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Role of retinol in protecting epithelial cell damage induced by Clostridium difficile toxin A.

Authors :
Maciel AA
OriĆ” RB
Braga-Neto MB
Braga AB
Carvalho EB
Lucena HB
Brito GA
Guerrant RL
Lima AA
Source :
Toxicon : official journal of the International Society on Toxinology [Toxicon] 2007 Dec 15; Vol. 50 (8), pp. 1027-40. Date of Electronic Publication: 2007 Jul 31.
Publication Year :
2007

Abstract

Vitamin A (retinol), a fat-soluble vitamin, is an essential nutrient for the normal functioning of the visual system, epithelial cell integrity and growth, immunity, and reproduction. Our group has investigated the effect of high doses of oral vitamin A on early childhood diarrhea in our prospective community-based studies from Northeast Brazil and found a beneficial role in reducing the mean duration but not incidence of diarrheal episodes. In this study, we explored the role of retinol supplementation in intestinal cell lines following Clostridium difficile toxin A (TxA) challenge. C. difficile is the most common anaerobic pathogen borne with antibiotic-borne diarrhea and pseudomembranous colitis. Since retinol is critical for the integrity of tight junctions and to modulate the cell cycle, we have focused on changes in transepithelial electrical resistance (TEER) in Caco-2, a more differentiated intestinal cell line, and on models of cell proliferation, migration and viability in IEC-6 cells, an undifferentiated crypt cell line, following TxA injury. In this model, retinol therapy reduced apoptosis, improved cell migration and proliferation, and prevented the reduction in TEER, following C. difficile TxA challenge in a glutamine-free medium. These results suggest the role of retinol in protecting intestinal epithelial barrier function from C. difficile TxA enterotoxic damage.

Details

Language :
English
ISSN :
0041-0101
Volume :
50
Issue :
8
Database :
MEDLINE
Journal :
Toxicon : official journal of the International Society on Toxinology
Publication Type :
Academic Journal
Accession number :
17825865
Full Text :
https://doi.org/10.1016/j.toxicon.2007.07.010