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DOI 10.1073/pnas.1403470111

Медицинская библиотека · Proceedings of the National Academy of Sciences of the United States of America · 2014

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

Firth Amy L, Dargitz Carl T, Qualls Susan J, Menon Tushar, Wright Rebecca, Singer Oded, Gage Fred H, Khanna Ajai, Verma Inder M

СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

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.

Для цитирования: Firth Amy L, Dargitz Carl T, Qualls Susan J, Menon Tushar, Wright Rebecca, Singer Oded, Gage Fred H, Khanna Ajai, Verma Inder M. Generation of multiciliated cells in functional airway epithelia from human induced pluripotent stem cells.. Proceedings of the National Academy of Sciences of the United States of America. 2014. DOI: 10.1073/pnas.1403470111.

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