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Cited 187 time in webofscience Cited 190 time in scopus
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dc.contributor.authorKataru, RP-
dc.contributor.authorKim, H-
dc.contributor.authorJang, C-
dc.contributor.authorChoi, DK-
dc.contributor.authorKoh, BI-
dc.contributor.authorKim, M-
dc.contributor.authorGollamudi, S-
dc.contributor.authorKim, YK-
dc.contributor.authorLee, SH-
dc.contributor.authorKoh, GY-
dc.date.accessioned2016-03-31T09:09:38Z-
dc.date.available2016-03-31T09:09:38Z-
dc.date.created2011-05-18-
dc.date.issued2011-01-28-
dc.identifier.issn1074-7613-
dc.identifier.other2011-OAK-0000024969-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/16738-
dc.description.abstractLymph node lymphatic vessels (LNLVs) serve as a conduit to drain antigens from peripheral tissues to within the lymph nodes. LNLV density is known to be positively regulated by vascular endothelial growth factors secreted by B cells, macrophages, and dendritic cells (DCs). Here, we show that LNLV formation was negatively regulated by T cells. In both steady and inflammatory states, the density of LNLVs was increased in the absence of T cells but decreased when T cells were restored. Interferon-gamma secretion by T cells suppressed lymphatic-specific genes in lymphatic endothelial cells and consequently caused marked reduction in LNLV formation. When T cells were depleted, recruitment of antigen-carrying DCs to LNs was augmented, reflecting a compensatory mechanism for antigen presentation to T cells through increased LNLVs. Thus, T cells maintain the homeostatic balance of LNLV density through a negative paracrine action of interferon-gamma.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherCELL PRESS-
dc.relation.isPartOfIMMUNITY-
dc.titleT Lymphocytes Negatively Regulate Lymph Node Lymphatic Vessel Formation-
dc.typeArticle-
dc.contributor.college생명과학과-
dc.identifier.doi10.1016/J.IMMUNI.2010.12.016-
dc.author.googleKataru, RP-
dc.author.googleKim, H-
dc.author.googleJang, C-
dc.author.googleChoi, DK-
dc.author.googleKoh, BI-
dc.author.googleKim, M-
dc.author.googleGollamudi, S-
dc.author.googleKim, YK-
dc.author.googleLee, SH-
dc.author.googleKoh, GY-
dc.relation.volume34-
dc.relation.issue1-
dc.relation.startpage96-
dc.relation.lastpage107-
dc.contributor.id10103891-
dc.relation.journalIMMUNITY-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationIMMUNITY, v.34, no.1, pp.96 - 107-
dc.identifier.wosid000287336600013-
dc.date.tcdate2019-01-01-
dc.citation.endPage107-
dc.citation.number1-
dc.citation.startPage96-
dc.citation.titleIMMUNITY-
dc.citation.volume34-
dc.contributor.affiliatedAuthorKim, YK-
dc.contributor.affiliatedAuthorKoh, GY-
dc.identifier.scopusid2-s2.0-78751688024-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc113-
dc.description.scptc105*
dc.date.scptcdate2018-05-121*
dc.type.docTypeArticle-
dc.subject.keywordPlusIFN-GAMMA-
dc.subject.keywordPlusINTERFERON-GAMMA-
dc.subject.keywordPlusINDUCED LYMPHANGIOGENESIS-
dc.subject.keywordPlusANTIGEN PRESENTATION-
dc.subject.keywordPlusENDOTHELIAL-CELLS-
dc.subject.keywordPlusINFLAMMATION-
dc.subject.keywordPlusMECHANISMS-
dc.subject.keywordPlusSYSTEM-
dc.subject.keywordPlusVEGF-
dc.subject.keywordPlusVASCULATURE-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaImmunology-

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고규영KOH, GOU YOUNG
Div of Molecular & Life Science
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