Basal cells as stem cells of the mouse trachea and human airway epithelium

被引:1114
作者
Rock, Jason R. [1 ]
Onaitis, Mark W. [2 ]
Rawlins, Emma L. [1 ]
Lu, Yun [1 ]
Clark, Cheryl P. [1 ]
Xue, Yan [1 ]
Randell, Scott H. [3 ]
Hogan, Brigid L. M. [1 ]
机构
[1] Duke Univ, Dept Cell Biol, Med Ctr, Durham, NC 27710 USA
[2] Duke Univ, Dept Surg, Med Ctr, Durham, NC 27710 USA
[3] Univ N Carolina, Cyst Fibrosis Pulm Res & Treatment Ctr, Chapel Hill, NC 27559 USA
基金
美国国家卫生研究院;
关键词
epithelial basal cells; lung; NGFR; stem/progenitor; sphere-forming assay; TRACHEOBRONCHIAL EPITHELIUM; CLARA CELLS; LUNG; EXPRESSION; GROWTH; DIFFERENTIATION; PROLIFERATION; MULTIPOTENT; CARCINOMAS; ESOPHAGEAL;
D O I
10.1073/pnas.0906850106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The pseudostratified epithelium of the mouse trachea and human airways contains a population of basal cells expressing Trp-63 (p63) and cytokeratins 5 (Krt5) and Krt14. Using a KRT5-CreER(T2) transgenic mouse line for lineage tracing, we show that basal cells generate differentiated cells during postnatal growth and in the adult during both steady state and epithelial repair. We have fractionated mouse basal cells by FACS and identified 627 genes preferentially expressed in a basal subpopulation vs. non-BCs. Analysis reveals potential mechanisms regulating basal cells and allows comparison with other epithelial stem cells. To study basal cell behaviors, we describe a simple in vitro clonal sphere-forming assay in which mouse basal cells self-renew and generate luminal cells, including differentiated ciliated cells, in the absence of stroma. The transcriptional profile identified 2 cell-surface markers, ITGA6 and NGFR, which can be used in combination to purify human lung basal cells by FACS. Like those from the mouse trachea, human airway basal cells both self-renew and generate luminal daughters in the sphere-forming assay.
引用
收藏
页码:12771 / 12775
页数:5
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