Silicosis and Silica-Induced Autoimmunity in the Diversity Outbred Mouse

• Published in: Frontiers in immunology Vol. 9; p. 874
• Main Authors: Mayeux, Jessica M, Escalante, Gabriela M, Christy, Joseph M, Pawar, Rahul D, Kono, Dwight H, Pollard, Kenneth M
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media S.A 26.04.2018
• Subjects: Animals; Antibodies, Antinuclear - immunology; autoantibody; Autoimmunity; Bronchoalveolar Lavage Fluid - immunology; Collaborative Cross Mice; Disease Models, Animal; diversity outbred; Female; Glomerulonephritis - blood; Glomerulonephritis - immunology; Glomerulonephritis - pathology; Humans; Immunology; inflammation; Kidney - immunology; Kidney - pathology; Lung - immunology; Lung - pathology; Male; Mice; Sex Factors; silica; Silicon Dioxide - immunology; silicosis; Silicosis - blood; Silicosis - immunology; Silicosis - pathology; diversity outbred; environmental autoimmunity; lung; silicosis; autoantibody; autoimmunity; inflammation; silica
• ISSN: 1664-3224; 1664-3224
• DOI: 10.3389/fimmu.2018.00874

Epidemiological studies have confidently linked occupational crystalline silica exposure to autoimmunity, but pathogenic mechanisms and role of genetic predisposition remain poorly defined. Although studies of single inbred strains have yielded insights, understanding the relationships between lung pathology, silica-induced autoimmunity, and genetic predisposition will require examination of a broad spectrum of responses and susceptibilities. We defined the characteristics of silicosis and autoimmunity and their relationships using the genetically heterogeneous diversity outbred (DO) mouse population and determined the suitability of this model for investigating silica-induced autoimmunity. Clinically relevant lung and autoimmune phenotypes were assessed 12 weeks after a transoral dose of 0, 5, or 10 mg crystalline silica in large cohorts of DO mice. Data were further analyzed for correlations, hierarchical clustering, and sex effects. DO mice exhibited a wide range of responses to silica, including mild to severe silicosis and importantly silica-induced systemic autoimmunity. Strikingly, about half of PBS controls were anti-nuclear antibodies (ANA) positive, however, few had disease-associated specificities, whereas most ANAs in silica-exposed mice showed anti-ENA5 reactivity. Correlation and hierarchical clustering showed close association of silicosis, lung biomarkers, and anti-ENA5, while other autoimmune characteristics, such as ANA and glomerulonephritis, clustered separately. Silica-exposed males had more lung inflammation, bronchoalveolar lavage fluid cells, IL-6, and autoantibodies. DO mice are susceptible to both silicosis and silica-induced autoimmunity and show substantial individual variations reflecting their genetic diverseness and the importance of predisposition particularly for autoimmunity. This model provides a new tool for deciphering the relationship between silica exposure, genes, and disease.