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Updated: Mar 8, 2026

Induced Differentiation of M Cell-like Cells in Human Stem Cell-derived Ileal Enteroid Monolayers
Published on: July 26, 2019
The effect of polymeric formula on enterocyte differentiation
Gabrielle R Budd1, Alan Aitchison1, Andrew S Day2
11 Department of Surgery, University of Otago Christchurch, Christchurch, New Zealand.
Insights
Exclusive enteral nutrition, a therapy for Crohn's disease (CD), may work by increasing intestinal alkaline phosphatase (IAP). This enzyme strengthens the gut's innate immune response to bacteria, potentially aiding CD remission.
Area of Science:
- Gastroenterology
- Immunology
- Cell Biology
Background:
- Exclusive enteral nutrition (EEN) is a primary treatment for active Crohn's disease (CD), particularly in pediatric patients.
- The precise mechanisms underlying EEN's therapeutic effects in CD remain incompletely understood.
- Intestinal alkaline phosphatase (IAP) is a known marker of enterocyte differentiation and plays a role in the gut's innate immunity.
Purpose of the Study:
- To investigate the effect of polymeric formula (PF) on intestinal alkaline phosphatase (IAP) expression in intestinal cells.
- To explore potential mechanisms by which EEN might modulate the gut's immune response in the context of Crohn's disease.
Main Methods:
- Utilized the Caco-2 human adenocarcinoma cell line.
- Incubated Caco-2 cells with a polymeric formula (PF).
- Quantified the expression of cell surface-associated intestinal alkaline phosphatase (IAP).
Main Results:
- Incubation with polymeric formula (PF) led to a dose-dependent increase in cell surface IAP expression.
- This suggests PF influences IAP levels in intestinal cells.
- The findings indicate a potential role for IAP modulation in EEN's efficacy.
Conclusions:
- Cell surface-associated IAP expression is enhanced by polymeric formula (PF) in vitro.
- This enhancement may represent a mechanism by which EEN strengthens the gut's innate immune response.
- Further research is needed to elucidate the specific pathways involved and confirm these findings in vivo for Crohn's disease patients.
Abstract:
Exclusive enteral nutrition is established as an initial therapy to induce remission in active Crohn's disease (CD), especially in children, but the mechanisms of action of this therapy are yet to be fully defined. Intestinal alkaline phosphatase (IAP), a recognised marker of enterocyte differentiation, is implicated in the innate gut immune response to enteric pathogens. Using the Caco-2 human adenocarcinoma cell line, this study showed that the incubation of human cells with a polymeric formula (PF) resulted in a dose-dependent increase in the expression of IAP on the cell surface. While further investigation is required to determine the pathway(s) involved, this finding suggests that cell surface-associated IAP may be an aspect of the gut's innate immune response to pathogenic bacteria that is strengthened by PF in the setting of CD.
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