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FGF10 and Human Lung Disease Across the Life Spectrum
1Department of Pediatrics, University of California, San Diego, Rady Children's Hospital, San Diego, CA, United States.
Insights
Fibroblast growth factor 10 (FGF10) is crucial for lung development and repair. Understanding FGF10
Area of Science:
- Pulmonology and Developmental Biology
- Cellular and Molecular Medicine
Background:
- Lung diseases affect all age groups, from neonates to the elderly.
- Congenital lung structure abnormalities and environmental exposures contribute to lung disease.
- Fibroblast growth factor 10 (FGF10) plays a vital role in lung development and repair.
Purpose of the Study:
- To review the cellular and molecular mechanisms linking FGF10 to various lung diseases.
- To explore FGF10's role in lung morphogenesis, differentiation, and injury response.
Main Methods:
- Literature review of studies on FGF10 signaling in lung development and disease.
- Analysis of cellular and molecular pathways involving FGF10 in lung tissue.
Main Results:
- FGF10 signaling defects during development cause neonatal lung disease, such as bronchopulmonary dysplasia.
- FGF10 mutations are linked to congenital airway abnormalities and increased risk of adult chronic lung diseases, including cystic fibrosis.
- FGF10 is essential for maintaining airway progenitor cells and promoting alveolar regeneration after injury.
Conclusions:
- FGF10 is a key regulator in multiple lung diseases across the lifespan.
- Targeting FGF10 pathways may offer novel therapeutic strategies for diverse lung conditions.
Abstract:
Lung diseases impact patients across the lifespan, from infants in the first minutes of life through the aged population. Congenital abnormalities of lung structure can cause lung disease at birth or make adults more susceptible to chronic disease. Continuous inhalation of atmospheric components also requires the lung to be resilient to cellular injury. Fibroblast growth factor 10 (FGF10) regulates multiple stages of structural lung morphogenesis, cellular differentiation, and the response to injury. As a driver of lung airway branching morphogenesis, FGF10 signaling defects during development lead to neonatal lung disease. Alternatively, congenital airway abnormalities attributed to FGF10 mutations increase the risk of chronic airway disease in adulthood. FGF10 also maintains progenitor cell populations in the airway and promotes alveolar type 2 cell expansion and differentiation following injury. Here we review the cellular and molecular mechanisms linking FGF10 to multiple lung diseases, from bronchopulmonary dysplasia in extremely preterm neonates, cystic fibrosis in children, and chronic adult lung disorders. Understanding the connections between FGF10 and lung diseases may lead to exciting new therapeutic strategies.
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