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a Department of
Gastroenterology, Hepatology, and Infectious Diseases,
Otto-von-Guericke University Magdeburg, D-39120 Magdeburg, Germany, b Institute of Pathology, Otto-von-Guericke
University Magdeburg, D-39120 Magdeburg,
Germany, c Institute of Molecular Biology and Medical
Chemistry, Otto-von-Guericke University Magdeburg, D-39120 Magdeburg,
Germany, d Department
of General Surgery, Otto-von-Guericke University Magdeburg, D-39120
Magdeburg, Germany, e Department of Gastroenterology, University of
Ulm, D-89075 Ulm, Germany
Correspondence to: Dr M P A Ebert, Department of Gastroenterology, Hepatology and Infectious Diseases, Otto-von-Guericke University Magdeburg, Leipzigerstrasse 44, D-39120 Magdeburg, Germany.
Accepted for publication 2 February 1999
BACKGROUND/AIMS
Chronic
pancreatitis is an inflammatory disease of the exocrine pancreas
associated with extensive fibrosis, enlarged pancreatic ducts, acinar
cell degeneration, and the formation of tubular complexes. The
molecular and biochemical alterations associated with these
histological changes are not kown. Generally, the new family of TFF
peptides (formerly known as P-domain peptides or trefoil factors) is
aberrantly expressed during chronic inflammatory diseases of the
gastrointestinal tract.
METHODS
Using human
pancreatic tissues obtained from patients with chronic pancreatitis and
murine pancreatic tissues obtained from transgenic mice overexpressing
transforming growth factor
(TGF-
), the expression and cellular
distribution of TFF1 was analysed using northern blot analysis,
polymerase chain reaction (PCR), and immunohistochemistry.
RESULTS
In the
normal human pancreas, TFF1 was scarce, with only a few ducts
exhibiting cytoplasmic TFF1 immunoreactivity. In contrast, human
chronic pancreatitis tissue specimens exhibited strong TFF1 immunoreactivity in ductal cells, areas of ductal hyperplasia, and
tubular complexes. Semiquantitative PCR analysis of TFF1 mRNA levels
showed enhanced expression of TFF1 in the pancreas of patients with
chronic pancreatitis. Furthermore, TFF1 mRNA levels were detectable in
the pancreas in four of five transgenic mice overexpressing TGF-
. In
contrast, four of five wild type mice did not exhibit a TFF1 mRNA
transcript. In addition, while no specific TFF1 immunoreactivity was
present in the pancreas of the wild type mice, ductal epithelial cells
and duct-like tubular complexes in the pancreas of the transgenic mice
overexpressing TGF-
exhibited pronounced TFF1 immunoreactivity.
CONCLUSIONS
Ductal
cells and tubular complexes in pancreatic fibrosis express TFF1. As the
5'-flanking region of TFF1 contains an epidermal growth factor
responsive enhancer region and the expression of epidermal growth
factor and TGF-
is enhanced in pancreatic fibrosis, the enhanced
expression of TFF1 in pancreatic fibrosis may be mediated by TGF-
.
;
TFF peptides
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