| Literature DB >> 32394892 |
Kuan Zhang1, Erica Yao1, Chuwen Lin1, Yu-Ting Chou1, Julia Wong1, Jianying Li1, Paul J Wolters1, Pao-Tien Chuang1.
Abstract
Alveolar formation increases the surface area for gas-exchange and is key to the physiological function of the lung. Alveolar epithelial cells, myofibroblasts and endothelial cells undergo coordinated morphogenesis to generate epithelial folds (secondary septa) to form alveoli. A mechanistic understanding of alveologenesis remains incomplete. We found that the planar cell polarity (PCP) pathway is required in alveolar epithelial cells and myofibroblasts for alveologenesis in mammals. Our studies uncovered a Wnt5a-Ror2-Vangl2 cascade that endows cellular properties and novel mechanisms of alveologenesis. This includes PDGF secretion from alveolar type I and type II cells, cell shape changes of type I cells and migration of myofibroblasts. All these cellular properties are conferred by changes in the cytoskeleton and represent a new facet of PCP function. These results extend our current model of PCP signaling from polarizing a field of epithelial cells to conferring new properties at subcellular levels to regulate collective cell behavior.Entities:
Keywords: alveolar epithelial cell; alveolus; cytoskeleton; developmental biology; lung; mouse; myofibroblast; planar cell polarity
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Year: 2020 PMID: 32394892 PMCID: PMC7217702 DOI: 10.7554/eLife.53688
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140