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Cited 26 time in webofscience Cited 29 time in scopus
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dc.contributor.authorLee, SW-
dc.contributor.authorPark, Y-
dc.contributor.authorEun, SY-
dc.contributor.authorMadireddi, S-
dc.contributor.authorCheroutre, H-
dc.contributor.authorCroft, M-
dc.date.accessioned2016-03-31T08:45:32Z-
dc.date.available2016-03-31T08:45:32Z-
dc.date.created2013-03-05-
dc.date.issued2012-09-15-
dc.identifier.issn0022-1767-
dc.identifier.other2012-OAK-0000026664-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/15984-
dc.description.abstractDendritic cells (DC) in the gut promote immune tolerance by expressing retinal dehydrogenase (RALDH), an enzyme that promotes retinoic acid, which aids differentiation of Foxp3(+) inducible regulatory T cells (iTreg) in the intestinal mucosa. How RALDH expression is regulated is unclear. We found that 4-1BB (CD137), a member of the TNFR family, together with CD103, marked mesenteric lymph node DC with the highest level of RALDH activity, and ligation of 4-1BB maintained RALDH expression in these gut DC. Moreover, 4-1BB signals synergized with those through TLR2 or GM-CSFR to promote RALDH activity in undifferentiated DC. Correspondingly, 4-1BB-deficient mice were impaired in their ability to generate iTreg in the GALT when exposed to oral Ag, and 4-1BB-deficient mesenteric lymph node DC displayed weak RALDH activity and were poor at promoting iTreg development. Thus, our data demonstrate a novel activity of 4-1BB in controlling RALDH expression and the regulatory activity of DC. The Journal of Immunology, 2012, 189: 2697-2701.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherThe American Association of Immunologists.-
dc.relation.isPartOfJOURNAL OF IMMUNOLOGY-
dc.subjectT-CELLS-
dc.subjectIMMUNE REGULATION-
dc.subjectVITAMIN-A-
dc.subjectACID-
dc.subjectDIFFERENTIATION-
dc.subjectRESPONSES-
dc.subjectMICROBIOTA-
dc.subjectINDUCTION-
dc.subjectSYSTEM-
dc.title4-1BB Cutting Edge: Controls Regulatory Activity in Dendritic Cells through Promoting Optimal Expression of Retinal Dehydrogenase.-
dc.typeArticle-
dc.contributor.college융합생명공학부-
dc.identifier.doi10.4049/jimmunol.1201248-
dc.author.googleLee, SW-
dc.author.googlePark, Y-
dc.author.googleEun, SY-
dc.author.googleMadireddi, S-
dc.author.googleCheroutre, H-
dc.author.googleCroft, M-
dc.relation.volume189-
dc.relation.startpage2687-
dc.relation.lastpage2701-
dc.contributor.id10113012-
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.189, no.6, pp.2687 - 2701-
dc.identifier.wosid000308698600002-
dc.date.tcdate2019-01-01-
dc.citation.endPage2701-
dc.citation.number6-
dc.citation.startPage2687-
dc.citation.titleJOURNAL OF IMMUNOLOGY-
dc.citation.volume189-
dc.contributor.affiliatedAuthorLee, SW-
dc.identifier.scopusid2-s2.0-84866177483-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc20-
dc.type.docTypeArticle-
dc.subject.keywordPlusT-CELLS-
dc.subject.keywordPlusIMMUNE REGULATION-
dc.subject.keywordPlusVITAMIN-A-
dc.subject.keywordPlusACID-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordPlusRESPONSES-
dc.subject.keywordPlusMICROBIOTA-
dc.subject.keywordPlusINDUCTION-
dc.subject.keywordPlusSYSTEM-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaImmunology-

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이승우LEE, SEUNG WOO
Dept of Life Sciences
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