Author:
Tsao Po-Nien,Matsuoka Chisa,Wei Shu-Chen,Sato Atsuyasu,Sato Susumu,Hasegawa Koichi,Chen Hung-kuan,Ling Thai-Yen,Mori Munemasa,Cardoso Wellington V.,Morimoto Mitsuru
Abstract
Abnormal enlargement of the alveolar spaces is a hallmark of conditions such as chronic obstructive pulmonary disease and bronchopulmonary dysplasia. Notch signaling is crucial for differentiation and regeneration and repair of the airway epithelium. However, how Notch influences the alveolar compartment and integrates this process with airway development remains little understood. Here we report a prominent role of Notch signaling in the epithelial–mesenchymal interactions that lead to alveolar formation in the developing lung. We found that alveolar type II cells are major sites of Notch2 activation and show by Notch2-specific epithelial deletion (Notch2cNull) a unique contribution of this receptor to alveologenesis. Epithelial Notch2 was required for type II cell induction of the PDGF-A ligand and subsequent paracrine activation of PDGF receptor-α signaling in alveolar myofibroblast progenitors. Moreover, Notch2 was crucial in maintaining the integrity of the epithelial and smooth muscle layers of the distal conducting airways. Our data suggest that epithelial Notch signaling regulates multiple aspects of postnatal development in the distal lung and may represent a potential target for intervention in pulmonary diseases.
Funder
Ministry of Education, Culture, Sports, Science, and Technology
National Health Research Institutes
Ministry of Science and Technology, Taiwan
Foundation for the National Institutes of Health
National Taiwan University
National Taiwan University Hospital
Publisher
Proceedings of the National Academy of Sciences
Cited by
95 articles.
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