Long-term polarization of alveolar macrophages to a profibrotic phenotype after inhalation exposure to multi-wall carbon nanotubes.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 30372450.
- Also identified by DOI 10.1371/journal.pone.0205702 and PMC identifier 6205598.
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Abstract
Nanomaterials are widely used in various fields. Although the toxicity of carbon nanotubes (CNTs) in pulmonary tissues has been demonstrated, the toxicological effect of CNTs on the immune system in the lung remains unclear. In this study, exposure to Taquann-treated multi-walled CNTs (T-CNTs) was performed using aerosols generated in an inhalation chamber. At 12 months after T-CNT exposure, alveolar inflammation with macrophage accumulation and hypertrophy of the alveolar walls were observed. In addition, fibrotic lesions were enhanced by T-CNT exposure. The macrophages in the bronchoalveolar lavage fluid of T-CNT-exposed mice were not largely shifted to any particular population, and were a mixed phenotype with M1 and M2 polarization. Moreover, the alveolar macrophages of T-CNT-exposed mice produced matrix metalloprotinase-12. These results suggest that T-CNT exposure promoted chronic inflammation and fibrotic lesion formation in profibrotic macrophages for prolonged periods.
Medical subject headings
- Air Pollutants
- Air Pollutants/toxicity
- Air Pollution
- Air Pollution/adverse effects
- Animals
- Bronchoalveolar Lavage Fluid
- Bronchoalveolar Lavage Fluid/cytology
- Disease Models, Animal
- Female
- Fibrosis
- Humans
- Inhalation Exposure
- Inhalation Exposure/adverse effects
- Macrophages, Alveolar
- Macrophages, Alveolar/drug effects
- Macrophages, Alveolar/immunology
- Macrophages, Alveolar/pathology
- Matrix Metalloproteinase 12
- Matrix Metalloproteinase 12/immunology
- Matrix Metalloproteinase 12/metabolism
- Mice
- Mice, Inbred C57BL
- Nanotubes, Carbon
- Nanotubes, Carbon/toxicity
- Pneumonia
- Pneumonia/chemically induced
- Pneumonia/immunology
- Pneumonia/pathology
- Pulmonary Alveoli
- Pulmonary Alveoli/cytology
- Pulmonary Alveoli/drug effects
- Pulmonary Alveoli/immunology
- Pulmonary Alveoli/pathology