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J Infect Dis ; 189(11): 2110-9, 2004 Jun 01.
Article in English | MEDLINE | ID: mdl-15143480

ABSTRACT

BACKGROUND: Presentation after Clostridium difficile infection may depend on the level of epithelial exposure to toxins. We investigated epithelial barrier function and expression of interleukin (IL)-8 and transforming growth factor (TGF)-beta in response to varying concentrations of C. difficile toxin A. METHODS: T84 cells were either preexposed or continuously exposed to C. difficile toxin A (0.01-1000 ng/mL). Barrier function was assessed by measurements of transepithelial electrical resistance. RESULTS: Preexposure to < or =10 ng/mL toxin A led to an increase in the release of TGF-beta 1, but there was no change in the expression of IL-8. In contrast, after preexposure to >10 ng/mL toxin A, there was enhanced expression of IL-8, but release of TGF-beta 1 was similar to that in control monolayers. After preexposure to >10 ng/mL toxin A, there was complete and irreversible loss of electrical resistance. At lower concentrations, loss of resistance across monolayers was followed by recovery, which was enhanced by all 3 recombinant isoforms of TGF-beta. Pretreatment with recombinant isoforms of TGF-beta or coculture with TGF-beta 3-expressing colonic subepithelial myofibroblasts was also protective. CONCLUSIONS: In C. difficile infection, the development and severity of colonic inflammation may depend on the exposure of intestinal epithelial cells to toxins and the expression of proinflammatory (IL-8) and protective (TGF-beta) factors.


Subject(s)
Bacterial Toxins/pharmacology , Clostridioides difficile/chemistry , Enterotoxins/pharmacology , Interleukin-8/biosynthesis , Intestinal Mucosa/drug effects , Transforming Growth Factor beta/biosynthesis , Biological Assay , Coculture Techniques , Electric Impedance , Enzyme-Linked Immunosorbent Assay , Epithelial Cells/drug effects , Epithelial Cells/metabolism , Fibroblasts , Humans , Interleukin-8/metabolism , Intestinal Mucosa/cytology , Intestinal Mucosa/metabolism , Protein Isoforms , Transforming Growth Factor beta/metabolism
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