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Usage Information

IGF1R controls mechanosignaling in myofibroblasts required for pulmonary alveologenesis
Hua He, John Snowball, Fei Sun, Cheng-Lun Na, Jeffrey A. Whitsett
Hua He, John Snowball, Fei Sun, Cheng-Lun Na, Jeffrey A. Whitsett
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Research Article Pulmonology

IGF1R controls mechanosignaling in myofibroblasts required for pulmonary alveologenesis

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Abstract

Ventilation throughout life is dependent on the formation of pulmonary alveoli, which create an extensive surface area in which the close apposition of respiratory epithelium and endothelial cells of the pulmonary microvascular enables efficient gas exchange. Morphogenesis of the alveoli initiates at late gestation in humans and the early postnatal period in the mouse. Alveolar septation is directed by complex signaling interactions among multiple cell types. Here, we demonstrate that IGF1 receptor gene (Igf1r) expression by a subset of pulmonary fibroblasts is required for normal alveologenesis in mice. Postnatal deletion of Igf1r caused alveolar simplification, disrupting alveolar elastin networks and extracellular matrix without altering myofibroblast differentiation or proliferation. Moreover, loss of Igf1r impaired contractile properties of lung myofibroblasts and inhibited myosin light chain (MLC) phosphorylation and mechanotransductive nuclear YAP activity. Activation of p-AKT, p-MLC, and nuclear YAP in myofibroblasts was dependent on Igf1r. Pharmacologic activation of AKT enhanced MLC phosphorylation, increased YAP activation, and ameliorated alveolar simplification in vivo. IGF1R controls mechanosignaling in myofibroblasts required for lung alveologenesis.

Authors

Hua He, John Snowball, Fei Sun, Cheng-Lun Na, Jeffrey A. Whitsett

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Usage data is cumulative from December 2024 through December 2025.

Usage JCI PMC
Text version 525 157
PDF 128 23
Figure 355 2
Supplemental data 55 1
Citation downloads 109 0
Totals 1,172 183
Total Views 1,355
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