○種別 (必須): | □ | 学術論文 (審査論文)
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○言語 (必須): | □ | 英語
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○招待 (推奨): |
○審査 (推奨): |
○カテゴリ (推奨): |
○共著種別 (推奨): |
○学究種別 (推奨): |
○組織 (推奨): |
○著者 (必須): | 1. | (英) Xu Mingli (日) (読)
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| 2. | (英) Morishima Noriko (日) (読)
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| 3. | (英) Mizoguchi Izuru (日) (読)
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| 4. | (英) Chiba Yukino (日) (読)
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| 5. | (英) Fujita Koji (日) (読)
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| 6. | (英) Kuroda Masahiko (日) (読)
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| 7. | (英) Iwakura Yoichiro (日) (読)
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| 8. | (英) Cua Daniel J (日) (読)
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| 9. | 安友 康二 ([徳島大学.大学院医歯薬学研究部.医学域.医科学部門.病理系.生体防御医学])
○役割 (任意): |
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| 10. | (英) Mizuguchi Junichiro (日) (読)
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| 11. | (英) Yoshimoto Takayuki (日) (読)
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○題名 (必須): | □ | (英) Regulation of the development of acute hepatitis by IL-23 through IL-22 and IL-17 production. (日)
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○副題 (任意): |
○要約 (任意): | □ | (英) IL-23 plays a critical role in the expansion of highly proinflammatory Th17 cells secreting IL-17 and IL-22. Recently, we demonstrated that Notch signaling drives IL-22 secretion through the aryl hydrocarbon receptor (AHR) and plays a protective role in Con A-induced hepatitis. In this study, we investigated the role of IL-23 in hepatitis using IL-23p19- and IL-17-deficient mice. In WT mice, the injection of Con A induced the upregulation of various cytokines which included IL-23, IL-22, IL-17, IFN- and TNF-. In IL-23p19-deficient mice, exacerbated hepatitis was observed and serum IL-22 and IL-17 levels were greatly reduced, whereas in IL-17-deficient mice, ameliorated hepatitis was observed. The injection of exogenous IL-22 protected p19-deficient mice from hepatitis, whereas the injection of exogenous IL-23 significantly increased the serum levels of not only IL-22 but also IL-17, and less effectively protected against hepatitis in IL-17-dependent and -independent manners. Finally, it was revealed that STAT3, STAT4 and Notch contributed to the production of both cytokines, and that the AHR was important only for IL-22 production in response to Con A and IL-23 in liver mononuclear cells. These results suggest that IL-23 plays a protective role in hepatitis through IL-22 production and also a pathological role via IL-17-dependent and -independent mechanisms. (日)
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○キーワード (推奨): | 1. | (英) Animals (日) (読)
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| 2. | (英) Concanavalin A (日) (読)
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| 3. | (英) Cytokines (日) (読)
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| 4. | (英) Hepatitis, Animal (日) (読)
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| 5. | (英) Interleukin-17 (日) (読)
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| 6. | (英) Interleukin-23 (日) (読)
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| 7. | (英) Interleukin-23 Subunit p19 (日) (読)
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| 8. | (英) Interleukins (日) (読)
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| 9. | (英) Mice (日) (読)
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| 10. | (英) Mice, Inbred C57BL (日) (読)
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| 11. | ノックアウトマウス (knockout mice)
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| 12. | (英) Receptors, Aryl Hydrocarbon (日) (読)
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| 13. | (英) Receptors, Notch (日) (読)
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| 14. | (英) Reverse Transcriptase Polymerase Chain Reaction (日) (読)
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| 15. | (英) STAT3 Transcription Factor (日) (読)
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| 16. | (英) STAT4 Transcription Factor (日) (読)
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| 17. | シグナル伝達 (signal transduction)
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| 18. | (英) Th17 Cells (日) (読)
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○発行所 (推奨): |
○誌名 (必須): | □ | European Journal of Immunology (European Federation of Immunological Societies)
(pISSN: 0014-2980, eISSN: 1521-4141)
○ISSN (任意): | □ | 1521-4141
ISSN: 0014-2980
(pISSN: 0014-2980, eISSN: 1521-4141) Title: European journal of immunologyTitle(ISO): Eur J ImmunolSupplier: European Federation of Immunological SocietiesPublisher: Wiley (NLM Catalog)
(Wiley)
(Scopus)
(CrossRef)
(Scopus information is found. [need login])
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○巻 (必須): | □ | 41
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○号 (必須): | □ | 10
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○頁 (必須): | □ | 2828 2839
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○都市 (任意): |
○年月日 (必須): | □ | 西暦 2011年 7月 18日 (平成 23年 7月 18日)
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○URL (任意): |
○DOI (任意): | □ | 10.1002/eji.201141291 (→Scopusで検索)
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○PMID (任意): | □ | 21953641 (→Scopusで検索)
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○CRID (任意): |
○WOS (任意): | □ | 000296199000006
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○備考 (任意): | 1. | (英) (日) 著者5.参照不要 確認済み
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| 2. | (英) Article.ELocationID: 10.1002/eji.201141291 (日)
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| 3. | (英) Article.Affiliation: Department of Immunoregulation, Institute of Medical Science, Tokyo Medical University, Shinjuku-ku, Tokyo, Japan. (日)
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| 4. | (英) Article.PublicationTypeList.PublicationType: Journal Article (日)
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| 5. | (英) Article.PublicationTypeList.PublicationType: Research Support, Non-U.S. Gov't (日)
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