Therapeutic Targeting of the IL-6 Trans-Signaling/Mechanistic Target of Rapamycin Complex 1 Axis in Pulmonary Emphysema

• Published in: American journal of respiratory and critical care medicine Vol. 194; no. 12; pp. 1494 - 1505
• Main Authors: Ruwanpura, Saleela M, McLeod, Louise, Dousha, Lovisa F, Seow, Huei J, Alhayyani, Sultan, Tate, Michelle D, Deswaerte, Virginie, Brooks, Gavin D, Bozinovski, Steven, MacDonald, Martin, Garbers, Christoph, King, Paul T, Bardin, Philip G, Vlahos, Ross, Rose-John, Stefan, Anderson, Gary P, Jenkins, Brendan J
• Format: Journal Article
• Language: English
• Published: United States American Thoracic Society 15.12.2016
• Subjects: Animals; Disease Models, Animal; Humans; Interleukin-6 - immunology; Mechanistic Target of Rapamycin Complex 1; Mice; Multiprotein Complexes - pharmacology; Pulmonary Emphysema - drug therapy; Pulmonary Emphysema - immunology; Signal Transduction - drug effects; Signal Transduction - immunology; TOR Serine-Threonine Kinases - pharmacology; mouse models; mechanistic target of rapamycin complex 1; trans-signaling; pulmonary emphysema; interleukin-6
• ISSN: 1073-449X; 1535-4970
• DOI: 10.1164/rccm.201512-2368oc

The potent immunomodulatory cytokine IL-6 is consistently up-regulated in human lungs with emphysema and in mouse emphysema models; however, the mechanisms by which IL-6 promotes emphysema remain obscure. IL-6 signals using two distinct modes: classical signaling via its membrane-bound IL-6 receptor (IL-6R), and trans-signaling via a naturally occurring soluble IL-6R. To identify whether IL-6 trans-signaling and/or classical signaling contribute to the pathogenesis of emphysema. We used the gp130 genetic mouse model for spontaneous emphysema and cigarette smoke-induced emphysema models. Emphysema in mice was quantified by various methods including in vivo lung function and stereology, and terminal deoxynucleotidyl transferase dUTP nick end labeling assay was used to assess alveolar cell apoptosis. In mouse and human lung tissues, the expression level and location of IL-6 signaling-related genes and proteins were measured, and the levels of IL-6 and related proteins in sera from emphysematous mice and patients were also assessed. Lung tissues from patients with emphysema, and from spontaneous and cigarette smoke-induced emphysema mouse models, were characterized by excessive production of soluble IL-6R. Genetic blockade of IL-6 trans-signaling in emphysema mouse models and therapy with the IL-6 trans-signaling antagonist sgp130Fc ameliorated emphysema by suppressing augmented alveolar type II cell apoptosis. Furthermore, IL-6 trans-signaling-driven emphysematous changes in the lung correlated with mechanistic target of rapamycin complex 1 hyperactivation, and treatment of emphysema mouse models with the mechanistic target of rapamycin complex 1 inhibitor rapamycin attenuated emphysematous changes. Collectively, our data reveal that specific targeting of IL-6 trans-signaling may represent a novel treatment strategy for emphysema.