Chitotriosidase gene expression in Kupffer cells from patients with non-alcoholic fatty liver disease

Gut. 2006 Sep;55(9):1313-20. doi: 10.1136/gut.2005.075697. Epub 2006 Jul 6.

Abstract

Background and aims: Non-alcoholic steatohepatitis (NASH) is a clinicopathological condition characterised by a necroinflammatory disorder with fatty infiltration of the hepatocytes. The molecular mechanisms involved in the anomalous behaviour of liver cells have only partially been determined. Human chitotriosidase (Chit) is a chitinolytic enzyme mainly produced by activated macrophages. The aim of this study was to investigate the expression of the chitinase-like gene in Kupffer cells, to determine how chitotriosidase may be implicated in the progression from uncomplicated steatosis to steatohepatitis with progressive fibrosis.

Methods: 75 subjects were studied: 40 with NASH, 20 with simple steatosis, and 15 normal controls. Kupffer cells obtained from liver biopsies were used to detect CHIT expression, superoxide anion (O2-), lipid peroxidation, and tumour necrosis factor alpha (TNFalpha) and ferritin levels.

Results: CHIT expression differed markedly in livers from normal controls and in those from patients with simple steatosis or non-alcoholic steatohepatitis. A significant correlation between mRNA CHIT and O2-, lipid peroxidation, TNFalpha, and ferritin levels was observed in both NASH and simple steatosis.

Conclusions: Human Kupffer cells in NASH patients overproduce chitotriosidase. At the highest levels of production, this enzyme may play a role in increasing the risk for a poor outcome in steatohepatitis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Disease Progression
  • Fatty Liver / enzymology*
  • Fatty Liver / metabolism
  • Female
  • Ferritins / metabolism
  • Gene Expression
  • Hexosaminidases / biosynthesis*
  • Hexosaminidases / genetics
  • Humans
  • Kupffer Cells / enzymology*
  • Kupffer Cells / metabolism
  • Lipid Peroxidation
  • Male
  • Middle Aged
  • Polymerase Chain Reaction / methods
  • RNA, Messenger / genetics
  • Superoxides / metabolism
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • Superoxides
  • Ferritins
  • Hexosaminidases
  • chitotriosidase