Evidence of an epithelial stem/progenitor cell hierarchy in the adult mouse lung

被引:278
作者
McQualter, Jonathan L. [1 ,2 ]
Yuen, Karen
Williams, Brenda
Bertoncello, Ivan [2 ]
机构
[1] Monash Univ, Australian Stem Cell Ctr, Clayton, Vic 3800, Australia
[2] Monash Univ, Dept Anat & Dev Biol, Clayton, Vic 3800, Australia
基金
英国医学研究理事会;
关键词
colony-forming assay; lung epithelium; lineage specificity; differentiation; EpCAM; STEM-CELLS; PROGENITOR CELLS; ALVEOLAR; GROWTH; DIFFERENTIATION; MORPHOGENESIS; ALVEOGENESIS; TRACHEA; REPAIR; AIRWAY;
D O I
10.1073/pnas.0909207107
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 role of lung epithelial stem cells in maintenance and repair of the adult lung is ill-defined, and their identity remains contentious because of the lack of definitive markers for their prospective isolation and the absence of clonogenic assays able to measure their stem/progenitor cell potential. In this study, we show that replication of epithelial-mesenchymal interactions in a previously undescribed matrigel-based clonogenic assay enables the identification of lung epithelial stem/progenitor cells by their colony-forming potential in vitro. We describe a population of EpCAM(hi) CD49f(pos) CD104(pos) CD24(low) epithelial cfus that generate colonies comprising airway, alveolar, or mixed lung epithelial cell lineages when cocultured with EpCAM(neg) Sca-1(pos) lung mesenchymal cells. We show that soluble fibroblast growth factor-10 and hepatocyte growth factor partially replace the requirement for mesenchymal support of epithelial colony formation, allowing clonal passaging and demonstration of their capacity for self-renewal. These data support a model in which the adult mouse lung contains a minor population of multipotent epithelial stem/progenitor cells with the capacity for self-renewal and whose descendants give rise to airway and alveolar epithelial cell lineages in vitro.
引用
收藏
页码:1414 / 1419
页数:6
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