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Title: Myeloid cell dynamics in bleomycin-induced pulmonary injury in mice; effects of anti-TNFα antibody.

Authors: Venosa, Alessandro; Gow, James G; Taylor, Sheryse; Golden, Thea N; Murray, Alexa; Abramova, Elena; Malaviya, Rama; Laskin, Debra L; Gow, Andrew J

Published In Toxicol Appl Pharmacol, (2021 Apr 15)

Abstract: Bleomycin is a cancer therapeutic known to cause lung injury which progresses to fibrosis. Evidence suggests that macrophages contribute to this pathological response. Tumor necrosis factor (TNF)α is a macrophage-derived pro-inflammatory cytokine implicated in lung injury. Herein, we investigated the role of TNFα in macrophage responses to bleomycin. Treatment of mice with bleomycin (3 U/kg, i.t.) caused histopathological changes in the lung within 3 d which culminated in fibrosis at 21 d. This was accompanied by an early (3-7 d) influx of CD11b+ and iNOS+ macrophages into the lung, and Arg-1+ macrophages at 21 d. At this time, epithelial cell dysfunction, defined by increases in total phospholipids and SP-B was evident. Treatment of mice with anti-TNFα antibody (7.5 mg/kg, i.v.) beginning 15-30 min after bleomycin, and every 5 d thereafter reduced the number and size of fibrotic foci and restored epithelial cell function. Flow cytometric analysis of F4/80+ alveolar macrophages (AM) isolated by bronchoalveolar lavage and interstitial macrophages (IM) by tissue digestion identified resident (CD11b-CD11c+) and immature infiltrating (CD11b+CD11c-) AM, and mature (CD11b+CD11c+) and immature (CD11b+CD11c-) IM subsets in bleomycin treated mice. Greater numbers of mature (CD11c+) infiltrating (CD11b+) AM expressing the anti-inflammatory marker, mannose receptor (CD206) were observed at 21 d when compared to 7 d post bleomycin. Mature proinflammatory (Ly6C+) IM were greater at 7 d relative to 21 d. These cells transitioned into mature anti-inflammatory/pro-fibrotic (CD206+) IM between 7 and 21 d. Anti-TNFα antibody heightened the number of CD11b+ AM in the lung without altering their activation state. Conversely, it reduced the abundance of mature proinflammatory (Ly6C+) IM in the tissue at 7 d and immature pro-fibrotic IM at 21 d. Taken together, these data suggest that TNFα inhibition has beneficial effects in bleomycin induced injury, restoring epithelial function and reducing numbers of profibrotic IM and the extent of pulmonary fibrosis.

PubMed ID: 33647319 Exiting the NIEHS site

MeSH Terms: Animals; Anti-Inflammatory Agents/pharmacology*; Bleomycin; Disease Models, Animal; Epithelial Cells/drug effects; Epithelial Cells/metabolism; Epithelial Cells/pathology; Fibrosis; Lung/drug effects*; Lung/metabolism; Lung/pathology; Macrophage Activation/drug effects*; Macrophages/drug effects*; Macrophages/metabolism; Macrophages/pathology; Male; Mice, Inbred C57BL; Phenotype; Phospholipids/metabolism; Pneumonia/chemically induced; Pneumonia/metabolism; Pneumonia/pathology; Pneumonia/prevention & control*; Pulmonary Fibrosis/chemically induced; Pulmonary Fibrosis/metabolism; Pulmonary Fibrosis/pathology; Pulmonary Fibrosis/prevention & control*; Pulmonary Surfactant-Associated Proteins/metabolism; Tumor Necrosis Factor Inhibitors/pharmacology*; Tumor Necrosis Factor-alpha/antagonists & inhibitors*; Tumor Necrosis Factor-alpha/metabolism

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