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LIVER AND BILIARY TRACT
-dependent mechanism in human cholangiocyte cell lines
Division of Gastroenterology and Hepatology, Mayo Medical School, Clinic, and Foundation, Rochester, Minnesota 55905
Submitted 20 December 2002 ; accepted in final form 21 February 2003
Bile acids transactivate the EGF receptor (EGFR) in cholangiocytes.
However, the mechanisms by which bile acids transactivate the EGFR remain
unknown. Our aims were to examine the effects of bile acids on EGFR activation
in human cholangiocyte cell lines KMBC and H-69. Bile acids stimulated cell
growth and induced EGFR phosphorylation in a ligand-dependent manner. Although
cells constitutively expressed several EGFR ligands, only transforming growth
factor-
(TGF-
) antisera effectively blocked bile acid-induced
EGFR phosphorylation. Consistent with the concept that matrix
metalloproteinase (MMP) activity is requisite for TGF-
membrane release
and ligand function, bile acid transactivation of EGFR and cell growth was
blocked by an MMP inhibitor. In conclusion, bile acids activate EGFR via a
TGF-
-dependent mechanism, and this EGFR activation promotes cellular
growth.
c-Src kinase; matrix metalloproteinase; ligand dependent; transactivation
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