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Manganese dioxide induces alveolar macrophage chemotaxis for neutrophils in vitro
Abstract:
Workers exposed to airborne manganese dioxide (MnO2) may develop pneumonia resistant to chemotherapy. Previous animal experiments have demonstrated that exposure to airborne MnO2 induces an invasion of neutrophils into the airways 4-12 h after exposure. Experiments were undertaken to further study the role of alveolar macrophage (AM) in the development of this response. Guinea pig lung lavage fluid was centrifuged and washed, and cell suspension incubated on one side of a leukocyte migration chamber. MnO2 (2.5 mg/ml) was incubated with the cells for different time periods. Peritoneal neutrophils from guinea pigs were isolated and incubated on the other side of the chamber. Observations of the free lung cells demonstrated that phagocytosis of the MnO2 particles commenced immediately and was virtually completed within 30 min. Cells from control animals caused small directional migration across the filter. Cells which had phagocytosed MnO2 particles showed a significantly higher degree of neutrophil migration. The data suggest that pneumonia, in terms of neutrophil invasion into the lungs after MnO2 exposure, is associated with an activation of AM with subsequent release of neutrophil recruiting factor.
Insights
Exposure to manganese dioxide (MnO2) triggers alveolar macrophages (AM) to recruit neutrophils, potentially causing chemotherapy-resistant pneumonia. This study clarifies the role of AM in MnO2-induced lung inflammation.
Area of Science:
- Environmental Health
- Pulmonary Medicine
- Immunology
Background:
- Airborne manganese dioxide (MnO2) exposure is linked to chemotherapy-resistant pneumonia.
- Previous studies show MnO2 induces neutrophil invasion into airways within 4-12 hours.
Purpose of the Study:
- To investigate the role of alveolar macrophages (AM) in MnO2-induced lung inflammation.
- To understand the mechanism of neutrophil recruitment following MnO2 exposure.
Main Methods:
- Guinea pig alveolar macrophages were isolated and incubated with MnO2 particles.
- Leukocyte migration chambers were used to assess neutrophil migration.
- Phagocytosis of MnO2 by AM and subsequent neutrophil migration were quantified.
Main Results:
- Alveolar macrophages rapidly phagocytosed MnO2 particles within 30 minutes.
- AM that phagocytosed MnO2 showed significantly increased neutrophil migration.
- Control AM induced minimal neutrophil migration.
Conclusions:
- Alveolar macrophage activation by MnO2 is a key step in neutrophil recruitment to the lungs.
- This AM activation and subsequent release of neutrophil-recruiting factors contribute to MnO2-induced pneumonia.