4-Hydroxynonenal as a selective pro-fibrogenic stimulus for activated human hepatic stellate cells

J Hepatol. 2004 Jan;40(1):60-8. doi: 10.1016/s0168-8278(03)00480-x.


Background/aims: 4-Hydroxynonenal (HNE) is a putative pro-fibrogenic product of oxidative stress able to elicit apoptosis and cytotoxicity in several cell types. This study has been performed to evaluate its 'in vivo' levels in injured liver and whether HNE may induce apoptosis and/or affect selected phenotypic responses in activated human hepatic stellate cells (HSC/MF).

Methods/results: During the development of acute liver injury induced by CCl(4), liver tissue HNE levels were in the range 0.5-10 microM, as shown by high performance liquid chromatography analysis. Cultured human HSC/MF, developed cytotoxicity only if exposed to very high HNE concentrations (25-50 microM) without any sign of induction of classic, caspase-dependent apoptosis, as assessed by evaluating morphology and biochemical parameters of cell death. HNE, at non-cytotoxic doses, up-regulated procollagen type I and tissue inhibitor of metalloproteinases-1 gene expression and/or protein synthesis without significantly affecting chemotaxis (wound healing and haptotaxis assay), matrix metalloproteinases 1 and 2 mRNA expression and activity as well as basal DNA synthesis.

Conclusions: HNE, at concentrations compatible with those detected in vivo, does not elicit HSC/MF classic apoptosis but, rather, may act as a potent pro-fibrogenic stimulus for the expression of genes involved in excess extracellular matrix deposition and proposed as survival signals for HSC/MF.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism
  • Acute Disease
  • Aldehydes / administration & dosage
  • Aldehydes / metabolism
  • Aldehydes / pharmacology*
  • Animals
  • Apoptosis
  • Carbon Tetrachloride
  • Cell Death
  • Cells, Cultured
  • Chemical and Drug Induced Liver Injury
  • Cytoskeleton / drug effects
  • Dose-Response Relationship, Drug
  • Extracellular Matrix / genetics
  • Extracellular Matrix / metabolism
  • Gene Expression / drug effects
  • Humans
  • Liver / drug effects*
  • Liver / metabolism
  • Liver / pathology
  • Liver Cirrhosis / chemically induced*
  • Liver Cirrhosis / etiology
  • Liver Diseases / metabolism
  • Liver Diseases / pathology
  • Liver Diseases / physiopathology
  • Male
  • Osmolar Concentration
  • Phenotype
  • Rats
  • Rats, Wistar
  • Signal Transduction


  • Actins
  • Aldehydes
  • Carbon Tetrachloride
  • 4-hydroxy-2-nonenal