○種別 (必須): | □ | 学術論文 (審査論文)
| [継承] |
○言語 (必須): | □ | 英語
| [継承] |
○招待 (推奨): |
○審査 (推奨): | □ | Peer Review
| [継承] |
○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. | 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): |
○貢献度 (任意): |
○学籍番号 (推奨): |
| [継承] |
| 2. | (英) Doyle C (日) (読)
○役割 (任意): |
○貢献度 (任意): |
○学籍番号 (推奨): |
| [継承] |
| 3. | (英) Miele L (日) (読)
○役割 (任意): |
○貢献度 (任意): |
○学籍番号 (推奨): |
| [継承] |
| 4. | (英) Fuchs C (日) (読)
○役割 (任意): |
○貢献度 (任意): |
○学籍番号 (推奨): |
| [継承] |
| 5. | (英) Germain RN (日) (読)
○役割 (任意): |
○貢献度 (任意): |
○学籍番号 (推奨): |
| [継承] |
○題名 (必須): | □ | (英) The duration of antigen receptor signalling determines CD4+ versus CD8+ T-cell lineage fate (日)
| [継承] |
○副題 (任意): |
○要約 (任意): | □ | (英) Signals elicited by binding of the T-cell antigen receptor and the CD4/CD8 co-receptor to major histocompatibility complex (MHC) molecules control the generation of CD4+ (helper) or CD8+ (cytotoxic) T cells from thymic precursors that initially express both co-receptor proteins. These precursors have unique, clonally distributed T-cell receptors with unpredictable specificity for the self-MHC molecules involved in this differentiation process. However, the mature T cells that emerge express only the CD4 (MHC class II-binding) or CD8 (MHC class I-binding) co-receptor that complements the MHC class-specificity of the T-cell receptor. How this matching of co-receptor-defined lineage and T-cell-receptor specificity is achieved remains unknown, as does whether signalling by the T-cell receptors, co-receptors and/or general cell-fate regulators such as Notch-1 contributes to initial lineage choice, to subsequent differentiation processes or to both. Here we show that the CD4 versus CD8 lineage fate of immature thymocytes is controlled by the co-receptor-influenced duration of initial T-cell receptor-dependent signalling. Notch-1 does not appear to be essential for this fate determination, but it is selectively required for CD8+ T-cell maturation after commitment directed by T-cell receptors. This indicates that the signals constraining CD4 versus CD8 lineage decisions are distinct from those that support subsequent differentiation events such as silencing of co-receptor loci. (日)
| [継承] |
○キーワード (推奨): | 1. | (英) Animals (日) (読)
| [継承] |
| 2. | (英) Antigens, CD (日) (読)
| [継承] |
| 3. | (英) Antigens, CD4 (日) (読)
| [継承] |
| 4. | (英) Antigens, CD8 (日) (読)
| [継承] |
| 5. | (英) Antigens, Differentiation, T-Lymphocyte (日) (読)
| [継承] |
| 6. | (英) CD4-Positive T-Lymphocytes (日) (読)
| [継承] |
| 7. | (英) CD8-Positive T-Lymphocytes (日) (読)
| [継承] |
| 8. | (英) Cell Lineage (日) (読)
| [継承] |
| 9. | (英) Cells, Cultured (日) (読)
| [継承] |
| 10. | (英) Female (日) (読)
| [継承] |
| 11. | (英) Lectins, C-Type (日) (読)
| [継承] |
| 12. | (英) Leukopoiesis (日) (読)
| [継承] |
| 13. | (英) Ligands (日) (読)
| [継承] |
| 14. | (英) Major Histocompatibility Complex (日) (読)
| [継承] |
| 15. | (英) Male (日) (読)
| [継承] |
| 16. | (英) Membrane Proteins (日) (読)
| [継承] |
| 17. | (英) Mice (日) (読)
| [継承] |
| 18. | (英) Mice, Inbred C57BL (日) (読)
| [継承] |
| 19. | (英) Mice, Transgenic (日) (読)
| [継承] |
| 20. | (英) Models, Immunological (日) (読)
| [継承] |
| 21. | (英) Receptor, Notch1 (日) (読)
| [継承] |
| 22. | (英) Receptors, Antigen, T-Cell (日) (読)
| [継承] |
| 23. | (英) Receptors, Cell Surface (日) (読)
| [継承] |
| 24. | (英) Signal Transduction (日) (読)
| [継承] |
| 25. | (英) Thymus Gland (日) (読)
| [継承] |
| 26. | (英) Time Factors (日) (読)
| [継承] |
| 27. | (英) Transcription Factors (日) (読)
| [継承] |
○発行所 (推奨): |
○誌名 (必須): | □ | Nature ([Nature Publishing Group])
(pISSN: 0028-0836, eISSN: 1476-4687)
○ISSN (任意): | □ | 0028-0836
ISSN: 0028-0836
(pISSN: 0028-0836, eISSN: 1476-4687) Title: NatureTitle(ISO): NaturePublisher: Nature Portfolio (NLM Catalog)
(Scopus)
(CrossRef)
(Scopus information is found. [need login])
| [継承] |
| [継承] |
○巻 (必須): | □ | 404
| [継承] |
○号 (必須): | □ | 6777
| [継承] |
○頁 (必須): | □ | 506 510
| [継承] |
○都市 (任意): |
○年月日 (必須): | □ | 西暦 2000年 3月 30日 (平成 12年 3月 30日)
| [継承] |
○URL (任意): |
○DOI (任意): | □ | 10.1038/35006664 (→Scopusで検索)
| [継承] |
○PMID (任意): | □ | 10761920 (→Scopusで検索)
| [継承] |
○CRID (任意): |
○WOS (任意): |
○Scopus (任意): |
○評価値 (任意): |
○被引用数 (任意): |
○指導教員 (推奨): |
○備考 (任意): | 1. | (英) Article.Affiliation: Lymphocyte Biology Section, Laboratory of Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA. (日)
| [継承] |
| 2. | (英) Article.PublicationTypeList.PublicationType: Journal Article (日)
| [継承] |
| 3. | (英) Article.PublicationTypeList.PublicationType: Research Support, Non-U.S. Gov't (日)
| [継承] |
| 4. | (英) Article.PublicationTypeList.PublicationType: Research Support, U.S. Gov't, P.H.S. (日)
| [継承] |