Characterization of Lung Fibroblasts More than Two Decades after Mustard Gas Exposure

• Published in: PloS one 2015-12, Vol.10 (12), p.e0145148-e0145148
• Main Authors: Pirzad Jahromi, Gila, Ghanei, Mostafa, Hosseini, Seyed Kazem, Shamsaei, Alireza, Gholipourmalekabadi, Mazaher, Koochaki, Ameneh, Karkuki Osguei, Nushin, Samadikuchaksaraei, Ali
• Format: Article
• Language: English
• Subjects: Actin; Airway management; Apoptosis; Biopsy; Bronchopneumonia; Case-Control Studies; Cells, Cultured; Chemical Warfare Agents - toxicity; Complications; Exposure; Female; Fibroblasts; Fibroblasts - drug effects; Fibroblasts - ultrastructure; Filopodia; Gene expression; Genetic aspects; Humans; Lung - drug effects; Lung - pathology; Lungs; Male; Medicine; Middle Aged; Molecular biology; Muscles; Mustard (Condiment); Mustard gas; Mustard Gas - toxicity; Obliterative bronchiolitis; Pathology; Patients; Penicillin; Pulmonary fibrosis; Reaction Time; Respiratory system; Rodents; Smooth muscle; Studies; Sulfur; Transplants & implants; Viability
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0145148

In patients with short-term exposure to the sulfur mustard gas, the delayed cellular effects on lungs have not been well understood yet. The lung pathology shows a dominant feature consistent with obliterative bronchiolitis, in which fibroblasts play a central role. This study aims to characterize alterations to lung fibroblasts, at the cellular level, in patients with delayed respiratory complications after short-term exposure to the sulfur mustard gas. Fibroblasts were isolated from the transbronchial biopsies of patients with documented history of exposure to single high-dose sulfur mustard during 1985-7 and compared with the fibroblasts of control subjects. Compared with controls, patients' fibroblasts were thinner and shorter, and showed a higher population doubling level, migration capacity and number of filopodia. Sulfur mustard decreased the in vitro viability of fibroblasts and increased their sensitivity to induction of apoptosis, but did not change the rate of spontaneous apoptosis. In addition, higher expression of alpha smooth muscle actin showed that the lung's microenvironment in these patients is permissive for myofibroblastic differentiation. These findings suggest that in patients under the study, the delayed pulmonary complications of sulfur mustard should be considered as a unique pathology, which might need a specific management by manipulation of cellular components.