Generation of multiciliated cells in functional airway epithelia from human induced pluripotent stem cells

被引:160
作者
Firth, Amy L. [1 ]
Dargitz, Carl T. [1 ]
Qualls, Susan J. [1 ]
Menon, Tushar [1 ]
Wright, Rebecca [1 ]
Singer, Oded [1 ]
Gage, Fred H. [1 ]
Khanna, Ajai [2 ]
Verma, Inder M. [1 ]
机构
[1] Salk Inst Biol Studies, Genet Lab, La Jolla, CA 92037 USA
[2] Univ Calif San Diego, Dept Surg, San Diego, CA 92013 USA
关键词
differentiation; definitive endoderm; bronchi; MOUSE LUNG DEVELOPMENT; CLARA CELLS; CYSTIC-FIBROSIS; GROWTH-FACTOR; RAT LUNG; BRANCHING MORPHOGENESIS; TRACHEAL EPITHELIUM; MUCOUS METAPLASIA; GOBLET CELLS; II CELLS;
D O I
10.1073/pnas.1403470111
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
Despite therapeutic advancement, pulmonary disease still remains a major cause of morbidity and mortality around the world. Opportunities to study human lung disease either in vivo or in vitro are currently limited. Using induced pluripotent stem cells (iPSCs), we generated mature multiciliated cells in a functional airway epithelium. Robust multiciliogenesis occurred when notch signaling was inhibited and was confirmed by (i) the assembly of multiple pericentrin-stained centrioles at the apical surface, (ii) expression of transcription factor forkhead box protein J1, and (iii) presence of multiple acetylated tubulin-labeled cilia projections in individual cells. Clara, goblet, and basal cells were all present, confirming the generation of a complete polarized epithelial-cell layer. Additionally, cAMP-activated and cystic fibrosis transmembrane regulator inhibitor 172-sensitive cystic fibrosis transmembrane regulator currents were recorded in isolated epithelial cells. Our report demonstrating the generation of mature multiciliated cells in respiratory epithelium from iPSCs is a significant advance toward modeling a number of human respiratory diseases in vitro.
引用
收藏
页码:E1723 / E1730
页数:8
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