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dc.contributor.authorRodríguez Barucg, Quentin
dc.contributor.authorGarcía, Ángel A.
dc.contributor.authorGarcía Merino, Belén 
dc.contributor.authorAkinmola, Tomilayo
dc.contributor.authorOkotie-Eboh, Temisanren
dc.contributor.authorFrancis, Thomas
dc.contributor.authorBringas Elizalde, Eugenio 
dc.contributor.authorOrtiz Uribe, Inmaculada 
dc.contributor.authorWade, Mark A.
dc.contributor.authorDowle, Adam
dc.contributor.authorJoyce, Domino A.
dc.contributor.authorHardman, Matthew J.
dc.contributor.authorWilkinson, Holly N.
dc.contributor.authorBeltrán Álvarez, Pedro
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2024-10-02T16:31:35Z
dc.date.available2024-10-02T16:31:35Z
dc.date.issued2024-12-01
dc.identifier.issn0269-7491
dc.identifier.issn1873-6424
dc.identifier.urihttps://hdl.handle.net/10902/34037
dc.description.abstractThis study investigates the effects of environmentally-relevant concentrations of fluoxetine (FLX, commercial name: Prozac) on wound healing. Pollution of water systems with pharmaceutical and personal care products, including antidepressants such as FLX and other selective serotonin reuptake inhibitors, is a growing environmental concern. Environmentally-relevant FLX concentrations are known to impact physiological functions and behaviour of aquatic animals, however, the effects of exposure on humans are currently unknown. Using a combination of human skin biopsies and a human keratinocyte cell line, we show that exposure to environmental FLX promotes wound closure. We show dose-dependent increases in wound closure with FLX concentrations from 125 ng/l. Using several –omics and pharmaceutical approaches, we demonstrate that the mechanisms underlying enhanced wound closure are increased cell proliferation and serotonin signalling. Transcriptomic analysis revealed 350 differentially expressed genes after exposure. Downregulated genes were enriched in pathways related to mitochondrial function and metabolism, while upregulated genes were associated with cell proliferation and tissue morphogenesis. Kinase profiling showed altered phosphorylation of kinases linked to the MAPK pathway. Consistent with this, phosphoproteomic analyses identified 235 differentially phosphorylated proteins after exposure, with enriched GO terms related to cell cycle, division, and protein biosynthesis. Treatment of skin biopsies and keratinocytes with ketanserin, a serotonin receptor antagonist, reversed the increase in wound closure observed upon exposure. These findings collectively show that exposure to environmental FLX promotes wound healing through modulating serotonin signalling, gene expression and protein phosphorylation, leading to enhanced cell proliferation. Our results justify a transition from the study of behavioural effects of environmental FLX in aquatic animals to the investigation of effects of exposure on wound healing in aquatic and terrestrial animals, including direct impacts on human health.es_ES
dc.description.sponsorshipQRB acknowledges a ‘Happy Chemical’ PhD studentship funded by the University of Hull. BGM would also like to express her gratitude to the Spanish Ministry of Science, Innovation and Universities for the FPI predoctoral contract PRE2019–089339 and to the University of Cantabria for the predoctoral mobility grant Erasmus+ nº 2021-1-ES01-KA131-HED-000005117. The York Centre of Excellence in Mass Spectrometry was created thanks to a major capital investment through Science City York, supported by Yorkshire Forward with funds from the Northern Way Initiative, and subsequent support from EPSRC (EP/K039660/1; EP/M028127/1).es_ES
dc.format.extent14 p.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsAttribution 4.0 Internationales_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourceEnvironmental Pollution, 2024, 362, 124952es_ES
dc.subject.otherFluoxetinees_ES
dc.subject.otherKeratinocytees_ES
dc.subject.otherSerotonines_ES
dc.subject.otherSkines_ES
dc.subject.otherWound healinges_ES
dc.titleEnvironmental fluoxetine promotes skin cell proliferation and wound healinges_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1016/j.envpol.2024.124952es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1016/j.envpol.2024.124952
dc.type.versionpublishedVersiones_ES


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Attribution 4.0 InternationalExcepto si se señala otra cosa, la licencia del ítem se describe como Attribution 4.0 International