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Identification of Acvr2a as a Th17 Cell-Specific Gene Induced during Th17 Differentiation

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dc.contributor.authorIhn, Hyun-ju-
dc.contributor.authorKim, Dong Hyeok-
dc.contributor.authorOh, Sang-Seok-
dc.contributor.authorMoon, Chaerin-
dc.contributor.authorChung, Jin Woong-
dc.contributor.authorSong, Hyunkeun-
dc.contributor.authorKim, Kwang Dong-
dc.date.accessioned2022-12-27T02:52:20Z-
dc.date.available2022-12-27T02:52:20Z-
dc.date.issued2011-11-
dc.identifier.issn0916-8451-
dc.identifier.issn1347-6947-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/23500-
dc.description.abstractIL-17-producing T lymphocytes have been found to comprise a distinct lineage of T helper cells (Th17 cells) that are major causes of autoimmune diseases such as EAE, RA, and IBD. In this study, we found that activin receptor type-2A (Acvr2a) is a gene induced during the differentiation of this effector cell lineage as compared with naive T cells. The transcript of Acvr2a was not induced in Th1 and Th2 cells, and both TGF-beta and IL-6 were required for the induction of Acvr2a. When the differentiation of Th17 cells was inhibited by all tarans retinoic acid (ATRA) which induces regulatory T cell (Treg) differentiation under Th17 differentiation conditions, expression of Acvr2a was also inhibited. Hence we propose that Acvr2a is a Th17 specific gene making Th17 cells distinct from other helper T cells, Th1, Th2, and Treg.-
dc.format.extent4-
dc.language영어-
dc.language.isoENG-
dc.publisherTAYLOR & FRANCIS LTD-
dc.titleIdentification of Acvr2a as a Th17 Cell-Specific Gene Induced during Th17 Differentiation-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1271/bbb.110436-
dc.identifier.scopusid2-s2.0-82155181565-
dc.identifier.wosid000297610500010-
dc.identifier.bibliographicCitationBIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, v.75, no.11, pp 2138 - 2141-
dc.citation.titleBIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY-
dc.citation.volume75-
dc.citation.number11-
dc.citation.startPage2138-
dc.citation.endPage2141-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaFood Science & Technology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryChemistry, Applied-
dc.relation.journalWebOfScienceCategoryFood Science & Technology-
dc.subject.keywordPlusROR-GAMMA-T-
dc.subject.keywordPlusHELPER-CELLS-
dc.subject.keywordPlusINTERLEUKIN-17-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusPATHWAYS-
dc.subject.keywordPlusPROMOTES-
dc.subject.keywordPlusTRANSCRIPTION-
dc.subject.keywordPlusINFLAMMATION-
dc.subject.keywordPlusPOPULATION-
dc.subject.keywordPlusGENERATION-
dc.subject.keywordAuthorhelper type 17 T cell (Th17)-
dc.subject.keywordAuthorAcvr2a-
dc.subject.keywordAuthorTGF-beta-
dc.subject.keywordAuthorIL-6-
dc.subject.keywordAuthorall trans retinoic acid (ATRA)-
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