○種別 (必須): |
○言語 (必須): | □ | 英語
| [継承] |
○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) Erdenebayar Namjil (日) (読)
○役割 (任意): |
○貢献度 (任意): |
○学籍番号 (推奨): |
| [継承] |
| 2. | 前川 洋一
○役割 (任意): |
○貢献度 (任意): |
○学籍番号 (推奨): |
| [継承] |
| 3. | 西田 純
○役割 (任意): |
○貢献度 (任意): |
○学籍番号 (推奨): |
| [継承] |
| 4. | 北村 明子
○役割 (任意): |
○貢献度 (任意): |
○学籍番号 (推奨): |
| [継承] |
| 5. | 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] |
○題名 (必須): | □ | (英) Protein-tyrosine phosphatase-kappa regulates CD4+ T cell development through ERK1/2-mediated signaling. (日)
| [継承] |
○副題 (任意): |
○要約 (任意): | □ | (英) T cells express diverse antigen-specific receptors and are required for eradicating pathogens and transformed cells. T cells expressing CD4 acquire helper effector functions and those expressing CD8 exert cytotoxic activity after antigen recognition. The protein-tyrosine phosphatase, receptor type kappa (PTPRKappa) is mutated in LEC rats, resulting in impaired CD4(+) T cell development in the thymus. However, the molecular mechanism of PTPRK controlling CD4(+) T cell development remains unclear. We demonstrate herein that inhibition of PTPRK by transducing a dominant negative form of the intracellular domain of PTPRK (PTPRK-ICD-DN) in bone marrow-derived stem cells suppresses the development of CD4(+) T cells. The inhibition of PTPRK by PTPRK-ICD-DN or short-hairpin RNA for PTPRK attenuates ERK1/2 phosphorylation in T cells after PMA and ionomycin stimulation. Total thymocytes from LEC rats also showed weaker phosphorylation of ERK1/2 after PMA and ionomycin stimulation than control thymocytes. Furthermore, inhibition of PTPRK by PTPRK-ICD-DN suppressed MEK1/2 and c-Raf phosphorylation, which is required for ERK1/2 phosphorylation. These data indicate that PPTRK positively regulates ERK1/2 phosphorylation, which impacts CD4(+) T cell development. (日)
| [継承] |
○キーワード (推奨): | 1. | (英) Animals (日) (読)
| [継承] |
| 2. | (英) CD4-Positive T-Lymphocytes (日) (読)
| [継承] |
| 3. | (英) Humans (日) (読)
| [継承] |
| 4. | (英) Jurkat Cells (日) (読)
| [継承] |
| 5. | (英) MAP Kinase Kinase 1 (日) (読)
| [継承] |
| 6. | (英) MAP Kinase Kinase 2 (日) (読)
| [継承] |
| 7. | (英) Mice (日) (読)
| [継承] |
| 8. | (英) Mitogen-Activated Protein Kinase 1 (日) (読)
| [継承] |
| 9. | (英) Mitogen-Activated Protein Kinase 3 (日) (読)
| [継承] |
| 10. | リン酸化 (phosphorylation)
| [継承] |
| 11. | (英) Rats (日) (読)
| [継承] |
| 12. | (英) Receptor-Like Protein Tyrosine Phosphatases, Class 2 (日) (読)
| [継承] |
| 13. | シグナル伝達 (signal transduction)
| [継承] |
○発行所 (推奨): |
○誌名 (必須): | □ | Biochemical and Biophysical Research Communications ([Elsevier])
(pISSN: 0006-291X, eISSN: 1090-2104)
○ISSN (任意): | □ | 1090-2104
ISSN: 0006-291X
(pISSN: 0006-291X, eISSN: 1090-2104) Title: Biochemical and biophysical research communicationsTitle(ISO): Biochem Biophys Res CommunPublisher: Elsevier B.V. (NLM Catalog)
(Scopus)
(CrossRef)
(Scopus information is found. [need login])
| [継承] |
| [継承] |
○巻 (必須): | □ | 390
| [継承] |
○号 (必須): | □ | 3
| [継承] |
○頁 (必須): | □ | 489 493
| [継承] |
○都市 (任意): |
○年月日 (必須): | □ | 西暦 2009年 10月 1日 (平成 21年 10月 1日)
| [継承] |
○URL (任意): |
○DOI (任意): | □ | 10.1016/j.bbrc.2009.09.117 (→Scopusで検索)
| [継承] |
○PMID (任意): | □ | 19800317 (→Scopusで検索)
| [継承] |
○CRID (任意): |
○WOS (任意): |
○Scopus (任意): | □ | 2-s2.0-70449701442
| [継承] |
○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: Department of Immunology and Parasitology, Institute of Health Biosciences, The University of Tokushima Graduate School, Tokushima, Japan. (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] |