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Intestinal Disease Research Programme, Departments of 1 Medicine and 2 Pathology, McMaster University, Hamilton, Ontario, Canada L8N 3Z5
Specific in vivo T cell activation initiated by treatment with
anti-CD3 antibodies leads to diarrhea and structural damage of the
intestinal mucosa. In this study, the effect of T cell-induced mucosal
damage on jejunal epithelial ion transport, muscle contractility, and
neuronal ACh release was assessed in Ussing chambers, organ baths, and
a specialized perfusion apparatus, respectively. Time-matched control
mice received hamster serum containing irrelevant antibodies. Jejunal
segments from anti-CD3-treated mice displayed a significantly elevated
epithelial baseline short-circuit current (which indicates increased
ion transport) and a concomitant reduction in responsiveness to
prosecretory stimuli (nerve stimulation, carbachol, and forskolin). Longitudinal smooth muscle displayed altered spontaneous contractile activity, length-tension relationships, and carbachol-stimulated contraction in tissues excised from mice 20 and 40 h posttreatment. Anti-CD3 treatment did not affect stimulated ACh release from myenteric
plexus neurons. We conclude that specific T cell activation via
anti-CD3 antibody results in dramatic alterations in jejunal epithelial
and smooth muscle function. Such T cell-induced changes in intestinal
function may contribute to the symptomatology of T cell-mediated
enteropathies, including graft-versus-host disease, celiac disease, and
idiopathic inflammatory bowel disease.
epithelium; smooth muscle
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