N. Mookherjee, M. Ryu, M. Hemshekhar, V. Spicer, C. Carlsten
{"title":"Inhaled diesel exhaust alters plasma proteome signature","authors":"N. Mookherjee, M. Ryu, M. Hemshekhar, V. Spicer, C. Carlsten","doi":"10.1183/13993003.CONGRESS-2018.PA1269","DOIUrl":null,"url":null,"abstract":"Introduction: Diesel exhaust (DE), a paradigm for traffic-related air pollution, is associated with respiratory and cardiovascular diseases. The aim of this study was to define changes in global proteins (proteome) in plasma following exposure to inhaled DE, using a controlled human exposure study. Methods: Ex-smokers (n=6) inhaled filtered air (FA) and DE (300 mg PM2.5/m3) for 2h (crossover; random order). Plasma was obtained 24h after each exposure. Plasma (n=12) were probed in Slow off-rate modified aptamer (SOMAmer®)-based proteomic array. Differential analysis with Welch’s t-test was used to identify proteins significantly altered by inhaled DE compared to FA. Abundance of selected proteins were independently quantified using ELISA or immunoblots, in plasma obtained from healthy individuals following DE and FA exposure, to further validate proteins enhanced by DE. Results: 342 plasma proteins were significantly altered by DE compared to FA (Fig. 1). The top 20 proteins enhanced by DE were enriched to GO biological process of immune response; inflammation or cardiovascular disease. Conclusion: This is the first comprehensive interrogation of the plasma proteome to identify proteins altered following inhaled DE exposure in humans, and adds functional plausibility to observations of adverse health effects therein.","PeriodicalId":12709,"journal":{"name":"Genes and Environment","volume":" ","pages":""},"PeriodicalIF":2.7000,"publicationDate":"2018-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Genes and Environment","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1183/13993003.CONGRESS-2018.PA1269","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 1
Abstract
Introduction: Diesel exhaust (DE), a paradigm for traffic-related air pollution, is associated with respiratory and cardiovascular diseases. The aim of this study was to define changes in global proteins (proteome) in plasma following exposure to inhaled DE, using a controlled human exposure study. Methods: Ex-smokers (n=6) inhaled filtered air (FA) and DE (300 mg PM2.5/m3) for 2h (crossover; random order). Plasma was obtained 24h after each exposure. Plasma (n=12) were probed in Slow off-rate modified aptamer (SOMAmer®)-based proteomic array. Differential analysis with Welch’s t-test was used to identify proteins significantly altered by inhaled DE compared to FA. Abundance of selected proteins were independently quantified using ELISA or immunoblots, in plasma obtained from healthy individuals following DE and FA exposure, to further validate proteins enhanced by DE. Results: 342 plasma proteins were significantly altered by DE compared to FA (Fig. 1). The top 20 proteins enhanced by DE were enriched to GO biological process of immune response; inflammation or cardiovascular disease. Conclusion: This is the first comprehensive interrogation of the plasma proteome to identify proteins altered following inhaled DE exposure in humans, and adds functional plausibility to observations of adverse health effects therein.
期刊介绍:
Genes and Environment is an open access, peer-reviewed journal that aims to accelerate communications among global scientists working in the field of genes and environment. The journal publishes articles across a broad range of topics including environmental mutagenesis and carcinogenesis, environmental genomics and epigenetics, molecular epidemiology, genetic toxicology and regulatory sciences.
Topics published in the journal include, but are not limited to, mutagenesis and anti-mutagenesis in bacteria; genotoxicity in mammalian somatic cells; genotoxicity in germ cells; replication and repair; DNA damage; metabolic activation and inactivation; water and air pollution; ROS, NO and photoactivation; pharmaceuticals and anticancer agents; radiation; endocrine disrupters; indirect mutagenesis; threshold; new techniques for environmental mutagenesis studies; DNA methylation (enzymatic); structure activity relationship; chemoprevention of cancer; regulatory science. Genetic toxicology including risk evaluation for human health, validation studies on testing methods and subjects of guidelines for regulation of chemicals are also within its scope.