Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/139366
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dc.contributor.authorGautam, Archanaen_US
dc.contributor.authorRakshit, Moumitaen_US
dc.contributor.authorNguyen, Kim Trucen_US
dc.contributor.authorKathawala, Mustafa Hussainen_US
dc.contributor.authorNguyen, Luong Thi Hienen_US
dc.contributor.authorTay, Chor Yongen_US
dc.contributor.authorWong, Estheren_US
dc.contributor.authorNg, Kee Woeien_US
dc.date.accessioned2020-05-19T05:18:51Z-
dc.date.available2020-05-19T05:18:51Z-
dc.date.issued2019-
dc.identifier.citationGautam, A., Rakshit, M., Nguyen, K. T., Kathawala, M. H., Nguyen, L. T. H., Tay, C. Y., . . ., Ng, K. W. (2019). Understanding the implications of engineered nanoparticle induced autophagy in human epidermal keratinocytes in vitro. NanoImpact, 15, 100177-. doi:10.1016/j.impact.2019.100177en_US
dc.identifier.issn2452-0748en_US
dc.identifier.urihttps://hdl.handle.net/10356/139366-
dc.description.abstractEngineered nanoparticles (NPs) such as TiO2 and ZnO are key UV-blocking ingredients in sunscreens. While toxicological risks of applying these materials are generally regarded as low due to minute levels of penetration across the skin, our understanding of the physiological influence of potential cell-nanoparticle interactions in the skin is limited. This study plugs the current knowledge gap by profiling TiO2 and ZnO NP interaction with primary human epidermal keratinocytes, based on potential levels of NP penetration across the skin. Specific attention was given to profiling real-life relevant levels of exposure, and accurate dosimetry measurements in vitro. ZnO was expectedly more cytotoxic than TiO2. Although both NPs generated Reactive Oxygen Species (ROS) and Mitochondrial Superoxide (MSO) within 4 h exposure to sub-lethal concentrations, ZnO induction of these oxidative stress markers increased much more significantly after 24 h exposure. Exposure to increasing NP concentrations increased autophagy induction along with activation of inflammatory responses in the keratinocytes, primarily through the TRAF6-mediated pathway. Sustained induction of autophagy led to degradation of TRAF6 and, only in the case of TiO2, reduced NF-κB activation. This pro-survival mode of autophagy induction provides further insights into the on-going debate on the use of these NPs in consumer products.en_US
dc.language.isoenen_US
dc.relation.ispartofNanoImpacten_US
dc.rights© 2019 Elsevier B.V. All rights reserved. This paper was published in NanoImpact and is made available with permission of Elsevier B.V.en_US
dc.subjectScience::Biological sciencesen_US
dc.titleUnderstanding the implications of engineered nanoparticle induced autophagy in human epidermal keratinocytes in vitroen_US
dc.typeJournal Articleen
dc.contributor.schoolSchool of Materials Science & Engineeringen_US
dc.contributor.schoolSchool of Biological Sciencesen_US
dc.contributor.organizationEnvironmental Chemistry and Materials Centreen_US
dc.contributor.researchNanyang Environment and Water Research Instituteen_US
dc.identifier.doi10.1016/j.impact.2019.100177-
dc.description.versionAccepted versionen_US
dc.identifier.scopus2-s2.0-85068852421-
dc.identifier.volume15en_US
dc.subject.keywordsKeratinocytesen_US
dc.subject.keywordsSunscreenen_US
item.grantfulltextopen-
item.fulltextWith Fulltext-
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