation, accompanied with a blunted TNF-alpha and IL-6 secretion. Gfi1 might participate in the mechanism of endotoxin tolerance.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / immunology*
  • Interleukin-6 / immunology
  • Interleukin-6 / metabolism*
  • Lipopolysaccharides / immunology
  • Lipopolysaccharides / pharmacology*
  • Macrophages* / cytology
  • Macrophages* / drug effects
  • Macrophages* / immunology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Transcription Factors / genetics
  • Transcription Factors / immunology*
  • Tumor Necrosis Factor-alpha / immunology
  • Tumor Necrosis Factor-alpha / metabolism*
  • Up-Regulation

Substances

  • DNA-Binding Proteins
  • Gfi1 protein, mouse
  • Interleukin-6
  • Lipopolysaccharides
  • Transcription Factors
  • Tumor Necrosis Factor-alpha