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receptor gene and sensitivity to
growth inhibition following polyamine depletion
Department of Surgery, University of Maryland School of Medicine and Baltimore Veterans Affairs Medical Center, Baltimore, Maryland 21201
Our previous studies
have shown that inhibition of polyamine biosynthesis increases the
sensitivity of intestinal epithelial cells to growth inhibition induced
by exogenous transforming growth factor-
(TGF-
). This study went
further to determine whether expression of the TGF-
receptor genes
is involved in this process. Studies were conducted in the IEC-6 cell
line, derived from rat small intestinal crypt cells. Administration of
-difluoromethylornithine (DFMO), a specific inhibitor of ornithine
decarboxylase (the rate-limiting enzyme for polyamine synthesis), for 4 and 6 days depleted cellular polyamines putrescine, spermidine, and
spermine in IEC-6 cells. Polyamine depletion by DFMO increased levels
of the TGF-
type I receptor (TGF-
RI) mRNA and protein but had no
effect on the TGF-
type II receptor expression. The induced
TGF-
RI expression after polyamine depletion was associated with an
increased sensitivity to growth inhibition induced by exogenous TGF-
but not by somatostatin. Extracellular matrix laminin inhibited IEC-6
cell growth without affecting the TGF-
receptor expression. Laminin
consistently failed to induce the sensitivity of TGF-
-mediated
growth inhibition. In addition, decreasing TGF-
RI expression by
treatment with retinoic acid not only decreased TGF-
-mediated growth
inhibition in normal cells but also prevented the increased sensitivity
to exogenous TGF-
in polyamine-deficient cells. These results
indicate that 1) depletion of cellular polyamines by DFMO
increases expression of the TGF-
RI gene and 2) increased
TGF-
RI expression plays an important role in the process through
which polyamine depletion sensitizes intestinal epithelial cells to
growth inhibition induced by TGF-
.
cell proliferation; transforming growth factor-
receptor; laminin; retinoic acid; IEC-6
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