Journal
HEPATOLOGY
Volume 36, Issue 1, Pages 49-54Publisher
WILEY-BLACKWELL
DOI: 10.1053/jhep.2002.34511
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Funding
- NIDDK NIH HHS [P30 DK 34989, DK 25636, DK 48823] Funding Source: Medline
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Ursodeoxycholic acid (UDCA) can protect hepatocytes from apoptosis induced by a variety of stimuli including anti-Fas antibody. However, in vivo the Fas receptor is activated by its natural ligand, Fas-L, whereas anti-Fas antibodies are not a physiologic stimulus. We therefore have assessed the anti-apoptotic effects of UDCA and other bile acids in a novel coculture model where apoptosis is induced in murine hepatocytes; by membrane-bound Fas-L expressing fibroblasts. Primary hepatocytes were cultured overnight on collagen-coated coverslips with increasing concentrations of different bile acids and overlaid with either NIH 3T3 Fas-L+ or Fas-L- expressing fibroblasts. After 6 hours cells were fixed and apoptosis was evaluated by TUNEL assay and DAPI staining using digital imaging. Fas-L protein expression and Fas trimerization were evaluated by Western blot analysis. FITC-UDCA and Mitotracker Red were used to evaluate UDCA localization with mitochondria. UDCA (up to 100 mumol/L, P <.0001), TUDCA (up to 400 mumol/L, P <.0001), and TCDCA (up to 200 mumol/L, P <.0001), but not TCA (up to 500 mumol/L), significantly protected hepatocytes in Fas-L+ cocultures. UDCA had no significant effect on hepatocytes in Fas-L- cocultures. TUDCA, 50 mumol/L (P <.001) and TCDCA up to 200 mumol/L (P <.0001) also reduced the hepatocytes apoptotic rate in Fas-L- cocultures. Bile acids did not affect Fas-L expression in fibroblasts or Fas trimerization. FITC-UDCA colocalized with the mitochondrial probe. In conclusion, UDCA, TUDCA, and TCDCA but not TCA are capable of protecting hepatocytes from Fas-L-induced apoptosis. This protective effect is not associated with reductions in Fas trimerization, but may be related to a direct effect on the mitochondrial membrane.
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