『徳島大学 教育・研究者情報データベース (EDB)』---[学外] /
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EID=211765EID:211765, Map:0, LastModified:2024年3月29日(金) 15:36:03, Operator:[三木 ちひろ], Avail:TRUE, Censor:0, Owner:[安友 康二], Read:継承, Write:継承, Delete:継承.
種別 (必須):
言語 (必須): 英語 [継承]
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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)
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[継承]
2.前川 洋一
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学籍番号 (推奨):
[継承]
3.西田 純
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[継承]
4.北村 明子
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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])
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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 communications
Title(ISO): Biochem Biophys Res Commun
Publisher: Elsevier B.V.
 (NLM Catalog  (Scopus  (CrossRef (Scopus information is found. [need login])
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(必須): 390 [継承]
(必須): 3 [継承]
(必須): 489 493 [継承]
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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]
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Scopus (任意): 2-s2.0-70449701442 [継承]
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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]

標準的な表示

和文冊子 ● (種別) : Namjil Erdenebayar, Yoichi Maekawa, Jun Nishida, Akiko Kitamura and Koji Yasutomo : Protein-tyrosine phosphatase-kappa regulates CD4+ T cell development through ERK1/2-mediated signaling., Biochemical and Biophysical Research Communications, Vol.390, No.3, 489-493, (発行所), (都市), Oct. 2009.
欧文冊子 ● (種別) : Namjil Erdenebayar, Yoichi Maekawa, Jun Nishida, Akiko Kitamura and Koji Yasutomo : Protein-tyrosine phosphatase-kappa regulates CD4+ T cell development through ERK1/2-mediated signaling., Biochemical and Biophysical Research Communications, Vol.390, No.3, 489-493, (発行所), (都市), Oct. 2009.

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