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inhibits liver
collagen-
1(I) gene
expression through a tissue-specific regulatory region
Department of Medicine, Veterans Affairs Medical Center, and Center for Molecular Genetics, University of California, San Diego, California 92161
Although tumor
necrosis factor-
(TNF-
) inhibits
collagen-
1(I) gene expression
in cultured hepatic stellate cells, assessment of its effects on
hepatic collagen expression is complicated by the confounding variables
of tissue necrosis and inflammation. Therefore, we analyzed whether
chronically elevated serum TNF-
affects constitutive hepatic
collagen metabolism in vivo by inoculating nude mice with Chinese
hamster ovary (CHO) cells secreting TNF-
(TNF-
mice) or with
control CHO cells (control mice). Before the onset of weight loss,
collagen synthesis and collagen gene expression were inhibited in the
liver of TNF-
mice. In transgenic mice, after 8 h, TNF-
(500 ng
at 0 and 5 h) inhibited the liver expression of the
collagen-
1(I)-human growth
hormone (hGH) transgene containing the first intron and
440 bp
of the 5' region. Similarly, in cultured hepatic stellate cells
isolated from these transgenic animals, the
440 bp
collagen-
1(I)-hGH transgene was
responsive to TNF-
treatment independent of the activation of these
cells. Transfection studies in stellate cells allowed further
characterization of this TNF-
-responsive segment to
220 bp of
the 5' region. Because in the skin the inhibitory effect of
TNF-
involves a regulatory region of the
collagen-
1(I) gene beyond
440 bp, we herein identify a novel tissue-specific regulation of
collagen-
1(I) gene by TNF-
.
liver fibrosis; cytokines; cachexia; transcription; stellate cells
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