Two distinct cellular pathways leading to endothelial cell cytotoxicity by silica nanoparticle size

Cited 34 time in scopus
Metadata Downloads

Full metadata record

DC FieldValueLanguage
dc.contributor.authorKyungmin Lee-
dc.contributor.authorJangwook Lee-
dc.contributor.authorM Kwak-
dc.contributor.authorYoung Lai Cho-
dc.contributor.authorByungtae Hwang-
dc.contributor.authorMin Ji Cho-
dc.contributor.authorNa Geum Lee-
dc.contributor.authorJongjin Park-
dc.contributor.authorSang Hyun Lee-
dc.contributor.authorJong Gil Park-
dc.contributor.authorYeon-Gu Kim-
dc.contributor.authorJang Seong Kim-
dc.contributor.authorTae Su Han-
dc.contributor.authorHyun Soo Cho-
dc.contributor.authorYoung-Jun Park-
dc.contributor.authorSeon-Jin Lee-
dc.contributor.authorHee Gu Lee-
dc.contributor.authorWon Kon-Kim-
dc.contributor.authorI C Jeung-
dc.contributor.authorN W Song-
dc.contributor.authorKwang-Hee Bae-
dc.contributor.authorJeong Ki Min-
dc.date.accessioned2019-04-09T16:30:12Z-
dc.date.available2019-04-09T16:30:12Z-
dc.date.issued2019-
dc.identifier.issn1477-3155-
dc.identifier.uri10.1186/s12951-019-0456-4ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/18427-
dc.description.abstractBACKGROUND: Silica nanoparticles (SiNPs) are widely used for biosensing and diagnostics, and for the targeted delivery of therapeutic agents. Safety concerns about the biomedical and clinical applications of SiNPs have been raised, necessitating analysis of the effects of their intrinsic properties, such as sizes, shapes, and surface physicochemical characteristics, on human health to minimize risk in biomedical applications. In particular, SiNP size-associated toxicological effects, and the underlying molecular mechanisms in the vascular endothelium remain unclear. This study aimed to elucidate the detailed mechanisms underlying the cellular response to exposure to trace amounts of SiNPs and to determine applicable size criteria for biomedical application. METHODS: To clarify whether these SiNP-mediated cytotoxicity due to induction of apoptosis or necrosis, human ECs were treated with SiNPs of four different non-overlapping sizes under low serum-containing condition, stained with annexin V and propidium iodide (PI), and subjected to flow cytometric analysis (FACS). Two types of cell death mechanisms were assessed in terms of production of reactive oxygen species (ROS), endoplasmic reticulum (ER) stress induction, and autophagy activity. RESULTS: Spherical SiNPs had a diameter of 21.8 nm; this was further increased to 31.4, 42.9, and 56.7 nm. Hence, we investigated these effects in human endothelial cells (ECs) treated with these nanoparticles under overlap- or agglomerate-free conditions. The 20-nm SiNPs, but not SiNPs of other sizes, significantly induced apoptosis and necrosis. Surprisingly, the two types of cell death occurred independently and through different mechanisms. Apoptotic cell death resulted from ROS-mediated ER stress. Furthermore, autophagy-mediated necrotic cell death was induced through the PI3K/AKT/eNOS signaling axis. Together, the present results indicate that SiNPs within a diameter of<20-nm pose greater risks to cells in terms of cytotoxic effects. CONCLUSION: These data provide novel insights into the size-dependence of the cytotoxic effects of silica nanoparticles and the underlying molecular mechanisms. The findings are expected to inform the applicable size range of SiNPs to ensure their safety in biomedical and clinical applications.-
dc.publisherSpringer-BMC-
dc.titleTwo distinct cellular pathways leading to endothelial cell cytotoxicity by silica nanoparticle size-
dc.title.alternativeTwo distinct cellular pathways leading to endothelial cell cytotoxicity by silica nanoparticle size-
dc.typeArticle-
dc.citation.titleJournal of Nanobiotechnology-
dc.citation.number0-
dc.citation.endPage24-
dc.citation.startPage24-
dc.citation.volume17-
dc.contributor.affiliatedAuthorKyungmin Lee-
dc.contributor.affiliatedAuthorJangwook Lee-
dc.contributor.affiliatedAuthorYoung Lai Cho-
dc.contributor.affiliatedAuthorByungtae Hwang-
dc.contributor.affiliatedAuthorMin Ji Cho-
dc.contributor.affiliatedAuthorNa Geum Lee-
dc.contributor.affiliatedAuthorJongjin Park-
dc.contributor.affiliatedAuthorSang Hyun Lee-
dc.contributor.affiliatedAuthorJong Gil Park-
dc.contributor.affiliatedAuthorYeon-Gu Kim-
dc.contributor.affiliatedAuthorJang Seong Kim-
dc.contributor.affiliatedAuthorTae Su Han-
dc.contributor.affiliatedAuthorHyun Soo Cho-
dc.contributor.affiliatedAuthorYoung-Jun Park-
dc.contributor.affiliatedAuthorSeon-Jin Lee-
dc.contributor.affiliatedAuthorHee Gu Lee-
dc.contributor.affiliatedAuthorWon Kon-Kim-
dc.contributor.affiliatedAuthorKwang-Hee Bae-
dc.contributor.affiliatedAuthorJeong Ki Min-
dc.contributor.alternativeName이경민-
dc.contributor.alternativeName이장욱-
dc.contributor.alternativeName곽민정-
dc.contributor.alternativeName조영래-
dc.contributor.alternativeName황병태-
dc.contributor.alternativeName조민지-
dc.contributor.alternativeName이나금-
dc.contributor.alternativeName박종진-
dc.contributor.alternativeName이상현-
dc.contributor.alternativeName박종길-
dc.contributor.alternativeName김연구-
dc.contributor.alternativeName김장성-
dc.contributor.alternativeName한태수-
dc.contributor.alternativeName조현수-
dc.contributor.alternativeName박영준-
dc.contributor.alternativeName이선진-
dc.contributor.alternativeName이희구-
dc.contributor.alternativeName김원곤-
dc.contributor.alternativeName정인철-
dc.contributor.alternativeName송남웅-
dc.contributor.alternativeName배광희-
dc.contributor.alternativeName민정기-
dc.identifier.bibliographicCitationJournal of Nanobiotechnology, vol. 17, pp. 24-24-
dc.identifier.doi10.1186/s12951-019-0456-4-
dc.subject.keywordApoptosis-
dc.subject.keywordAutophagy-
dc.subject.keywordNecroptosis-
dc.subject.keywordROS-
dc.subject.keywordSilica nanoparticles-
dc.subject.localapoptosis-
dc.subject.localApoptosis-
dc.subject.localautophagy-
dc.subject.localAutophagy-
dc.subject.localNecroptosis-
dc.subject.localnecroptosis-
dc.subject.localReactive oxidative species-
dc.subject.localReactive oxygen species(ROS)-
dc.subject.localReactive oxygen species-
dc.subject.localReactive Oxygen Species (ROS)-
dc.subject.localReactive Oxygen Species-
dc.subject.localROS-
dc.subject.localReactive oxygen species (ROS)-
dc.subject.localreactive oxygen species-
dc.subject.localreactive oxygen species (ROS)-
dc.subject.localSilica nanoparticle-
dc.subject.localsilica nanoparticles-
dc.subject.localSilica nanoparticles-
dc.subject.localsilica nanoparticle-
dc.description.journalClassY-
Appears in Collections:
Division of Biomedical Research > Biotherapeutics Translational Research Center > 1. Journal Articles
Division of Biomedical Research > Metabolic Regulation Research Center > 1. Journal Articles
Division of Research on National Challenges > Stem Cell Convergenece Research Center > 1. Journal Articles
Division of Research on National Challenges > Environmental diseases research center > 1. Journal Articles
Division of Biomedical Research > Immunotherapy Research Center > 1. Journal Articles
Files in This Item:

Items in OpenAccess@KRIBB are protected by copyright, with all rights reserved, unless otherwise indicated.