4.5 Article

A β-Glucan-Based Dietary Fiber Reduces Mast Cell-Induced Hyperpermeability in Ileum From Patients With Crohn's Disease and Control Subjects

Journal

INFLAMMATORY BOWEL DISEASES
Volume 24, Issue 1, Pages 166-178

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1093/ibd/izx002

Keywords

beta-glucan; Crohn's disease; intestinal permeability

Funding

  1. LIONS research foundation
  2. Swedish Foundation For Strategic Research [RB13-016]
  3. The Swedish Research Council (VR-Medicine and Health) [2014-02537]
  4. Swedish Research Council [2014-02537] Funding Source: Swedish Research Council

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Background: Administration of beta-glucan has shown immune-enhancing effects. Our aim was to investigate whether beta-glucan could attenuate mast cell (MC)-induced hyperpermeability in follicle-associated epithelium (FAE) and villus epithelium (VE) of patients with Crohn's disease (CD) and in noninflammatory bowel disease (IBD)-controls. Further, we studied mechanisms of beta-glucan uptake and effects on MCs in vitro. Methods: Segments of FAE and VE from 8 CD patients and 9 controls were mounted in Ussing chambers. Effects of the MC-degranulator compound 48/80 (C48/80) and yeast-derived beta-1,3/1,6 glucan on hyperpermeability were investigated. Translocation of beta-glucan and colocalization with immune cells were studied by immunofluorescence. Caco-2-cl1-and FAE-cultures were used to investigate beta-glucan-uptake using endocytosis inhibitors and HMC-1.1 to study effects on MCs. Results: beta-glucan significantly attenuated MC-induced paracellular hyperpermeability in CD and controls. Transcellular hyperpermeability was only significantly attenuated in VE. Baseline paracellular permeability was higher in FAE than VE in both groups, P<0.05, and exhibited a more pronounced effect by C48/80 and beta-glucan P<0.05. No difference was observed between CD and controls. In vitro studies showed increased passage, P<0.05, of beta-glucan through FAE-culture compared to Caco-2-cl1. Passage was mildly attenuated by the inhibitor methyl-beta-cyclodextrin. HMC-1.1 experiments showed a trend to decreasing MC-degranulation and levels of TNF-alpha but not IL-6 by beta-glucan. Immunofluorescence revealed more beta-glucan-uptake and higher percentage of macrophages and dendritic cells close to beta-glucan in VE of CD compared to controls. Conclusions: We demonstrated beneficial effects of beta-glucan on intestinal barrier function and increased beta-glucan-passage through FAE model. Our results provide important and novel knowledge on possible applications of beta-glucan in health disorders and diseases characterized by intestinal barrier dysfunction.

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