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dc.contributor.authorIlves, M
dc.contributor.authorKinaret, PAS
dc.contributor.authorNdika, J
dc.contributor.authorKarisola, P
dc.contributor.authorMarwah, V
dc.contributor.authorFortino, V
dc.contributor.authorFedutik, Y
dc.contributor.authorCorreia, M
dc.contributor.authorEhrlich, N
dc.contributor.authorLoeschner, K
dc.contributor.authorBesinis, A
dc.contributor.authorVassallo, J
dc.contributor.authorHandy, RD
dc.contributor.authorWolff, H
dc.contributor.authorSavolainen, K
dc.contributor.authorGreco, D
dc.contributor.authorAlenius, H
dc.date.accessioned2019-09-02T08:52:42Z
dc.date.issued2019-07-05
dc.identifier.issn1743-8977
dc.identifier.issn1743-8977
dc.identifier.other28
dc.identifier.urihttp://hdl.handle.net/10026.1/14846
dc.description.abstract

BACKGROUND: Copper oxide (CuO) nanomaterials are used in a wide range of industrial and commercial applications. These materials can be hazardous, especially if they are inhaled. As a result, the pulmonary effects of CuO nanomaterials have been studied in healthy subjects but limited knowledge exists today about their effects on lungs with allergic airway inflammation (AAI). The objective of this study was to investigate how pristine CuO modulates allergic lung inflammation and whether surface modifications can influence its reactivity. CuO and its carboxylated (CuO COOH), methylaminated (CuO NH3) and PEGylated (CuO PEG) derivatives were administered here on four consecutive days via oropharyngeal aspiration in a mouse model of AAI. Standard genome-wide gene expression profiling as well as conventional histopathological and immunological methods were used to investigate the modulatory effects of the nanomaterials on both healthy and compromised immune system. RESULTS: Our data demonstrates that although CuO materials did not considerably influence hallmarks of allergic airway inflammation, the materials exacerbated the existing lung inflammation by eliciting dramatic pulmonary neutrophilia. Transcriptomic analysis showed that CuO, CuO COOH and CuO NH3 commonly enriched neutrophil-related biological processes, especially in healthy mice. In sharp contrast, CuO PEG had a significantly lower potential in triggering changes in lungs of healthy and allergic mice revealing that surface PEGylation suppresses the effects triggered by the pristine material. CONCLUSIONS: CuO as well as its functionalized forms worsen allergic airway inflammation by causing neutrophilia in the lungs, however, our results also show that surface PEGylation can be a promising approach for inhibiting the effects of pristine CuO. Our study provides information for health and safety assessment of modified CuO materials, and it can be useful in the development of nanomedical applications.

dc.format.extent28-
dc.format.mediumElectronic
dc.languageen
dc.language.isoen
dc.publisherBMC
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectCuO
dc.subjectEngineered nanomaterial
dc.subjectHealth effects
dc.subjectInflammation
dc.subjectAsthma
dc.subjectAllergic airway inflammation
dc.subjectRisk assessment
dc.titleSurface PEGylation suppresses pulmonary effects of CuO in allergen-induced lung inflammation
dc.typejournal-article
dc.typeArticle
plymouth.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/31277695
plymouth.issue1
plymouth.volume16
plymouth.publication-statusPublished
plymouth.journalParticle and Fibre Toxicology
dc.identifier.doi10.1186/s12989-019-0309-1
plymouth.organisational-group/Plymouth
plymouth.organisational-group/Plymouth/Faculty of Science and Engineering
plymouth.organisational-group/Plymouth/Faculty of Science and Engineering/School of Biological and Marine Sciences
plymouth.organisational-group/Plymouth/Faculty of Science and Engineering/School of Engineering, Computing and Mathematics
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA06 Agriculture, Veterinary and Food Science
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA12 Engineering
plymouth.organisational-group/Plymouth/Research Groups
plymouth.organisational-group/Plymouth/Research Groups/Marine Institute
plymouth.organisational-group/Plymouth/Users by role
plymouth.organisational-group/Plymouth/Users by role/Academics
dc.publisher.placeEngland
dcterms.dateAccepted2019-06-04
dc.rights.embargodate2019-9-11
dc.identifier.eissn1743-8977
dc.rights.embargoperiodNot known
rioxxterms.versionVersion of Record
rioxxterms.versionofrecord10.1186/s12989-019-0309-1
rioxxterms.licenseref.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
rioxxterms.licenseref.startdate2019-07-05
rioxxterms.typeJournal Article/Review
plymouth.funderNANOSOLUTIONS Biological Foundation for the Safety Classification of Engineered Nanomaterials (ENM): Systems Biology Approaches to Understand::European Commission FP7


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