Controlled human exposures to diesel exhaust: a human epigenome-wide experiment of target bronchial epithelial cells. Issue 1 (9th April 2021)

• Record Type: Journal Article
• Authors: Cardenas, Andres; Fadadu, Raj P; Van Der Laan, Lars; Ward-Caviness, Cavin; Granger, Louis; Diaz-Sanchez, David; Devlin, Robert B; Bind, Marie-Abèle
• Editors: Goodrich, Jaclyn
• Is Part Of: Environmental epigenetics. Volume 7:Issue 1(2021)
• Publication Date: 2021-04-09
• Subjects: diesel exhaust -- respiratory health -- epigenetics -- DNA methylation -- EWAS; Epigenetics -- Periodicals; 572.86505
• DOI: 10.1093/eep/dvab003
• Languages: English
• ISSNs: 2058-5888

Abstract

Abstract: Diesel exhaust (DE) is a major contributor to ambient air pollution around the world. It is a known human carcinogen that targets the respiratory system and increases risk for many diseases, but there is limited research on the effects of DE exposure on the epigenome of human bronchial epithelial cells. Understanding the epigenetic impact of this environmental pollutant can elucidate biological mechanisms involved in the pathogenesis of harmful DE-related health effects. To estimate the causal effect of short-term DE exposure on the bronchial epithelial epigenome, we conducted a controlled single-blinded randomized crossover human experiment of exposure to DE and used bronchoscopy and Illumina 450K arrays for data collection and analysis, respectively. Of the 13 participants, 11 (85%) were male and 2 (15%) were female, and 12 (92%) were White and one (8%) was Hispanic; the mean age was 26 years (SD = 3.8 years). Eighty CpGs were differentially methylated, achieving the minimum possible exact P -value of P = 2.44 × 10 −4 ( i.e. 2/2 13 ). In regional analyses, we found two differentially methylated regions (DMRs) annotated to the chromosome 5 open reading frame 63 genes ( C5orf63 ; 7-CpGs) and unc-45 myosin chaperone A gene ( UNC45A ; 5-CpGs). Both DMRs showed increased DNA methylation after DE exposure. The average causal effects for the DMRs ranged from 1.5% to 6.0% increases in DNA methylation at individual CpGs. In conclusion, we found that short-term DE alters DNA methylation of genes in target bronchial epithelial cells, demonstrating epigenetic level effects of exposure that could be implicated in pulmonary pathologies.