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Get Free AccessIntestinal epithelial cells (IECs) are capable of mounting an adequate antimicrobial inflammatory response to pathogens while tolerating commensals. The underlying regulatory mechanisms of immune sensitivity remain incompletely understood, particularly in the context of human IECs. To enhance our understanding of the immune response of IECs to bacterial epithelial barrier breach, we investigated whether epithelial responsiveness is contingent on cell identity and cell polarization. We exposed human intestinal organoids to bacterial antigens to study their immune responses. Notable discrepancies were observed in the specific reactions exhibited by intestinal stem cells (ISCs) and enterocytes. It was determined that basolateral exposure of IECs to bacterial antigens resulted in a robust response, whereas apical exposure elicited a significantly more modest response. We identified ISCs as the responders, while the reaction of enterocytes was found to be attenuated. The regulation of bacterial responsiveness in enterocytes occurs at multiple levels, including the modulation of NFκB activation and post-transcriptional control of mRNA stability. Our findings demonstrate that differentiated non-responsive enterocytes can be sensitized to bacterial antigens through the activation of the WNT pathway. These findings extend the crucial role of WNT signaling for intestinal epithelial homeostasis and regulation of stem cell maintenance, proliferation, differentiation, and tissue architecture in the gut. Additionally, they reveal a new function of WNT signaling in regulating microbial responses within the intestinal environment.
Maaike Hillegonda de Vries, Claartje Meddens, Hemme Hijma, Anne‐Claire Berrens, Suze A. Jansen, Berend A. P. Kooiman, Scott B Snapper, Hans Clevers, Michal Mokrý, Ewart Kuijk, Edward E. S. Nieuwenhuis (2025). Human colon stem cells are the principal epithelial responders to bacterial antigens. , DOI: https://doi.org/10.1101/2025.02.07.637053.
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Type
Preprint
Year
2025
Authors
11
Datasets
0
Total Files
0
Language
en
DOI
https://doi.org/10.1101/2025.02.07.637053
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