Hepatic stellate cells' involvement in progenitor-mediated liver regeneration

Lab Invest. 2010 Aug;90(8):1199-208. doi: 10.1038/labinvest.2010.88. Epub 2010 May 3.

Abstract

Earlier studies conducted by our laboratory have shown that suppression of transforming growth factor-beta (TGFbeta)-mediated upregulation of connective tissue growth factor (CTGF) by iloprost resulted in a greatly diminished oval cell response to 2-acetylaminofluorene/partial hepatectomy (2AAF/PH) in rats. We hypothesized that this effect is due to decreased activation of hepatic stellate cells. To test this hypothesis, we maintained rats on a diet supplemented with 2% L-cysteine as a means of inhibiting stellate cell activation during the oval cell response to 2AAF/PH. In vitro experiments show that L-cysteine did, indeed, prevent the activation of stellate cells while exerting no direct effect on oval cells. Desmin immunostaining of liver sections from 2AAF/PH animals indicated that maintenance on the L-cysteine diet resulted in an 11.1-fold decrease in the number of activated stellate cells within the periportal zones. The total number of cells proliferating in the periportal zones of livers from animals treated with L-cysteine was drastically reduced. Further analyses showed a greater than fourfold decrease in the magnitude of the oval cell response in animals maintained on the L-cysteine diet as determined by immunostaining for both OV6 and alpha-fetoprotein (AFP). Global liver expression of AFP as measured by real-time PCR was shown to be decreased 4.7-fold in the L-cysteine-treated animals. These data indicate that the activation of hepatic stellate cells is required for an appropriate oval cell response to 2AAF/PH.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • 2-Acetylaminofluorene / metabolism
  • 2-Acetylaminofluorene / pharmacology
  • Animals
  • Connective Tissue Growth Factor
  • Cysteine / metabolism
  • Cysteine / pharmacology
  • Hepatectomy
  • Hepatic Stellate Cells / physiology*
  • Liver / cytology
  • Liver / drug effects
  • Liver / metabolism
  • Liver Diseases / metabolism
  • Liver Regeneration / drug effects
  • Liver Regeneration / physiology*
  • Male
  • Rats
  • Rats, Inbred F344
  • Stem Cells / metabolism*
  • Transforming Growth Factor beta / metabolism
  • Transforming Growth Factor beta / pharmacology
  • alpha-Fetoproteins / metabolism
  • alpha-Fetoproteins / pharmacology

Substances

  • Transforming Growth Factor beta
  • alpha-Fetoproteins
  • Connective Tissue Growth Factor
  • 2-Acetylaminofluorene
  • Cysteine