Deoxycholic acid activates the c-Jun N-terminal kinase pathway via FAS receptor activation in primary hepatocytes. Role of acidic sphingomyelinase-mediated ceramide generation in FAS receptor activation

J Biol Chem. 2004 Feb 13;279(7):5821-8. doi: 10.1074/jbc.M310979200. Epub 2003 Dec 2.

Abstract

We have shown previously that bile acids can activate the JNK pathway and down-regulate cholesterol 7alpha-hydroxylase (CYP7A1), the rate-limiting enzyme in the neutral pathway of bile acid biosynthesis. In this study, the mechanism(s) by which deoxycholic acid (DCA) activates the JNK pathway were examined. FAS receptor (FAS-R) and acidic sphingomyelinase (ASM)-deficient hepatocytes were resistant to DCA-induced activation of the JNK pathway. Activation of the JNK pathway (2-3-fold) in response to tumor necrosis factor-alpha was similar in both wild-type and FAS-R(-/-) hepatocytes. In wild-type and FAS-R(-/-) hepatocytes, ceramide elevation was detected as early as 2 min and peaked at 10 min after DCA treatment. In contrast, ASM(-/-) hepatocytes were defective in DCA-induced ceramide generation. Treatment with DCA resulted in movement of FAS-R to the cell surface, which was blocked upon treatment with brefeldin A. However, brefeldin A failed to block DCA-mediated JNK activation in wild-type hepatocytes. DCA-induced JNK activation was independent of either the epidermal growth factor receptor activation or free radical generation. Addition of ASM to rat hepatocytes activated JNK and down-regulated CYP7A1 mRNA levels. In conclusion, these results show that DCA activates JNK and represses CYP7A1 mRNA levels in primary hepatocytes via an ASM/FAS-R-dependent mechanism that is independent of either the epidermal growth factor receptor or free radical generation.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alleles
  • Animals
  • Bile Acids and Salts / metabolism
  • Brefeldin A / pharmacology
  • Cells, Cultured
  • Ceramides / metabolism
  • Cholesterol 7-alpha-Hydroxylase / biosynthesis
  • Cholesterol 7-alpha-Hydroxylase / metabolism
  • Deoxycholic Acid / metabolism*
  • Down-Regulation
  • Enzyme Activation
  • Enzyme Inhibitors / pharmacology
  • ErbB Receptors / metabolism
  • Free Radicals
  • Hepatocytes / metabolism*
  • JNK Mitogen-Activated Protein Kinases
  • Ligands
  • MAP Kinase Kinase 4
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mice, Transgenic
  • Microscopy, Fluorescence
  • Mitogen-Activated Protein Kinase Kinases / metabolism
  • Mitogen-Activated Protein Kinases / metabolism*
  • Protein-Tyrosine Kinases / antagonists & inhibitors
  • RNA, Messenger / metabolism
  • Rats
  • Sphingomyelin Phosphodiesterase / metabolism*
  • Time Factors
  • Tumor Necrosis Factor-alpha / metabolism
  • fas Receptor / metabolism*

Substances

  • Bile Acids and Salts
  • Ceramides
  • Enzyme Inhibitors
  • Free Radicals
  • Ligands
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • fas Receptor
  • Deoxycholic Acid
  • Brefeldin A
  • Cholesterol 7-alpha-Hydroxylase
  • ErbB Receptors
  • Protein-Tyrosine Kinases
  • JNK Mitogen-Activated Protein Kinases
  • Mitogen-Activated Protein Kinases
  • MAP Kinase Kinase 4
  • Mitogen-Activated Protein Kinase Kinases
  • Sphingomyelin Phosphodiesterase