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

被引:79
作者
Giroux, Veronique [1 ,2 ]
Lento, Ashley A. [1 ,2 ]
Islam, Mirazul [3 ]
Pitarresi, Jason R. [1 ,2 ]
Kharbanda, Akriti [1 ,2 ]
Hamilton, Kathryn E. [1 ,2 ]
Whelan, Kelly A. [1 ,2 ]
Long, Apple [1 ,2 ]
Rhoades, Ben [1 ,2 ]
Tang, Qiaosi [1 ,2 ]
Nakagawa, Hiroshi [1 ,2 ]
Lengner, Christopher J. [4 ,5 ]
Bass, Adam J. [3 ,6 ]
Wileyto, E. Paul [7 ]
Klein-Szanto, Andres J. [8 ,9 ]
Wang, Timothy C. [10 ]
Rustgi, Anil K. [1 ,2 ,11 ]
机构
[1] Univ Penn, Dept Med, Div Gastroenterol, Philadelphia, PA 19104 USA
[2] Univ Penn, Abramson Canc Ctr, Philadelphia, PA 19104 USA
[3] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[4] Univ Penn, Sch Vet Med, Dept Biomed Sci, Philadelphia, PA 19104 USA
[5] Univ Penn, Inst Regenerat Med, Philadelphia, PA 19104 USA
[6] Harvard Med Sch, Boston, MA USA
[7] Univ Penn, Dept Biostat & Epidemiol, Philadelphia, PA 19104 USA
[8] Fox Chase Canc Ctr, Dept Pathol, 7701 Burholme Ave, Philadelphia, PA 19111 USA
[9] Fox Chase Canc Ctr, Canc Biol Program, 7701 Burholme Ave, Philadelphia, PA 19111 USA
[10] Columbia Univ, Dept Med, Div Digest & Liver Dis, New York, NY USA
[11] Univ Penn, Dept Genet, Philadelphia, PA 19104 USA
关键词
EPITHELIAL STEM-CELLS; HAIR FOLLICLE BULGE; INTESTINAL STEM; FUNCTIONALLY DISTINCT; REPAIR; MOUSE; POPULATION; EXPRESSION; IDENTIFICATION; MARKERS;
D O I
10.1172/JCI88941
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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.
引用
收藏
页码:2378 / 2391
页数:14
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