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Am J Physiol Gastrointest Liver Physiol 288: G696-G704, 2005. First published November 4, 2004; doi:10.1152/ajpgi.00206.2004
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MUCOSAL BIOLOGY

Luminal bacterial flora determines physiological expression of intestinal epithelial cytoprotective heat shock proteins 25 and 72

Donna L. Arvans,1 Stephan R. Vavricka,1 Hongyu Ren,1 Mark W. Musch,1 Lisa Kang,1 Flavio G. Rocha,1 Alvaro Lucioni,1 Jerrold R. Turner,2 John Alverdy,3 and Eugene B. Chang1

1Department of Medicine, The Martin Boyer Laboratories, Inflammatory Bowel Research Center, and 2Departments of Pathology, and 3Surgery, University of Chicago, Chicago, Illinois

Submitted 5 May 2004 ; accepted in final form 28 October 2004

Heat shock proteins (HSP) 25 and 72 are expressed normally by surface colonocytes but not by small intestinal enterocytes. We hypothesized that luminal commensal microflora maintain the observed colonocyte HSP expression. The ability of the small intestine to respond to bacteria and their products and modulate HSPs has not been determined. The effects of luminal bacterial flora in surgically created midjejunal self-filling (SFL) vs. self-emptying (SEL) small-bowel blind loops on epithelial HSP expression were studied. HSP25 and HSP72 expression were assessed by immunoblot and immunohistochemistry. SFL were chronically colonized, whereas SEL contained levels of bacteria normal for the proximal small intestine. SFL creation significantly increased HSP25 and HSP72 expression relative to corresponding sections from SEL. Metronidazole treatment, which primarily affects anaerobic bacteria as well as a diet lacking fermentable fiber, significantly decreased SFL HSP expression. Small bowel incubation with butyrate ex vivo induced a sustained and significant upregulation of HSP25 and altered HSP72 expression, confirming the role of short-chain fatty acids. To determine whether HSPs induction altered responses to an injury, effects of the oxidant, monochloramine, on epithelial resistance and short-circuit current (Isc) responses to carbachol and glucose were compared. Increased SFL HSP expression was associated with protection against oxidant-induced decreases in transmural resistance and Isc responses to glucose, but not secretory responses to carbachol. In conclusion, luminal microflora and their metabolic byproducts direct expression of HSPs in gut epithelial cells, an effect that contributes to preservation of epithelial cell viability under conditions of stress.

enteric flora; metronidazole; butyrate; short-chain fatty acids; cytoprotection; host defense; intestinal flora; blind loop; stress; mucosal injury



Address for reprint requests and other correspondence: E. B. Chang, Martin Boyer Professor of Medicine, The Univ. of Chicago, 5841 S. Maryland Ave. Rm. G705, MC 6084, Chicago, IL, 60637 (E-mail: echang{at}medicine.bsd.uchicago.edu)




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