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Cutting Edge: Progesterone Directly Upregulates Vitamin D Receptor Gene Expression for Efficient Regulation of T Cells by Calcitriol

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dc.contributor.authorThangamani, Shankar-
dc.contributor.authorKim, Myughoo-
dc.contributor.authorSon, Youngmin-
dc.contributor.authorHuang, Xinxin-
dc.contributor.authorKim, Heejoo-
dc.contributor.authorLee, Jee H.-
dc.contributor.authorCho, Jungyoon-
dc.contributor.authorUlrich, Benjamin-
dc.contributor.authorBroxmeyer, Hal E.-
dc.contributor.authorKim, Chang H.-
dc.date.accessioned2024-02-19T02:30:35Z-
dc.date.available2024-02-19T02:30:35Z-
dc.date.issued2015-02-
dc.identifier.issn0022-1767-
dc.identifier.issn1550-6606-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/72110-
dc.description.abstractThe two nuclear hormone receptor ligands progesterone and vitamin D (vit.D) play important roles in regulating T cells. The mechanism that connects these two hormones in regulating T cells has not been established. In this study, we report that progesterone is a novel inducer of vit.D receptor (VDR) in T cells and makes T cells highly sensitive to calcitriol. At the molecular level, the induction by progesterone is mediated by two progesterone receptor-binding elements in the intron region after the first noncoding exon of the human VDR gene. Increased expression of VDR by progesterone allows highly sensitive regulation of T cells by vit.D even when vit.D levels are suboptimal. This novel regulatory pathway allows enhanced induction of regulatory T cells but suppression of Th1 and Th17 cells by the two nuclear hormones. The results have significant ramifications in effective regulation of T cells to prevent adverse immune responses during pregnancy.-
dc.format.extent4-
dc.language영어-
dc.language.isoENG-
dc.publisherAMER ASSOC IMMUNOLOGISTS-
dc.titleCutting Edge: Progesterone Directly Upregulates Vitamin D Receptor Gene Expression for Efficient Regulation of T Cells by Calcitriol-
dc.typeArticle-
dc.identifier.doi10.4049/jimmunol.1401923-
dc.identifier.bibliographicCitationJOURNAL OF IMMUNOLOGY, v.194, no.3, pp 883 - 886-
dc.description.isOpenAccessN-
dc.identifier.wosid000348134000008-
dc.identifier.scopusid2-s2.0-84921494821-
dc.citation.endPage886-
dc.citation.number3-
dc.citation.startPage883-
dc.citation.titleJOURNAL OF IMMUNOLOGY-
dc.citation.volume194-
dc.type.docTypeArticle-
dc.publisher.location미국-
dc.subject.keywordPlusDENDRITIC CELLS-
dc.subject.keywordPlusPROMOTES-
dc.subject.keywordPlusD-3-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordPlusSUPPRESSES-
dc.subject.keywordPlusMODULATION-
dc.subject.keywordPlusPREGNANCY-
dc.subject.keywordPlusEXPANSION-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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생명공학대학 (시스템생명공학과)
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