Abstract
The homeostatic proliferation-differentiation gradient in the esophageal epithelium is perturbed under inflammatory disease conditions such as gastroesophageal reflux disease and eosinophilic esophagitis. Herein we describe the protocols for rapid generation (<14 days) and characterization of single-cell-derived, three-dimensional (3D) esophageal organoids from human subjects and mice with normal esophageal mucosa or inflammatory disease conditions. While 3D organoids recapitulate normal epithelial renewal, proliferation, and differentiation, non-cell autonomous reactive epithelial changes under inflammatory conditions are evaluated in the absence of the inflammatory milieu. Reactive epithelial changes are reconstituted upon exposure to exogenous recombinant cytokines. These changes are modulated pharmacologically or genetically ex vivo. Molecular, structural, and functional changes are characterized by morphology, flow cytometry, biochemistry, and gene expression analyses.
Original language | English |
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Article number | e106 |
Pages (from-to) | e106 |
Journal | Current Protocols in Stem Cell Biology |
Volume | 52 |
Issue number | 1 |
DOIs | |
State | Published - Feb 2020 |
Keywords
- Animals
- Biopsy
- Cryopreservation
- Eosinophilic Esophagitis/pathology
- Epithelial Cells/pathology
- Esophagus/pathology
- Homeostasis
- Humans
- Mice
- Models, Biological
- Organoids/pathology