The goal of this project is to investigate mechanisms responsible for the emergence and diversification of airway epithelial cells in the respiratory system. Multiciliated cells are a crucial component of the airway epithelium, being responsible for ciliary transport in concert with water and ion transport for optimization of airway clearance, in addition to being unique sites for expression of drug transporters and growth factor receptors. Altered number, morphology or function of ciliated cells is associated with a variety of diseases, including asthma, chronic obstructive pulmonary disease (COPD) and ciliopathies, such as primary ciliary dyskinesia (PCD). Our preliminary studies implicate Notch as a critical signal for ciliated versus secretory cell fate selection during development;moreover, E2F4 has been shown to be essential to form multiciliated cells in the respiratory epithelium. Recently the Hippo-YAP pathway has emerged as a major regulator of cell growth and differentiation, being also implicated in ciliogenesis. Nevertheless, how Notch, E2F4 and Hippo-YAP influence the molecular and cellular events associated with differentiation of the airway epithelium and how multiciliated cells become distinct regionally or in response to injury, is unclear. We propose to address these questions using gain and loss function genetic models and a well-established primary airway epithelial culture system. Thus, in this project we propose to: 1) Investigate the cellular and molecular events associated with initiation of ciliated cell fate in the developing airways, looking at the role of E2F4 and Notch signaling;2) Study the role of Hippo-YAP in ciliogenesis by manipulating YAP expression or phosphorylation in vivo and in primary airway epithelial cultures;3) Study mechanisms that modulate the ciliated cell phenotype in airway progenitors of the developing lung, focusing on the Notch pathway.

Public Health Relevance

In spite of the major recent advances in the field of lung biology, the mechanisms that control epithelial differentiation and establishes the proper distribution of cellular phenotypes along the airway epithelium are still little understood. The studies in this proposal focus on the understanding of how the program of ciliated cell differentiation is established in airway progenitors and how features, such as cilia length and number per cell are regulated to generate diversity of the ciliated phenotype in the respiratory tract. PHS 398/2590 (Rev. 06/09) Page Continuation Format Page

National Institute of Health (NIH)
Research Project (R01)
Project #
Application #
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Banks-Schlegel, Susan P
Project Start
Project End
Budget Start
Budget End
Support Year
Fiscal Year
Total Cost
Indirect Cost
Columbia University (N.Y.)
Internal Medicine/Medicine
Schools of Medicine
New York
United States
Zip Code
Yao, Yao; Minor, Paul J; Zhao, Ying-Tao et al. (2016) Cis-regulatory architecture of a brain signaling center predates the origin of chordates. Nat Genet 48:575-80
Szymaniak, Aleksander D; Mahoney, John E; Cardoso, Wellington V et al. (2015) Crumbs3-Mediated Polarity Directs Airway Epithelial Cell Fate through the Hippo Pathway Effector Yap. Dev Cell 34:283-96
Awata, Junya; Song, Kangkang; Lin, Jianfeng et al. (2015) DRC3 connects the N-DRC to dynein g to regulate flagellar waveform. Mol Biol Cell 26:2788-800
Mori, Munemasa; Mahoney, John E; Stupnikov, Maria R et al. (2015) Notch3-Jagged signaling controls the pool of undifferentiated airway progenitors. Development 142:258-67