Neutrophil-Derived IL-6 Limits Alveolar Barrier Disruption in Experimental Ventilator-Induced Lung Injury

• Published in: The Journal of immunology (1950) 2009-06, Vol.182 (12), p.8056-8062
• Main Authors: Wolters, Paul J, Wray, Charlie, Sutherland, Rachel E, Kim, Sophia S, Koff, Jon, Mao, Ying, Frank, James A
• Format: Article
• Language: English
• Subjects: Alveolar Process - immunology; Animals; Cell Adhesion; Cell Movement; Cells, Cultured; Interleukin-6 - deficiency; Interleukin-6 - genetics; Interleukin-6 - immunology; Interleukin-6 - metabolism; Leukocyte Count; Mice; Mice, Knockout; Neutrophils - cytology; Neutrophils - immunology; Neutrophils - metabolism; Peroxidase - metabolism; Rats; Ventilator-Induced Lung Injury - genetics; Ventilator-Induced Lung Injury - immunology; Ventilator-Induced Lung Injury - metabolism; Ventilator-Induced Lung Injury - pathology
• ISSN: 0022-1767; 1550-6606
• DOI: 10.4049/jimmunol.0801323

IL-6 is a biological marker of ventilator-associated lung injury that may contribute to alveolar barrier dysfunction in acute respiratory distress syndrome. To determine whether IL-6 affects alveolar barrier disruption in a model of ventilator-induced lung injury, we examined alveolar barrier albumin flux in wild-type (WT) mice given an IL-6-blocking Ab (IL6AB) and mice deficient in IL-6 (IL6KO). Albumin flux was significantly higher in mice given IL6AB compared with mice given a control Ab. Unexpectedly, albumin flux was similar in WT and IL6KO mice. To examine the mechanisms for these findings, lung neutrophil accumulation (myeloperoxidase activity) was compared, revealing a correlation between lung neutrophil accumulation and albumin flux. IL6AB mice had significantly more lung neutrophils than WT and IL6KO mice, which were similar. Therefore, to determine whether the cellular source of IL-6 influences neutrophil accumulation and alveolar barrier function, chimeric mice were compared. WT/KO chimeras (WT mice with IL6KO hematopoietic cells) showed significantly greater albumin flux and neutrophil accumulation with mechanical ventilation than WT/WT mice. Neutrophil depletion decreased albumin flux in WT and WT/KO mice. IL6KO neutrophils were more adherent in an in vitro assay compared with WT neutrophils. IL-6 from a hematopoietic cell source limits alveolar barrier disruption potentially by reducing neutrophil contact with the endothelium. Modulation of IL-6 signaling in a cell type-specific fashion may be a therapeutic target for patients with acute lung injury.