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dc.contributor.authorMourabit, S
dc.contributor.authorFitzgerald, JA
dc.contributor.authorEllis, RP
dc.contributor.authorTakesono, A
dc.contributor.authorPorteus, CS
dc.contributor.authorTrznadel, M
dc.contributor.authorMetz, J
dc.contributor.authorWinter, MJ
dc.contributor.authorKudoh, T
dc.contributor.authorTyler, CR
dc.date.accessioned2019-11-26T08:20:56Z
dc.date.issued2019-10-20
dc.description.abstractBackground: Reactive oxygen species (ROS) arise as a result from, and are essential in, numerous cellular processes. ROS, however, are highly reactive and if left unneutralised by endogenous antioxidant systems, can result in extensive cellular damage and/or pathogenesis. In addition, exposure to a wide range of environmental stressors can also result in surplus ROS production leading to oxidative stress (OS) and downstream tissue toxicity. Objectives: Our aim was to produce a stable transgenic zebrafish line, unrestricted by tissue-specific gene regulation, which was capable of providing a whole organismal, real-time read-out of tissue-specific OS following exposure to a wide range of OS-inducing environmental contaminants and conditions. This model could, therefore, serve as a sensitive and specific mechanistic in vivo biomarker for all environmental conditions that result in OS. Methods: To achieve this aim, we exploited the pivotal role of the electrophile response element (EpRE) as a globally-acting master regulator of the cellular response to OS. To test tissue specificity and quantitative capacity, we selected a range of chemical contaminants known to induce OS in specific organs or tissues, and assessed dose-responsiveness in each using microscopic measures of mCherry fluorescence intensity. Results: We produced the first stable transgenic zebrafish line Tg (3EpRE:hsp70:mCherry) with high sensitivity for the detection of cellular RedOx imbalances, in vivo in near-real time. We applied this new model to quantify OS after exposure to a range of environmental conditions with high resolution and provided quantification both of compound- and tissue-specific ROS-induced toxicity. Discussion: Our model has an extremely diverse range of potential applications not only for biomonitoring of toxicants in aqueous environments, but also in biomedicine for identifying ROS-mediated mechanisms involved in the progression of a number of important human diseases, including cancer.en_GB
dc.description.sponsorshipNatural Environmental Research Councilen_GB
dc.description.sponsorshipEuropean Unionen_GB
dc.identifier.citationVol. 133, Part A, 105138en_GB
dc.identifier.doi10.1016/j.envint.2019.105138
dc.identifier.grantnumberNE/L007371/1en_GB
dc.identifier.urihttp://hdl.handle.net/10871/39789
dc.language.isoenen_GB
dc.publisherElsevieren_GB
dc.rights© 2019 Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/BY-NC-ND/4.0/).en_GB
dc.subjectOxidative stressen_GB
dc.subjectZebrafishen_GB
dc.subjectToxicantsen_GB
dc.subjectBiosensoren_GB
dc.titleNew insights into organ-specific oxidative stress mechanisms using a novel biosensor zebrafishen_GB
dc.typeArticleen_GB
dc.date.available2019-11-26T08:20:56Z
dc.identifier.issn0160-4120
dc.descriptionThis is the final version. Available from Elsevier via the DOI in this record. en_GB
dc.identifier.journalEnvironment Internationalen_GB
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/en_GB
dcterms.dateAccepted2019-08-27
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2019-10-20
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2019-11-26T08:17:24Z
refterms.versionFCDVoR
refterms.dateFOA2019-11-26T08:20:59Z
refterms.panelAen_GB


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© 2019 Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license
(http://creativecommons.org/licenses/BY-NC-ND/4.0/).
Except where otherwise noted, this item's licence is described as © 2019 Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/BY-NC-ND/4.0/).