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L-Kynurenine-induced apoptosis in human NK cells is mediated by reactive oxygen species

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dc.contributor.authorSong, Hyunkeun-
dc.contributor.authorPark, Hyunjin-
dc.contributor.authorKim, Yeong-Seok-
dc.contributor.authorKim, Kwang Dong-
dc.contributor.authorLee, Hyun-Kyung-
dc.contributor.authorCho, Dae-Ho-
dc.contributor.authorYang, Jae-Wook-
dc.contributor.authorHur, Dae Young-
dc.date.accessioned2022-12-27T03:02:32Z-
dc.date.available2022-12-27T03:02:32Z-
dc.date.issued2011-08-
dc.identifier.issn1567-5769-
dc.identifier.issn1878-1705-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/23629-
dc.description.abstractRecent studies have shown that indoleamine 2,3-dioxygenase (IDO) plays a pivotal role in the modulation of immune response against tumor and virus infection. Here we demonstrate the pro-apoptotic effect of L-kynurenine, a tryptophan catabolite of IDO, on human NK cell line, NK92 MI. Treatment with L-kynurenine dose-dependently induced growth inhibition and apoptosis in NK92 MI cells. Treatment with the antioxidant NAC completely protected cells from L-kynurenine-induced apoptosis. Moreover, we found that treatment with Z-VAD-fmk and ZB4 slightly inhibited L-kynurenine-induced apoptosis, suggesting that L-kynurenine-induced apoptosis in NK cells occurs primarily through an ROS mediated pathway. We observed that the presence of NAC blocks cytochrome c release and activation of caspase-3 during L-kynurenine-induced apoptosis. Overall, we conclude that L-kynurenine resulting from 100 can cause cell death via ROS pathway in NK cells. Our findings provide a new insight into the interaction between NK cells and IDO positive cancer cells in regulating immune responses. Crown Copyright (C) 2011 Published by Elsevier B.V. All rights reserved.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER SCIENCE BV-
dc.titleL-Kynurenine-induced apoptosis in human NK cells is mediated by reactive oxygen species-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1016/j.intimp.2011.02.005-
dc.identifier.scopusid2-s2.0-84860388908-
dc.identifier.wosid000293723400005-
dc.identifier.bibliographicCitationINTERNATIONAL IMMUNOPHARMACOLOGY, v.11, no.8, pp 932 - 938-
dc.citation.titleINTERNATIONAL IMMUNOPHARMACOLOGY-
dc.citation.volume11-
dc.citation.number8-
dc.citation.startPage932-
dc.citation.endPage938-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusNATURAL-KILLER-CELLS-
dc.subject.keywordPlusINDOLEAMINE 2,3-DIOXYGENASE-
dc.subject.keywordPlusT-CELL-
dc.subject.keywordPlusTRYPTOPHAN CATABOLISM-
dc.subject.keywordPlusDENDRITIC CELLS-
dc.subject.keywordPlusINTERFERON-GAMMA-
dc.subject.keywordPlusINHIBITION-
dc.subject.keywordPlusPROLIFERATION-
dc.subject.keywordPlusMETABOLITES-
dc.subject.keywordPlusCANCER-
dc.subject.keywordAuthorNK cell-
dc.subject.keywordAuthorROS-
dc.subject.keywordAuthorIDO-
dc.subject.keywordAuthorL-Kynurenine-
dc.subject.keywordAuthorApoptosis-
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