201. Interleukin-13 and transforming growth factor β synergise in the pathogenesis of human intestinal fistulae.
- Author
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Scharl M, Frei S, Pesch T, Kellermeier S, Arikkat J, Frei P, Fried M, Weber A, Jehle E, Rühl A, and Rogler G
- Subjects
- Adult, Biomarkers metabolism, Blotting, Western, Case-Control Studies, Colitis, Ulcerative metabolism, Crohn Disease metabolism, Crohn Disease pathology, Female, Fibroblasts metabolism, Fibroblasts pathology, HT29 Cells, Humans, Integrin beta Chains metabolism, Intestinal Fistula metabolism, Intestinal Fistula pathology, Intestinal Mucosa pathology, Male, Middle Aged, Real-Time Polymerase Chain Reaction, Snail Family Transcription Factors, Transcription Factors metabolism, Crohn Disease complications, Interleukin-13 metabolism, Intestinal Fistula etiology, Intestinal Mucosa metabolism, Transforming Growth Factor beta metabolism
- Abstract
Objective: Epithelial to mesenchymal transition (EMT) seems to play an important role in the pathogenesis of fistulae, a common clinical complication of Crohn's disease (CD). TGFβ and interleukin-13 (IL-13) have been correlated with the onset of EMT-associated organ fibrosis and high levels of TGFβ have been shown in transitional cells (TCs) lining CD fistula tracts. This study investigated whether IL-13 could be involved in the pathogenesis of CD-associated fistulae., Design: Protein or mRNA levels in HT29 intestinal epithelial cells (IECs) or colonic lamina propria fibroblasts (CLPFs) were studied by western blotting or real-time PCR. CLPFs were isolated from non-inflammatory disease controls or patients with CD with or without fistulae and IL-13 levels were analysed in surgically removed fistula specimens by immunohistochemistry., Results: TGFβ induced IL-13 secretion in CLPFs from patients with fistulising CD. In fistula specimens high levels of IL-13 were detected in TCs covering fistula tracts. In HT29 IEC monolayers, IL-13 induced SLUG and β6-integrin mRNA, which are associated with cell invasion. HT29 spheroids completely disintegrated when treated with TGFβ for 7 days, whereas IL-13-treated spheroids did not show morphological changes. Here, TGFβ induced mRNA expression of SNAIL1 and IL-13, whereas IL-13 elevated SLUG and β6-integrin mRNA. An anti-IL-13 antibody was able to prevent IL-13-induced SLUG expression in HT29 IECs., Conclusions: TGFβ induces IL-13 expression and an EMT-like phenotype of IECs, while IL-13 promotes the expression of genes associated with cell invasion. These findings suggest that TGFβ and IL-13 play a synergistic role in the pathogenesis of fistulae and inhibition of IL-13 might represent a novel therapeutic approach for fistula treatment.
- Published
- 2013
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