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A subpopulation of mouse esophageal basal cells has properties of stem cells with the capacity for self-renewal and lineage specification
Jiri Kalabis, … , Meenhard Herlyn, Anil K. Rustgi
Jiri Kalabis, … , Meenhard Herlyn, Anil K. Rustgi
Published November 6, 2008
Citation Information: J Clin Invest. 2008;118(12):3860-3869. https://doi.org/10.1172/JCI35012.
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Research Article

A subpopulation of mouse esophageal basal cells has properties of stem cells with the capacity for self-renewal and lineage specification

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Abstract

The esophageal epithelium is a prototypical stratified squamous epithelium that exhibits an exquisite equilibrium between proliferation and differentiation. After basal cells proliferate, they migrate outward toward the luminal surface, undergo differentiation, and eventually slough due to apoptosis. The identification and characterization of stem cells responsible for the maintenance of the esophageal epithelium remains elusive. Here, we employed Hoechst dye extrusion and BrdU label–retaining assays to identify in mice a potential esophageal stem cell population that localizes to the basal cell compartment. The self-renewing capacity of this population was characterized using a clonogenic assay and a 3D organotypic culture model. The putative esophageal stem cells were also capable of epithelial reconstitution in vivo in direct esophageal epithelial injury models. In both the 3D organotypic culture and direct mucosal injury models, the putative stem cells gave rise to undifferentiated and differentiated cells. These studies therefore provide a basis for understanding the regenerative capacity and biology of the esophageal epithelium when it is faced with injurious insults.

Authors

Jiri Kalabis, Kenji Oyama, Takaomi Okawa, Hiroshi Nakagawa, Carmen Z. Michaylira, Douglas B. Stairs, Jose-Luiz Figueiredo, Umar Mahmood, J. Alan Diehl, Meenhard Herlyn, Anil K. Rustgi

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Figure 5

SP cells are able to differentiate in organotypic culture, giving rise to proliferative basal CK14+CK13–CK4– and differentiated suprabasal CK14–CK13+CK4+ cells.

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SP cells are able to differentiate in organotypic culture, giving rise t...
(A–C) Unsorted freshly isolated WT (GFP–) cells did not form an epithelium layer (similar to data shown in Figure 4) with immunohistochemical staining for (A) CK14, (B) CK4, and (C) CK13. (D–F) Sorted 103 NSP cells from GFP+ mice mixed with 3 × 104 unsorted GFP– cells did not form an epithelium (similar to data shown in Figure 4) with immunohistochemical staining for (D) CK14, (E) CK4, and (F) CK13. (G–I) SP cells (103) from GFP+ mice mixed with 3 × 104 unsorted GFP– cells formed a complete epithelium with luminal keratinization (similar to data shown in Figure 4) with well-defined proliferative basal and differentiated suprabasal cells. Immunohistochemical staining for (G) CK14, (H) CK4, and (I) CK13. Dashed lines indicate the basement membrane. Original magnification, ×400. Scale bar: 25 μm.

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