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Publication : Cell competition drives bronchiolization and pulmonary fibrosis.

First Author  Warren R Year  2024
Journal  Nat Commun Volume  15
Issue  1 Pages  10624
PubMed ID  39639058 Mgi Jnum  J:360649
Mgi Id  MGI:7787668 Doi  10.1038/s41467-024-54997-2
Citation  Warren R, et al. (2024) Cell competition drives bronchiolization and pulmonary fibrosis. Nat Commun 15(1):10624
abstractText  Idiopathic pulmonary fibrosis (IPF) is a progressive respiratory scarring disease arising from the maladaptive differentiation of lung stem cells into bronchial epithelial cells rather than into alveolar type 1 (AT1) cells, which are responsible for gas exchange. Here, we report that healthy lungs maintain their stem cells through tonic Hippo and beta-catenin signaling, which promote Yap/Taz degradation and allow for low-level expression of the Wnt target gene Myc. Inactivation of upstream activators of the Hippo pathway in lung stem cells inhibits this tonic beta-catenin signaling and Myc expression and promotes their Taz-mediated differentiation into AT1 cells. Vice versa, increased Myc in collaboration with Yap promotes the differentiation of lung stem cells along the basal and myoepithelial-like lineages allowing them to invade and bronchiolize the lung parenchyma in a process reminiscent of submucosal gland development. Our findings indicate that stem cells exhibiting the highest Myc levels become supercompetitors that drive remodeling, whereas loser cells with lower Myc levels terminally differentiate into AT1 cells.
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