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ABSTRACT: Introduction
Fatty acid metabolism plays a crucial role in regulating airway inflammation through the synthesis of lipid mediators. We have previously demonstrated that a 12/15-lipoxygenase (12/15-LOX or Alox15)-derived mediator attenuates IL-33-induced eosinophilic airway inflammation in mice. However, the cellular sources of these mediators remain unclear.Methods
To identify the cellular sources, we used several cell type-specific conditional 12/15-LOX-deficient mice.Results
We found that eosinophils and pleural macrophages were the major 12/15-LOX-expressing cell types responsible for attenuating airway inflammation. Eosinophils were the major population of 12/15-LOX-expressing cells found in inflamed lung tissue. In addition, pleural macrophages were the major p
SUBMITTER: Ito E
PROVIDER: S-EPMC12043891 | biostudies-literature | 2025
REPOSITORIES: biostudies-literature