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PLD1 activation mediates Amb a 1-induced Th2-associated cytokine expression via the JNK/ATF-2 pathway in BEAS-2B cells

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dc.contributor.authorKim, Joo-Hwa-
dc.contributor.authorChoi, Hye-Jin-
dc.contributor.authorOh, Cheong-Hae-
dc.contributor.authorOh, Jae-Won-
dc.contributor.authorHan, Joong-Soo-
dc.date.accessioned2022-07-15T20:26:18Z-
dc.date.available2022-07-15T20:26:18Z-
dc.date.created2021-05-11-
dc.date.issued2015-11-
dc.identifier.issn0008-8749-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/156039-
dc.description.abstractThe purpose of this study was to identify the role of phospholipase D1 (PLD1) in Amb a 1-induced IL-5 and IL-13 expression. When BEAS-2B cells were stimulated with Amb a 1, PLD activity increased, and knockdown of PLD1 decreased Amb a 1-induced IL-5 and IL-13 expression. Amb a 1 also activated the PLC gamma/p70S6K/JNK pathway. Furthermore, Amb a 1-induced PLD activation was also attenuated by PLC gamma inhibition, and knockdown of PLD1 decreased Amb a 1-induced activation of P70S6K and JNK. When ATF-2 activity was blocked with ATF-2 siRNA, Amb a 1-induced IL-5 and IL-13 expression was completely abolished, indicating that ATF-2 is a transcriptional factor required for the expression of IL-5 and IL-13 in response to Amb a 1. Taken together, we suggest that PLD1 acts as an important regulator in Amb a 1-induced expression of IL-5 and IL-13 via a PLC gamma/p70S6K/JNK/ATF-2 pathway in BEAS-2B cells.-
dc.language영어-
dc.language.isoen-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.titlePLD1 activation mediates Amb a 1-induced Th2-associated cytokine expression via the JNK/ATF-2 pathway in BEAS-2B cells-
dc.typeArticle-
dc.contributor.affiliatedAuthorOh, Jae-Won-
dc.contributor.affiliatedAuthorHan, Joong-Soo-
dc.identifier.doi10.1016/j.cellimm.2015.08.003-
dc.identifier.scopusid2-s2.0-84958541513-
dc.identifier.wosid000369168400002-
dc.identifier.bibliographicCitationCELLULAR IMMUNOLOGY, v.298, no.1-2, pp.9 - 17-
dc.relation.isPartOfCELLULAR IMMUNOLOGY-
dc.citation.titleCELLULAR IMMUNOLOGY-
dc.citation.volume298-
dc.citation.number1-2-
dc.citation.startPage9-
dc.citation.endPage17-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.subject.keywordPlusNITRIC-OXIDE SYNTHESIS-
dc.subject.keywordPlusPROTEIN-KINASE-C-
dc.subject.keywordPlusP70 S6 KINASE-
dc.subject.keywordPlusPHOSPHOLIPASE-D-
dc.subject.keywordPlusSIGNAL-TRANSDUCTION-
dc.subject.keywordPlusKAPPA-B-
dc.subject.keywordPlusRAGWEED-
dc.subject.keywordPlusRECEPTOR-
dc.subject.keywordPlusMTOR-
dc.subject.keywordPlusPHOSPHORYLATION-
dc.subject.keywordAuthorAmbrosia artemisiifolia-
dc.subject.keywordAuthorPLD1-
dc.subject.keywordAuthorJNK-
dc.subject.keywordAuthorp70S6K-
dc.subject.keywordAuthorIL-13-
dc.subject.keywordAuthorIL-5-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0008874915300095?via%3Dihub-
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서울 의과대학 > 서울 생화학·분자생물학교실 > 1. Journal Articles
서울 의과대학 > 서울 소아청소년과학교실 > 1. Journal Articles

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