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Enteroids expressing a disease-associated mutant of EpCAM are a model for congenital tufting enteropathy.

Barun Das,Kevin Okamoto,J. Rabalais,P. Kozan,R. Marchelletta,Matthew D. McGeough,Nassim Durali,Maria Go,K. Barrett,Soumita Das,Mamata Sivagnanam

Published 2019 in American Journal of Physiology - Gastrointestinal and Liver Physiology

ABSTRACT

Congenital Tufting Enteropathy (CTE) is an autosomal recessive disease characterized by severe intestinal failure in infancy and mutations in the epithelial cell adhesion molecule (EPCAM) gene. Previous studies of CTE in mice expressing mutant EpCAM show neonatal lethality. Hence, to study the cellular, molecular, and physiological alterations that result from EpCAM mutation, a tamoxifen-inducible mutant EpCAMenteroid model has been generated. The presence of mutant EpCAM in the model was confirmed at both mRNA and protein levels. Immunofluorescence microscopy demonstrated the reduced expression of mutant EpCAM. Mutant enteroids had reduced budding potential as well as significantly decreased mRNA expression for epithelial lineage markers (Mucin 2, Lysozyme, Sucrase-Isomaltase), proliferation marker Ki67 and secretory pathway transcription factors (Atoh1, Hnf1b). Significantly decreased numbers of Paneth and goblet cells were confirmed by staining. These findings were correlated with intestinal tissue from CTE patients and the mutant mice model that had significantly fewer Paneth and goblet cells than in healthy counterparts. FITC-dextran studies demonstrated significantly impaired barrier function in monolayers derived from mutant enteroids compared to control monolayers. In conclusion, we have established an ex vivo CTE model. The role of EpCAM in the budding potential, differentiation, and barrier function of enteroids is noted. Our study establishes new facets of EpCAM biology that will aid in understanding the pathophysiology of CTE and the role of EpCAM in health and disease.

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