Long-lived keratin 15+ esophageal progenitor cells contribute to homeostasis and regeneration

Véronique Giroux(University of Pennsylvania), Ashley Lento(University of Pennsylvania), Mirazul Islam(Dana-Farber Cancer Institute), Jason R. Pitarresi(University of Pennsylvania), Akriti Kharbanda(University of Pennsylvania), Kathryn E. Hamilton(University of Pennsylvania), Kelly A. Whelan(University of Pennsylvania), Apple Long(University of Pennsylvania), Ben Rhoades(University of Pennsylvania), Qiaosi Tang(University of Pennsylvania), Hiroshi Nakagawa(University of Pennsylvania), Christopher J. Lengner(California Institute for Regenerative Medicine), Adam J. Bass(Harvard University), E. Paul Wileyto(University of Pennsylvania), Andres J. Klein–Szanto(Fox Chase Cancer Center), Timothy C. Wang(Columbia University), Anil K. Rustgi(University of Pennsylvania)
Journal of Clinical Investigation
May 7, 2017
Cited by 117Open Access
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Abstract

The esophageal lumen is lined by a stratified squamous epithelium comprised of proliferative basal cells that differentiate while migrating toward the luminal surface and eventually desquamate. Rapid epithelial renewal occurs, but the specific cell of origin that supports this high proliferative demand remains unknown. Herein, we have described a long-lived progenitor cell population in the mouse esophageal epithelium that is characterized by expression of keratin 15 (Krt15). Genetic in vivo lineage tracing revealed that the Krt15 promoter marks a long-lived basal cell population able to self-renew, proliferate, and generate differentiated cells, consistent with a progenitor/stem cell population. Transcriptional profiling demonstrated that Krt15+ basal cells are molecularly distinct from Krt15- basal cells. Depletion of Krt15-derived cells resulted in decreased proliferation, thereby leading to atrophy of the esophageal epithelium. Further, Krt15+ cells were radioresistant and contributed to esophageal epithelial regeneration following radiation-induced injury. These results establish the presence of a long-lived and indispensable Krt15+ progenitor cell population that provides additional perspective on esophageal epithelial biology and the widely prevalent diseases that afflict this epithelium.


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