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dc.contributor.author윤태현-
dc.date.accessioned2021-04-08T08:01:03Z-
dc.date.available2021-04-08T08:01:03Z-
dc.date.issued2020-02-
dc.identifier.citationENVIRONMENTAL SCIENCE-NANO, v. 7, no. 4, page. 1102-1114en_US
dc.identifier.issn2051-8153-
dc.identifier.issn2051-8161-
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2020/EN/C9EN01104H#!divAbstract-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/161302-
dc.description.abstractIn recent years, there have been remarkable efforts to examine and understand the adverse effects of nanoparticles (NPs) on the environment and human health, not only qualitatively but also quantitatively. Mass cytometry has been developed for high-dimensional single-cell analyses and used to quantify the cellular association of inorganic NPs. Here, we have applied this novel technique to investigate the heterogeneity in cellular association and cytotoxicity of polyvinylpyrrolidone-coated silver nanoparticles with diameters of 10 nm and 20 nm in primary human immune cells. Our results revealed the cell-type-dependent heterogeneity in which AgNPs showed higher affinity to phagocytic cells like monocytes and dendritic cells than to other immune cell types. Upon exposure to AgNPs, these cells exhibited complex pro-inflammatory and pro-apoptotic responses, such as I kappa B alpha degradation, STAT1 phosphorylation and caspase-7 activation. Quantitative analyses of the single-cell dose-response relationship between the cellular AgNP association and signalling activities further revealed heterogeneity even within a monocyte population. The majority of cells belonged to the 'low affinity' subset, which showed a positive AgNP dose-cisplatin uptake (i.e. viability loss) correlation, as opposed to the remaining cells which belonged to the 'high affinity' subset and had an insignificant relationship between the cell-associated AgNP amount and cisplatin uptake/viability loss level. These subsets were distinctly responsive to the cellular AgNP content, as they showed different levels of signalling proteins such as I kappa B alpha, STAT1 and caspase-7. Our study can be helpful for further understanding the heterogeneous nature of cell-NP interactions and development of dose-response models at the single-cell level for various NPs, which will provide key information for the safe use of nanomaterials in biomedical applications.en_US
dc.description.sponsorshipThis research was supported by the Bio & Medical Technology Development Program of the National Research Foundation of Korea funded by the Ministry of Science & ICT (grant agreement no. 2017M3A9G8084539) and by the Korea Basic Science Institute (National Research Facilities and Equipment Center) funded by the Ministry of Education (grant agreement no. 2019R1A6C1030014). Mass cytometry experiments were performed on the Helios instrument at the Biotechnology Research Centre in POSTECH, Republic of Korea. The authors would like to thank Prof. Young Tae Chang and Dr. Jong Jin Kim (POSTECH, Republic of Korea) for providing access to the Helios instrument and helping with its operation. The authors would also like to thank Prof. Incheol Shin (Hanyang University, Republic of Korea) for his comments on this manuscript.en_US
dc.language.isoenen_US
dc.publisherROYAL SOC CHEMISTRYen_US
dc.subjectSINGLE-CELLen_US
dc.subjectGOLD NANOPARTICLESen_US
dc.subjectLIGHT SCATTERen_US
dc.subjectIN-VITROen_US
dc.subjectQUANTIFICATIONen_US
dc.subjectLEVELen_US
dc.subjectRESPONSESen_US
dc.subjectGENOTOXICITYen_US
dc.subjectFLUORESCENCEen_US
dc.subjectEXOCYTOSISen_US
dc.titleMass cytometric study on the heterogeneity in cellular association and cytotoxicity of silver nanoparticles in primary human immune cellsen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c9en01104h-
dc.relation.page1-13-
dc.relation.journalENVIRONMENTAL SCIENCE-NANO-
dc.contributor.googleauthorHa, My Kieu-
dc.contributor.googleauthorChoi, Jang-Sik-
dc.contributor.googleauthorKwon, Sook Jin-
dc.contributor.googleauthorSong, Jaewoo-
dc.contributor.googleauthorLee, Yangsoon-
dc.contributor.googleauthorKim, Young-Eun-
dc.contributor.googleauthorYoon, Tae Hyun-
dc.relation.code2020049740-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF NATURAL SCIENCES[S]-
dc.sector.departmentDEPARTMENT OF CHEMISTRY-
dc.identifier.pidtaeyoon-
dc.identifier.orcidhttps://orcid.org/0000-0002-2743-6360-
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COLLEGE OF NATURAL SCIENCES[S](자연과학대학) > CHEMISTRY(화학과) > Articles
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