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gene during
growth inhibition following polyamine depletion
Department of Surgery, University of Maryland Medical School and Baltimore Veterans Affairs Medical Center, Baltimore, Maryland 21201
Polyamine depletion and cytokine transforming growth factor-
(TGF-
) inhibit cell proliferation. The current study tests the
hypothesis that polyamine depletion results in growth inhibition by
altering expression of the TGF-
gene in intestinal epithelial cells.
Studies were conducted in the IEC-6 cell line derived from rat small
intestinal crypt cells. Cells were grown in DMEM in the presence or
absence of
-difluoromethylornithine (DFMO), a specific inhibitor of
polyamine biosynthesis, for 6 and 12 days. Administration of DFMO not
only depleted intracellular polyamines but also significantly increased
the mRNA levels of TGF-
. Increased TGF-
mRNA in DFMO-treated
cells was paralleled by an increase in TGF-
content. Depletion of
intracellular polyamines by DFMO had no effect on the rate of TGF-
gene transcription, as measured by nuclear run-on assay. The half-life
of mRNA for TGF-
in normal cells was ~65 min and increased to
>16 h in cells treated with DFMO for 6 or 12 days. Exogenous
polyamine, when given together with DFMO, prevented the increased
half-life of TGF-
mRNA in IEC-6 cells. TGF-
added to the culture
medium significantly decreased the rate of DNA synthesis and final cell
number in normal and polyamine-deficient cells. Furthermore, growth
inhibition caused by polyamine depletion was partially but
significantly blocked by addition of immunoneutralizing anti-TGF-
antibody. These results indicate that
1) depletion of intracellular
polyamines induces the activation of the TGF-
gene through
posttranscriptional regulation and
2) increased expression of the
TGF-
gene plays an important role in the process of growth
inhibition following polyamine depletion.
cell proliferation; intestinal crypt; posttranscription; ornithine decarboxylase
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