Cellular Heterogeneity in the Mouse Esophagus Implicates the Presence of a Nonquiescent Epithelial Stem Cell Population

Because the esophageal epithelium lacks a defined stem cell niche, it is unclear whether all basal epithelial cells in the adult esophagus are functionally equivalent. In this study, we showed that basal cells in the mouse esophagus contained a heterogeneous population of epithelial cells, similar t...

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Main Authors: Aaron D. DeWard, Julie Cramer, Eric Lagasse
Format: Article
Language:English
Published: Elsevier 2014-10-01
Series:Cell Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124714008109
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spelling doaj-41d8305a68cb455f8b3e7364247067b62020-11-25T01:17:53ZengElsevierCell Reports2211-12472014-10-019270171110.1016/j.celrep.2014.09.027Cellular Heterogeneity in the Mouse Esophagus Implicates the Presence of a Nonquiescent Epithelial Stem Cell PopulationAaron D. DeWard0Julie Cramer1Eric Lagasse2Department of Pathology, University of Pittsburgh, Pittsburgh, PA 15219, USADepartment of Pathology, University of Pittsburgh, Pittsburgh, PA 15219, USADepartment of Pathology, University of Pittsburgh, Pittsburgh, PA 15219, USABecause the esophageal epithelium lacks a defined stem cell niche, it is unclear whether all basal epithelial cells in the adult esophagus are functionally equivalent. In this study, we showed that basal cells in the mouse esophagus contained a heterogeneous population of epithelial cells, similar to other rapidly cycling tissues such as the intestine or skin. Using a combination of cell-surface markers, we separated primary esophageal tissue into distinct cell populations that harbored differences in stem cell potential. We also used an in vitro 3D organoid assay to demonstrate that Sox2, Wnt, and bone morphogenetic protein signaling regulate esophageal self-renewal. Finally, we labeled proliferating basal epithelial cells in vivo to show differing cell-cycle profiles and proliferation kinetics. Based on our results, we propose that a nonquiescent stem cell population resides in the basal epithelium of the mouse esophagus.http://www.sciencedirect.com/science/article/pii/S2211124714008109
collection DOAJ
language English
format Article
sources DOAJ
author Aaron D. DeWard
Julie Cramer
Eric Lagasse
spellingShingle Aaron D. DeWard
Julie Cramer
Eric Lagasse
Cellular Heterogeneity in the Mouse Esophagus Implicates the Presence of a Nonquiescent Epithelial Stem Cell Population
Cell Reports
author_facet Aaron D. DeWard
Julie Cramer
Eric Lagasse
author_sort Aaron D. DeWard
title Cellular Heterogeneity in the Mouse Esophagus Implicates the Presence of a Nonquiescent Epithelial Stem Cell Population
title_short Cellular Heterogeneity in the Mouse Esophagus Implicates the Presence of a Nonquiescent Epithelial Stem Cell Population
title_full Cellular Heterogeneity in the Mouse Esophagus Implicates the Presence of a Nonquiescent Epithelial Stem Cell Population
title_fullStr Cellular Heterogeneity in the Mouse Esophagus Implicates the Presence of a Nonquiescent Epithelial Stem Cell Population
title_full_unstemmed Cellular Heterogeneity in the Mouse Esophagus Implicates the Presence of a Nonquiescent Epithelial Stem Cell Population
title_sort cellular heterogeneity in the mouse esophagus implicates the presence of a nonquiescent epithelial stem cell population
publisher Elsevier
series Cell Reports
issn 2211-1247
publishDate 2014-10-01
description Because the esophageal epithelium lacks a defined stem cell niche, it is unclear whether all basal epithelial cells in the adult esophagus are functionally equivalent. In this study, we showed that basal cells in the mouse esophagus contained a heterogeneous population of epithelial cells, similar to other rapidly cycling tissues such as the intestine or skin. Using a combination of cell-surface markers, we separated primary esophageal tissue into distinct cell populations that harbored differences in stem cell potential. We also used an in vitro 3D organoid assay to demonstrate that Sox2, Wnt, and bone morphogenetic protein signaling regulate esophageal self-renewal. Finally, we labeled proliferating basal epithelial cells in vivo to show differing cell-cycle profiles and proliferation kinetics. Based on our results, we propose that a nonquiescent stem cell population resides in the basal epithelium of the mouse esophagus.
url http://www.sciencedirect.com/science/article/pii/S2211124714008109
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