Hepatic stellate cells primed with cytokines upregulate inflammation in response to peptidoglycan or lipoteichoic acid

Lab Invest. 2006 Jul;86(7):676-86. doi: 10.1038/labinvest.3700422. Epub 2006 Apr 17.

Abstract

Gram-positive bacterial products such as peptidoglycan (PGN) and lipoteichoic acid (LTA) are potent stimulators of innate inflammatory responses. We previously reported that lipopolysaccharide (LPS), a major biologically active agent of gram-negative bacteria, induces a proinflammatory response via the Toll-like receptor (TLR) 4 in hepatic stellate cells (HSCs). Here we investigated the mechanism of proinflammatory action by PGN and LTA in activated human HSCs. Following treatment with either TNF-alpha or IL-1beta, expression of TLR2 and CD14 was determined by real-time PCR and Western blotting. NF-kappaB activation was assessed by NF-kappaB-driven luciferase assay and electrophoretic mobility shift assay. Interleukin-8 (IL-8) from culture supernatant was measured by ELISA. Activated human HSCs express TLR2 and CD14, which are receptors for PGN and LTA signaling. TNF-alpha and IL-1beta significantly upregulated the expression of TLR2 mRNA and protein in HSCs. PGN and LTA induced NF-kappaB activation and stimulated production of IL-8 in HSCs. Pretreatment with TNF-alpha or IL-1beta augmented NF-kappaB activation and IL-8 production in response to PGN or LTA. Both PGN- and LTA-induced NF-kappaB activation and IL-8 secretion were completely inhibited by anti-TLR2 blocking antibody (T2.5). These findings suggest that TNF-alpha or IL-1beta primed HSCs enhance the production of IL-8 in response to PGN and LTA through augmentation of the TLR2 system.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenoviridae / genetics
  • Biomarkers / metabolism
  • Cell Culture Techniques
  • Cell Line, Transformed
  • Cytokines / immunology*
  • Fibrosis / chemically induced
  • Fibrosis / pathology
  • Genes, Reporter
  • Hepatocytes / cytology
  • Hepatocytes / physiology*
  • Humans
  • Inflammation / chemically induced
  • Inflammation / pathology
  • Interleukin-1 / immunology
  • Interleukin-8 / biosynthesis
  • Lipopolysaccharide Receptors / immunology
  • Lipopolysaccharides / immunology*
  • Liver / cytology*
  • Luciferases / immunology
  • NF-kappa B / immunology
  • Peptidoglycan / immunology*
  • Teichoic Acids / immunology*
  • Toll-Like Receptor 2 / immunology
  • Tumor Necrosis Factor-alpha / immunology
  • Up-Regulation / immunology

Substances

  • Biomarkers
  • Cytokines
  • Interleukin-1
  • Interleukin-8
  • Lipopolysaccharide Receptors
  • Lipopolysaccharides
  • NF-kappa B
  • Peptidoglycan
  • Teichoic Acids
  • Toll-Like Receptor 2
  • Tumor Necrosis Factor-alpha
  • lipoteichoic acid
  • Luciferases