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Evaluating the genotoxicity of cellulose nanofibrils in a co-culture of human lung epithelial cells and monocyte-derived macrophages

dc.contributor.authorVentura, Célia
dc.contributor.authorLourenço, Ana Filipa
dc.contributor.authorSousa-Uva, António
dc.contributor.authorFerreira, Paulo J.T.
dc.contributor.authorSilva, Maria João
dc.date.accessioned2019-02-20T10:37:03Z
dc.date.available2019-02-20T10:37:03Z
dc.date.issued2018-07
dc.description.abstractCellulose nanofibrils (CNF) are manufactured nanofibres that hold impressive expectations in forest, food, pharmaceutical, and biomedical industries. CNF production and applications are leading to an increased human exposure and thereby it is of utmost importance to assess its safety to health. In this study, we screened the cytotoxic, immunotoxic and genotoxic effects of a CNF produced by TEMPO-mediated oxidation of an industrial bleached Eucalyptus globulus kraft pulp on a co-culture of lung epithelial alveolar (A549) cells and monocyte-derived macrophages (THP-1 cells). The results indicated that low CNF concentrations can stimulate A549 cells proliferation, whereas higher concentrations are moderately toxic. Moreover, no proinflammatory cytokine IL-1β was detected in the co-culture medium suggesting no immunotoxicity. Although CNF treatment did not induce sizable levels of DNA damage in A549 cells, it leaded to micronuclei formation at 1.5 and 3 μg/cm2. These findings suggest that this type of CNF is genotoxic through aneugenic or clastogenic mechanisms. Noteworthy, cell overgrowth and genotoxicity, which are events relevant for cell malignant transformation, were observed at low CNF concentration levels, which are more realistic and relevant for human exposure, e.g., in occupational settings.pt_PT
dc.description.sponsorshipThis research was co-funded through UID/BIM/00009/2013, Centre for Toxicogenomics and Human Health (ToxOmics), and SFRH/BDE/ 108095/2015, from the Foundation for Science and Technology, Portugalpt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationToxicol Lett. 2018 Jul;291:173-183. doi: 10.1016/j.toxlet.2018.04.013. Epub 2018 Apr 18.pt_PT
dc.identifier.doidoi.org/10.1016/j.toxlet.2018.04.013pt_PT
dc.identifier.issn0378-4274
dc.identifier.urihttp://hdl.handle.net/10400.18/5909
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherElsevier/EUROTOXpt_PT
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S0378427418301504?via%3Dihubpt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectCellulose Nanofibrilspt_PT
dc.subjectSafety Assessmentpt_PT
dc.subjectImmunotoxicitypt_PT
dc.subjectComet Assaypt_PT
dc.subjectMicronucleus Assaypt_PT
dc.subjectGenotoxicidade Ambientalpt_PT
dc.titleEvaluating the genotoxicity of cellulose nanofibrils in a co-culture of human lung epithelial cells and monocyte-derived macrophagespt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/5876/UID%2FBIM%2F00009%2F2013/PT
oaire.citation.endPage183pt_PT
oaire.citation.startPage173pt_PT
oaire.citation.titleToxicology Letterspt_PT
oaire.citation.volume291pt_PT
oaire.fundingStream5876
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.embargofctPolítica editorialpt_PT
rcaap.rightsembargoedAccesspt_PT
rcaap.typearticlept_PT
relation.isProjectOfPublicatione9cc9728-4f09-4e3a-b30d-53d4429986fb
relation.isProjectOfPublication.latestForDiscoverye9cc9728-4f09-4e3a-b30d-53d4429986fb

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