Heliyon · 2022 · 23 citations · 49 references
Life SciencesBiochemistryImmunologyImmunopathologyInflammationMucosal ImmunologyDendritic Cell BiologyGastrointestinal ImmunologyGastrointestinal InflammationInflammatory Bowel DiseaseIntestinal Barrier FunctionMucosal Dendritic CellsDendritic Cell-mediated Mucosal ImmunityInflammation-induced Barrier DisruptionInflammatory Bowel Disease DysbiosisInflammatory Bowel Disease ImmunopathogenesisInflammatory Bowel Disease PathophysiologyInflammatory Bowel Disease-associated Dendritic CellsMucus Layer IntegritySecondary Bile Acids
human intestinal model to mimic chronic intestinal inflammation as seen during IBD. This model consisted of a co-culture of Caco-2 and HT29-MTX-E12 cells grown on a semi-wet interface with mechanical stimulation to represent the mucus layer. A pro-inflammatory environment was created by combining the co-culture with LPS-activated dendritic cells (DCs) in the basolateral compartment. The presence of activated DCs caused a decrease in transepithelial electrical resistance (TEER), which was slightly restored by LCA and sulfated DCA. The expression of genes related to intestinal epithelial integrity and the mucus layer were slightly, but not significantly increased. These results imply that sulfated BAs have a minor effect on intestinal barrier function in Caco-2 and HT29-MTX-E12 cells. When exposed directly to DCs, our results point towards anti-inflammatory effects of secondary BAs, but to a minor extent for sulfated secondary BAs. Future research should focus on the importance of proper transformation of BAs by bacterial enzymes and the potential involvement of BA dysmetabolism in IBD progression.
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