Structural Lung Remodeling Precedes Functional Decline After Chronic Smoldering Douglas Fir Smoke Exposure in Apoe-/- Mice
Charbel Yazbeck, Jacqueline MatziD, Matthew EdeniD, Shubham Rajput, Ye CheniD, Michael J. GollneriD, Paola Sebastiani BiD, Chiara Maria BelliniiD, Jessica M. OakesiD
Abstract
Wildland firefighters experience repeated exposure to wildfire smoke, yet the pathophysiological mechanisms underlying chronic inhalation injury remain poorly understood. Although prior studies report parenchymal destruction following prolonged woodsmoke exposure, the temporal relationship between molecular, structural, and functional decline following inhalation of smoke from needles/leaves remains unclear. To address this gap, we characterized coordinated changes in lung structure, function, and underlying molecular disruptions using a dosimetry-based murine model approximating 7-14 years of firefighter service. Male apolipoprotein E-deficient mice were exposed to smoldering Douglas fir needle smoke (40 mg/m3, 2 h/day, 5 days/week) for 8 or 16 weeks. Immunofluorescence analyses revealed an early elastolytic response at 8 weeks, with increased neutrophil elastases and matrix metalloproteinases-9 and -12, accompanied by elevated surfactant protein-D, compared to air controls. These changes were resolved by 16 weeks despite progressive tissue injury. Airspace enlargement was evident at 8 weeks, progressed by 16 weeks, and included increased alveolar blunting and septal wall thickening at the later time point. Cleaved caspase-3 was elevated at 16 weeks, indicative of advanced parenchymal damage and apoptosis. Epithelial tight-junction protein ZO-1 intensity was reduced at both evaluation points, whereas the epithelial-to-mesenchymal marker N-cadherin remained undetectable in the alveolar epithelium. Functional impairment as evident by increased static compliance and upward shifts in pressure-volume curves was only significant after 16 weeks of exposure. Findings indicate that molecular and structural injury of tissue destruction preceded measurable functional decline, underscoring the need for early biomarkers to identify smoke-induced lung injury in wildland firefighters before function loss occurs.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 0
- Organism
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Occupationally Relevant Wildfire Smoke Inhalation Impairs Nitric Oxide Signaling and Promotes Progressive Aortic Stiffening in Hypercholesterolemic Mice
Jacqueline Matz, Victoria A. Williams, … Chiara Maria Bellini·bioRxiv·May 20, 2026
- Lymphatic Thrombosis and Impaired Lymph Drainage in Cigarette Smoke-Associated Emphysema
B. D. Summers, K. Kim, … H. O. Reed·bioRxiv·Nov 23, 2021
- Persistent transcriptomic changes following repeated exposure to wood smoke in non-human primate airway epithelial cells
Evan Holmes, Anthony P. C. Brown, … Hong Ji·Current ZoologyPeer-reviewed·Jan 1, 2026
- The memory of airway epithelium damage in smokers and COPD patients
F. M. Carlier, B. Detry, … C. Pilette·bioRxiv·Apr 21, 2021
- The effect of enriched versus inadequate housing conditions on eucalyptus smoke-induced cardiovascular dysfunction in mice
Molly E. Harmon, Michelle E. Fiamingo, … Mehdi Saeed Hazari·Inhalation ToxicologyPeer-reviewed·May 22, 2024
- Eosinophils restrict diesel exhaust particles induced cell proliferation of lung epithelial A549 cells, vial interleukin-13 mediated mechanisms: implications for tissue remodelling and fibrosis
R. Niranjan, M. Subramanian, … S. K. Ojha·bioRxiv·Mar 30, 2021