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Interferon-gamma inhibits in vitro mobilization of eosinophils by interleukin-5

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dc.contributor.authorPark, Choon-Sik-
dc.contributor.authorChoi, Eun Nam-
dc.contributor.authorKim, Jung Sun-
dc.contributor.authorChoi, Yun Sung-
dc.contributor.authorRhim, Tai Youn-
dc.contributor.authorChang, Hun Soo-
dc.contributor.authorChung,Il Yup-
dc.date.accessioned2021-06-24T00:37:58Z-
dc.date.available2021-06-24T00:37:58Z-
dc.date.issued2005-03-
dc.identifier.issn1018-2438-
dc.identifier.issn1423-0097-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/46515-
dc.description.abstractBackground: Th2 cytokines play pivotal roles in allergic inflammation, including eosinophilia, and their actions are antagonized by Th1 cytokines, conferring them therapeutic potential. Methods: In this study, we examined the ability of a number of cytokines to suppress the activation of eosinophils that function as effector cells for allergic airway diseases. Results: Interleukin (IL)-5, IL-6, and tumor necrosis factor (TNF) induced an eosinophil shape change, whereas interferon (IFN)-gamma significantly inhibited the shape change. Other cytokines, including IL-1, IL-4, IL-10 and IL-13, had little or only slightly enhancing or reducing effects on the shape change. We further analyzed the IFN-gamma effect, showing that pretreatment with IFN-gamma strongly suppressed IL-5-induced eosinophil shape change, and cycloheximide (CHX) abrogated the suppression by IFN-gamma, suggesting that new protein synthesis is required for the inhibitory effect by this cytokine. In agreement with these results, IFN-gamma blocked the eosinophil migration and ERK phophorylation induced by IL-5, and the addition of CHX restored eosinophil chemotaxis. Conclusions: Collectively, IFN-gamma may attenuate eosinophilic inflammation by directly negating eosinophil mobilization. Copyright (C) 2005 S. Karger AG, Basel.-
dc.format.extent8-
dc.language영어-
dc.language.isoENG-
dc.publisherS. Karger AG-
dc.titleInterferon-gamma inhibits in vitro mobilization of eosinophils by interleukin-5-
dc.typeArticle-
dc.publisher.location스위스-
dc.identifier.doi10.1159/000083957-
dc.identifier.scopusid2-s2.0-17244376776-
dc.identifier.wosid000227694100011-
dc.identifier.bibliographicCitationInternational Archives of Allergy and Immunology, v.136, no.3, pp 295 - 302-
dc.citation.titleInternational Archives of Allergy and Immunology-
dc.citation.volume136-
dc.citation.number3-
dc.citation.startPage295-
dc.citation.endPage302-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaAllergy-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalWebOfScienceCategoryAllergy-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.subject.keywordPlusINDUCED AIRWAY HYPERRESPONSIVENESS-
dc.subject.keywordPlusIFN-GAMMA-
dc.subject.keywordPlusT-CELLS-
dc.subject.keywordPlusMESSENGER-RNA-
dc.subject.keywordPlusMICE-
dc.subject.keywordPlusINFLAMMATION-
dc.subject.keywordPlusASTHMA-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusRESPONSES-
dc.subject.keywordPlusRECEPTOR-
dc.subject.keywordAuthorasthma-
dc.subject.keywordAuthoreosinophils-
dc.subject.keywordAuthorinterferon-gamma-
dc.subject.keywordAuthorinterleukin-5-
dc.subject.keywordAuthorinterleukin-6-
dc.subject.keywordAuthortumor necrosis factor-
dc.identifier.urlhttps://www.karger.com/Article/FullText/83957-
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