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downregulates expression of
Na+/H+ exchangers NHE2 and NHE3 in rat
intestine and human Caco-2/bbe cells
The Martin Boyer Laboratories, University of Chicago, Chicago, Illinois 60637
Diarrhea associated with inflammatory bowel diseases has
traditionally been attributed to stimulated secretion. The purpose of
this study was to determine whether chronic stimulation of intestinal
mucosa by interferon-
(IFN-
) affects expression and function of
the apical membrane Na+/H+ exchangers NHE2 and
NHE3 in rat intestine and Caco-2/bbe (C2) cells. Confluent C2 cells
expressing NHE2 and NHE3 were treated with IFN-
for 2, 24, and
48 h. Adult rats were injected with IFN-
intraperitoneally for
12 and 48 h. NHE2 and NHE3 activities were measured by
unidirectional 22Na influx across C2 cells and in rat
brush-border membrane vesicles. NHE protein and mRNA were assessed by
Western and Northern blotting. IFN-
treatment of C2 monolayers
caused a >50% reduction in NHE2 and NHE3 activities and protein
expression. In rats, region-specific, time- and dose-dependent
reductions of NHE2 and NHE3 activities, protein expression, and mRNA
were observed after exposure to IFN-
. Chronic exposure of intestinal
epithelial cells to IFN-
results in selective downregulation of NHE2
and NHE3 expression and activity, a potential cause of
inflammation-associated diarrhea.
inflammatory bowel disease; inflammation; mucosa; sodium transport; sodium absorption; water and electrolyte transport; diarrhea; malabsorption; transporter; intestinal adaptation
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