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Am J Physiol Gastrointest Liver Physiol 285: G31-G36, 2003. First published February 26, 2003; doi:10.1152/ajpgi.00536.2002
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LIVER AND BILIARY TRACT

Bile acids activate EGF receptor via a TGF-{alpha}-dependent mechanism in human cholangiocyte cell lines

Nathan W. Werneburg, Jung-Hwan Yoon, Hajime Higuchi, and Gregory J. Gores

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-{alpha} (TGF-{alpha}) antisera effectively blocked bile acid-induced EGFR phosphorylation. Consistent with the concept that matrix metalloproteinase (MMP) activity is requisite for TGF-{alpha} 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-{alpha}-dependent mechanism, and this EGFR activation promotes cellular growth.

c-Src kinase; matrix metalloproteinase; ligand dependent; transactivation



Address for reprint requests and other correspondence: G. J. Gores, Professor of Medicine, Mayo Medical School, Clinic, and Foundation, 200 First St. SW, Rochester, MN 55905 (E-mail: gores.gregory{at}mayo.edu).




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