Pulmonary toxicity and global gene expression changes in response to sub-chronic inhalation exposure to crystalline silica in rats

• Published in: Journal of Toxicology and Environmental Health, Part A Part A, 2017-01, Vol.80 (23-24), p.1349-1368
• Main Authors: Umbright, Christina, Sellamuthu, Rajendran, Roberts, Jenny R., Young, Shih-Houng, Richardson, Diana, Schwegler-Berry, Diane, McKinney, Walter, Chen, Bean, Gu, Ja Kook, Kashon, Michael, Joseph, Pius
• Format: Article
• Language: English
• Subjects: Alveolar Epithelial Cells - pathology; Alveoli; Animals; Bioinformatics; Bronchoalveolar Lavage Fluid - chemistry; Bronchus; Cancer; Crystal structure; Crystalline silica; Crystallinity; DNA microarrays; Exposure; Fibrosis; Fibrosis - physiopathology; Gene expression; Gene Expression Regulation; Genes; Health risks; Hyperplasia; Hyperplasia - physiopathology; Inflammation - physiopathology; Inhalation; inhalation exposure; Inhalation Exposure - adverse effects; L-Lactate dehydrogenase; Lactate dehydrogenase; Lactic acid; Leukocytes (neutrophilic); Lung - drug effects; Lungs; Macrophages; Male; mechanisms; Microarray Analysis; Molecular modelling; Oxidative stress; pulmonary toxicity; Rats; Rats, Inbred F344; Respiration; Rodents; Silica; Silicon dioxide; Silicon Dioxide - toxicity; Silicosis; Toxicity
• ISSN: 1528-7394; 1087-2620; 2381-3504
• DOI: 10.1080/15287394.2017.1384773

Exposure to crystalline silica results in serious adverse health effects, most notably, silicosis. An understanding of the mechanism(s) underlying silica-induced pulmonary toxicity is critical for the intervention and/or prevention of its adverse health effects. Rats were exposed by inhalation to crystalline silica at a concentration of 15 mg/m 3 , 6 hr/day, 5 days/week for 3, 6 or 12 weeks. Pulmonary toxicity and global gene expression profiles were determined in lungs at the end of each exposure period. Crystalline silica was visible in lungs of rats especially in the 12-week group. Pulmonary toxicity, as evidenced by an increase in lactate dehydrogenase (LDH) activity and albumin content and accumulation of macrophages and neutrophils in the bronchoalveolar lavage (BAL), was seen in animals depending upon silica exposure duration. The most severe histological changes, noted in the 12-week exposure group, consisted of chronic active inflammation, type II pneumocyte hyperplasia, and fibrosis. Microarray analysis of lung gene expression profiles detected significant differential expression of 38, 77, and 99 genes in rats exposed to silica for 3-, 6-, or 12-weeks, respectively, compared to time-matched controls. Among the significantly differentially expressed genes (SDEG), 32 genes were common in all exposure groups. Bioinformatics analysis of the SDEG identified enrichment of functions, networks and canonical pathways related to inflammation, cancer, oxidative stress, fibrosis, and tissue remodeling in response to silica exposure. Collectively, these results provided insights into the molecular mechanisms underlying pulmonary toxicity following sub-chronic inhalation exposure to crystalline silica in rats.