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Cited 85 time in webofscience Cited 90 time in scopus
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dc.contributor.authorPark, Y-
dc.contributor.authorLee, SW-
dc.contributor.authorSung, YC-
dc.date.accessioned2016-03-31T13:11:06Z-
dc.date.available2016-03-31T13:11:06Z-
dc.date.created2009-02-28-
dc.date.issued2002-01-01-
dc.identifier.issn0022-1767-
dc.identifier.other2002-OAK-0000002398-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/19258-
dc.description.abstractCpG DNA has been recognized as a powerful stimulant of dendritic cells (DCs). In this study, we demonstrate that CpG DNA inhibits spontaneous apoptosis of DCs. CpG DNA up-regulated cellular inhibitor of apoptosis proteins (cIAPs) as well as Bcl-2 and Bcl-x(L), but down-regulated active caspase-3. Although CpG DNA activated p38 mitogen-activated protein kinase, extracellular signal-related kinase, and phosphatidylinositide-3'-OH kinase (PI3K), only the blocking of PI3K inhibited the CpG DNA-induced DC survival. Moreover, while the expression of Bcl-2 and Bel-x(L) depends on both PI3K and p38 mitogen-activated protein kinase, the up-regulation of cIAPs and the down-regulation of active caspase-3 by CpG DNA require PI3K activation, suggesting PI3K-dependent upregulation of cIAPs in the antiapoptotic activity of CpG DNA in DCs. This study indicates that CpG DNA provides a survival signal to DCs, which might be one of mechanisms by which bacterial DNA stimulates and maintains the innate immune responses.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherAMER ASSOC IMMUNOLOGISTS-
dc.relation.isPartOfJOURNAL OF IMMUNOLOGY-
dc.subjectANTIGEN-PRESENTING CELLS-
dc.subjectBACTERIAL-DNA-
dc.subjectIMMUNOSTIMULATORY DNA-
dc.subjectACTIVATION-
dc.subjectSURVIVAL-
dc.subjectMATURATION-
dc.subjectOLIGODEOXYNUCLEOTIDES-
dc.subjectINDUCTION-
dc.subjectFAMILY-
dc.subjectPLAY-
dc.titleCutting edge: CpG DNA inhibits dendritic cell apoptosis by up-regulating cellular inhibitor of apoptosis proteins through the phosphatidylinositide-3 '-OH kinase pathway-
dc.typeArticle-
dc.contributor.college생명과학과-
dc.identifier.doi10.4049/jimmunol.168.1.5-
dc.author.googlePark, Y-
dc.author.googleLee, SW-
dc.author.googleSung, YC-
dc.relation.volume168-
dc.relation.issue1-
dc.relation.startpage5-
dc.relation.lastpage8-
dc.contributor.id10053752-
dc.relation.journalJOURNAL OF IMMUNOLOGY-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationJOURNAL OF IMMUNOLOGY, v.168, no.1, pp.5 - 8-
dc.identifier.wosid000172934000002-
dc.date.tcdate2019-01-01-
dc.citation.endPage8-
dc.citation.number1-
dc.citation.startPage5-
dc.citation.titleJOURNAL OF IMMUNOLOGY-
dc.citation.volume168-
dc.contributor.affiliatedAuthorSung, YC-
dc.identifier.scopusid2-s2.0-0036134876-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc82-
dc.type.docTypeArticle-
dc.subject.keywordPlusANTIGEN-PRESENTING CELLS-
dc.subject.keywordPlusBACTERIAL-DNA-
dc.subject.keywordPlusIMMUNOSTIMULATORY DNA-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusSURVIVAL-
dc.subject.keywordPlusMATURATION-
dc.subject.keywordPlusOLIGODEOXYNUCLEOTIDES-
dc.subject.keywordPlusINDUCTION-
dc.subject.keywordPlusFAMILY-
dc.subject.keywordPlusPLAY-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaImmunology-

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