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Gastrointestinal Unit and Center for the Study of Inflammatory Bowel Disease, Department of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts 02114-2696
Intestinal
epithelial cells may be actively involved in the immunoregulatory
pathways leading to intestinal inflammation. The aim of this study was
to assess expression by intestinal epithelial cells of cytokines with
potential involvement in the development of intestinal inflammation in
interleukin (IL)-2-deficient [(
/
)] mice.
Wild-type mice, mice heterozygous for the disrupted IL-2 gene, and
IL-2(
/
) mice were studied at 6, 16, and 24 wk of age. The
mRNA levels of transforming growth factor-
1 (TGF-
1), tumor necrosis factor-
(TNF-
), IL-1
, IL-6, IL-15, KC,
JE, and CD14 in colonic and small intestinal epithelial
cells were assessed by Northern blot analysis. CD14 was also measured
by Western blotting and reverse transcriptase polymerase chain reaction
(RT-PCR). TGF-
1 mRNA was constitutively expressed in both colonic
and small intestinal epithelial cells with increased expression in the
colonic epithelium of colitic mice. CD14 was detected only in colonic epithelial cells, and mRNA levels increased severalfold in
IL-2(
/
) mice with colitis. Northern analysis demonstrated
increased levels of TGF-
1 and CD14 mRNA in colonic epithelial cells
of IL-2(
/
) mice before the development of signs of
colitis. CD14 mRNA and protein expression in the epithelial cells of
colitic mice were confirmed by RT-PCR and Western blot analysis of
isolated cells. In addition, IL-2(
/
) mice also expressed
increased levels of IL-15 mRNA in small intestinal and colonic
epithelial cells compared with heterozygous control mice. TNF-
,
IL-1
, IL-6, KC, and JE mRNAs were only detectable in colonic
epithelial cells of mice after the onset of colitis. Enhanced
expression of TGF-
1, IL-15, and CD14 by colonic epithelial cells may
play a role in the subsequent development of colitis in
IL-2(
/
) mice.
lipopolysaccharide; CD14; interleukin-15; transforming growth
factor-
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