Innate immune reactivity of the liver in rats fed a choline-deficient L-amino-acid-defined diet

World J Gastroenterol. 2008 Nov 21;14(43):6655-61. doi: 10.3748/wjg.14.6655.

Abstract

Aim: To investigate the innate immune reactivity of tumor necrosis factor-alpha (TNF-alpha), Toll-like receptor 4 (TLR4), and CD14 in the liver of non-alcoholic steatohepatitis (NASH) model rats.

Methods: Male F344 rats were fed a choline-deficient L-amino-acid-defined (CDAA) diet. The rats were killed after 4 or 8 wk of the diet, and their livers were removed for immunohistochemical investigation and RNA extraction. The liver specimens were immunostained for TNF-alpha, TLR4, and CD14. The gene expressions of TNF-alpha, TLR4, and CD14 were determined by reverse-transcriptase polymerase chain reaction (RT-PCR). Kupffer cells were isolated from the liver by Percoll gradient centrifugation, and were then cultured to measure TNF-alpha production.

Results: The serum and liver levels of TNF-alpha in the CDAA-fed rats increased significantly as compared with the control group, as did the immunohistochemical values and gene expressions of TNF-alpha, TLR4, and CD14 with the progression of steatohepatitis. TNF-alpha production from the isolated Kupffer cells of the CDAA-fed rats was elevated by lipopolysaccharide stimulation.

Conclusion: The expressions of TNF-alpha, TLR4, and CD14 increased in the NASH model, suggesting that TLR4 and CD14-mediated endotoxin liver damage may also occur in NASH.

MeSH terms

  • Alanine Transaminase / blood
  • Amino Acids / adverse effects*
  • Animals
  • Cells, Cultured
  • Choline Deficiency / complications*
  • Disease Models, Animal
  • Fatty Liver / etiology*
  • Fatty Liver / metabolism*
  • Fatty Liver / pathology
  • Immunity, Innate / physiology*
  • Kupffer Cells / metabolism
  • Kupffer Cells / pathology
  • Lipopolysaccharide Receptors / metabolism
  • Liver / metabolism*
  • Liver / pathology
  • Male
  • Rats
  • Rats, Inbred F344
  • Toll-Like Receptor 4 / metabolism
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Amino Acids
  • Lipopolysaccharide Receptors
  • Tlr4 protein, rat
  • Toll-Like Receptor 4
  • Tumor Necrosis Factor-alpha
  • Alanine Transaminase