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      Extracellular vesicle-packaged miRNA release after short-term exposure to particulate matter is associated with increased coagulation

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          Abstract

          Background

          Exposure to particulate matter (PM) is associated with increased incidence of cardiovascular disease and increased coagulation, but the molecular mechanisms underlying these associations remain unknown. Obesity may increase susceptibility to the adverse effects of PM exposure, exacerbating the effects on cardiovascular diseases. Extracellular vesicles (EVs), which travel in body fluids and transfer microRNAs (miRNAs) between tissues, might play an important role in PM-induced cardiovascular risk. We sought to determine whether the levels of PM with an aerodynamic diameter ≤ 10 μm (PM 10) are associated with changes in fibrinogen levels, EV release, and the miRNA content of EVs (EV-miRNAs), investigating 1630 overweight/obese subjects from the SPHERE Study.

          Results

          Short-term exposure to PM 10 (Day before blood drawing) was associated with an increased release of EVs quantified by nanoparticle tracking analysis, especially EVs derived from monocyte/macrophage components (CD14+) and platelets (CD61+) which were characterized by flow cytometry. We first profiled miRNAs of 883 subjects by the QuantStudio™ 12 K Flex Real Time PCR System and the top 40 EV-miRNAs were validated through custom miRNA plates. Nine EV-miRNAs (let-7c-5p; miR-106a-5p; miR-143-3p; miR-185-5p; miR-218-5p; miR-331-3p; miR-642-5p; miR-652-3p; miR-99b-5p) were downregulated in response to PM 10 exposure and exhibited putative roles in cardiovascular disease, as highlighted by integrated network analysis. PM 10 exposure was significantly associated with elevated fibrinogen levels, and five of the nine downregulated EV-miRNAs were mediators between PM 10 exposure and fibrinogen levels.

          Conclusions

          Research on EVs opens a new path to the investigation of the adverse health effects of air pollution exposure. EVs have the potential to act both as markers of PM susceptibility and as potential molecular mechanism in the chain of events connecting PM exposure to increased coagulation, which is frequently linked to exposure and CVD development.

          Electronic supplementary material

          The online version of this article (doi:10.1186/s12989-017-0214-4) contains supplementary material, which is available to authorized users.

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          Most cited references26

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          A comparative risk assessment of burden of disease and injury attributable to 67 risk factors and risk factor clusters in 21 regions, 1990–2010: a systematic analysis for the Global Burden of Disease Study 2010

          The Lancet, 380(9859), 2224-2260
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            DisGeNET: a comprehensive platform integrating information on human disease-associated genes and variants

            The information about the genetic basis of human diseases lies at the heart of precision medicine and drug discovery. However, to realize its full potential to support these goals, several problems, such as fragmentation, heterogeneity, availability and different conceptualization of the data must be overcome. To provide the community with a resource free of these hurdles, we have developed DisGeNET (http://www.disgenet.org), one of the largest available collections of genes and variants involved in human diseases. DisGeNET integrates data from expert curated repositories, GWAS catalogues, animal models and the scientific literature. DisGeNET data are homogeneously annotated with controlled vocabularies and community-driven ontologies. Additionally, several original metrics are provided to assist the prioritization of genotype–phenotype relationships. The information is accessible through a web interface, a Cytoscape App, an RDF SPARQL endpoint, scripts in several programming languages and an R package. DisGeNET is a versatile platform that can be used for different research purposes including the investigation of the molecular underpinnings of specific human diseases and their comorbidities, the analysis of the properties of disease genes, the generation of hypothesis on drug therapeutic action and drug adverse effects, the validation of computationally predicted disease genes and the evaluation of text-mining methods performance.
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              Effects of cold weather on mortality: results from 15 European cities within the PHEWE project.

              Weather-related health effects have attracted renewed interest because of the observed and predicted climate change. The authors studied the short-term effects of cold weather on mortality in 15 European cities. The effects of minimum apparent temperature on cause- and age-specific daily mortality were assessed for the cold season (October-March) by using data from 1990-2000. For city-specific analysis, the authors used Poisson regression and distributed lag models, controlling for potential confounders. Meta-regression models summarized the results and explored heterogeneity. A 1 degrees C decrease in temperature was associated with a 1.35% (95% confidence interval (CI): 1.16, 1.53) increase in the daily number of total natural deaths and a 1.72% (95% CI: 1.44, 2.01), 3.30% (95% CI: 2.61, 3.99), and 1.25% (95% CI: 0.77, 1.73) increase in cardiovascular, respiratory, and cerebrovascular deaths, respectively. The increase was greater for the older age groups. The cold effect was found to be greater in warmer (southern) cities and persisted up to 23 days, with no evidence of mortality displacement. Cold-related mortality is an important public health problem across Europe. It should not be underestimated by public health authorities because of the recent focus on heat-wave episodes.
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                Author and article information

                Contributors
                laura.pergoli@unimi.it
                laura.cantone@unimi.it
                chiara.favero@unimi.it
                laura.angelici@unimi.it
                simona.iodice@unimi.it
                eva.pinatel@itb.cnr.it
                mirjam.hoxha@unimi.it
                laura.dioni@unimi.it
                marilena.letizia@studenti.unimi.it
                benedetta.albetti@unimi.it
                letizia.tantini@unimi.it
                rotafederica@gmail.com
                pieralberto.bertazzi@unimi.it
                amtirel@tin.it
                vincenza.dolo@univaq.it
                andrea.cattaneo@uninsubria.it
                luisella.vigna@policlinico.mi.it
                cristina.battaglia@unimi.it
                michele.carugno@unimi.it
                matteo.bonzini@unimi.it
                angela.pesatori@unimi.it
                +39 0250320127 , valentina.bollati@unimi.it
                Journal
                Part Fibre Toxicol
                Part Fibre Toxicol
                Particle and Fibre Toxicology
                BioMed Central (London )
                1743-8977
                24 August 2017
                24 August 2017
                2017
                : 14
                : 32
                Affiliations
                [1 ]ISNI 0000 0004 1757 2822, GRID grid.4708.b, EPIGET LAB, Department of Clinical Sciences and Community Health, , Università degli Studi di Milano, ; Via san Barnaba 8, 20122 Milan, Italy
                [2 ]ISNI 0000 0004 1757 8749, GRID grid.414818.0, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Unit of Occupational Medicine, ; Milan, Italy
                [3 ]ISNI 0000 0001 1940 4177, GRID grid.5326.2, Institute for Biomedical Technologies (ITB), , National Research Council (CNR), ; Segrate, Milan, Italy
                [4 ]ISNI 0000 0004 1757 2611, GRID grid.158820.6, Department of Life, Health and Environmental Sciences, , University of L’Aquila, ; L’Aquila, Italy
                [5 ]ISNI 0000000121724807, GRID grid.18147.3b, Department of Science and High Technology, , University of Insubria, ; Como, Italy
                [6 ]ISNI 0000 0004 1757 2822, GRID grid.4708.b, Department of Medical Biotechnology and Translational Medicine, , Università degli Studi di Milano, ; 20129 Milan, Italy
                Author information
                http://orcid.org/0000-0002-0370-9598
                Article
                214
                10.1186/s12989-017-0214-4
                5594543
                28899404
                260f933e-e990-4ffa-84b1-d0bba4270a63
                © The Author(s). 2017

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 9 May 2017
                : 16 August 2017
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100011199, EU Programme “Ideas”, European Research Council;
                Award ID: ERC-2011-StG 282413
                Award Recipient :
                Categories
                Research
                Custom metadata
                © The Author(s) 2017

                Toxicology
                air pollution,extracellular vesicles,micrornas,fibrinogen,cardiovascular disease
                Toxicology
                air pollution, extracellular vesicles, micrornas, fibrinogen, cardiovascular disease

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