Regulation of the expression of immature thymocyte antigen-1 (IMT-1) during T-cell development in thymus

胸腺 T 细胞发育过程中未成熟胸腺细胞抗原 1 (IMT-1) 表达的调节

基本信息

  • 批准号:
    09670333
  • 负责人:
  • 金额:
    $ 1.98万
  • 依托单位:
  • 依托单位国家:
    日本
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
  • 财政年份:
    1997
  • 资助国家:
    日本
  • 起止时间:
    1997 至 1998
  • 项目状态:
    已结题

项目摘要

Previously. we produced a monoclonal antibody that recognizes immature thymocyte antigen-1 (IMT- 1). IMT- 1 is expressed on thymocytes from the late differentiation stage of CD4^-CD8^- to that of CD4^+CD8^+. When CD4^+CD8^+ thymocytes differentiate into CD^++8^+ or CD4^-8^+ cells, IMT-1 disappears from the cell surface (Kishi et aL, J.Immunol. . 155 : 568-577, 1995). In this study. we Investigated the regulation of IMT- 1 expression by TCR signaling. When the expression of IMT- 1 on thymocytes in T-cell-receptor (TCR) transgenic mice was analyzed, IMT- 1 expression was found to be decreased on thymocytes that received signals inducing positive or negative selection. Furthermore, IMT- 1 expression on CD4^+CD8^+ thymocytes was reduced, when thyrnocytes were stimulated by anti-CD3 antibody. These results Indicate that IMT- 1 expression on CD4^+CD8^+ thymocytes is regulated by signals through alphabetaTCR (Kishi et aL, Int. Immunol., 10 : 951-960, 1998). Then we examined the effect of pre-TCR on the expression of IMT- 1 . It was observed that pre-TCR and IMT- 1 is coordinately expressed on fetal thymocytes durIng fetal thymocyte development and that pre-TCR and IMT- 1 were downregulated by the stimulation of RAG2^-/^- thymocytes with anti-CD3 antibody with corresponding kinetics (Tong et aL, Immunol., 96 : 48-56, 1999). These data demonstrate that during T-cell development in thymus, LMT-1 expression Is regulated by the signals through pre-TCR as well as TCR and indicate the involvement of IMT-1 in T-cell development.
之前。我们生产了一种识别未成熟胸腺细胞抗原-1 (IMT- 1)的单克隆抗体。IMT- 1在胸腺细胞上的表达从CD4^-CD8^-分化后期到CD4^+CD8^+分化后期。当CD4^+CD8^+胸腺细胞分化为CD^++8^+或CD4^-8^+细胞时,IMT-1从细胞表面消失(Kishi et aL, J.Immunol.)。[j]。在这项研究中。我们研究了TCR信号对IMT- 1表达的调控。分析t细胞受体(T-cell-receptor, TCR)转基因小鼠胸腺细胞上IMT- 1的表达,发现在接受阳性或阴性选择信号的胸腺细胞上IMT- 1的表达降低。此外,当抗cd3抗体刺激甲状腺细胞时,CD4^+CD8^+胸腺细胞上的IMT- 1表达降低。这些结果表明IMT- 1在CD4^+CD8^+胸腺细胞上的表达是通过alphabetaTCR信号调节的(Kishi et aL, Int.)。Immunol。[j] .农业科学,1998(10):951-960。然后我们检测了预tcr对IMT- 1表达的影响。研究发现,在胎儿胸腺细胞发育过程中,pre-TCR和IMT- 1在胎儿胸腺细胞上协调表达,并且anti-CD3抗体刺激RAG2^-/^-胸腺细胞具有相应的动力学,从而下调pre-TCR和IMT- 1 (Tong et aL, immuno1)。农业学报,96:48-56,1999)。这些数据表明,在胸腺t细胞发育过程中,IMT-1的表达受到TCR前和TCR信号的调控,表明IMT-1参与了t细胞的发育。

项目成果

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Hiroyuki Kishi: "A murine monoclonal antibody(928)recognizing a new epitope formed with a combination of HLA-DPA1 0201 and DPB1 0301 gene products" Human Immunology. 56. 114-124 (1997)
Hiroyuki Kishi:“一种鼠单克隆抗体(928),可识别由 HLA-DPA1 0201 和 DPB1 0301 基因产物组合形成的新表位”《人类免疫学》。
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    0
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Tong,J.-J.et al.: "Coordinate expression of pre-T cell receptor complex and as novel immature thymocyte-specific antigen,IMT-1,during thymocyte development" Immunology. 96. 48-56 (1999)
Tong, J.-J. 等人:“胸腺细胞发育过程中前 T 细胞受体复合物的协调表达和新型未成熟胸腺细胞特异性抗原 IMT-1”免疫学。
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    0
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Kishi, H.et al.: "Immature thymocyte antigen-1 : A novel thymocyte marker discriminating pre-and post selected thymocytes" International Immunology. 10. 951-960 (1998)
Kishi, H.等人:“未成熟胸腺细胞抗原-1:一种新型胸腺细胞标记,可区分选择前和选择后的胸腺细胞”国际免疫学。
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    0
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Tong, J.J, et al.: "Coordinate expression of pre-T cell receptor complex and a novel immature thymocyte-specific antigen, IMT-1, during thymocyte development" Immunology. 96. 48-56 (1999)
Tong, J.J, 等人:“胸腺细胞发育过程中前 T 细胞受体复合物和新型未成熟胸腺细胞特异性抗原 IMT-1 的协调表达”免疫学。
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    0
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Hiroyuki Kishi: "Immature thymocyte antigen-1:A novel thymocyte marker discriminating pre-and post-selected thymocytes" International Immunology. (in press). (1998)
Hiroyuki Kishi:“未成熟胸腺细胞抗原-1:一种新型胸腺细胞标记,可区分选择前和选择后的胸腺细胞”国际免疫学。
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KISHI Hiroyuki其他文献

TCR repertoire analysis of peptide-specific T cells using immunospot array assay on a chip (T-ISAAC) technology
使用芯片上免疫点阵列测定 (T-ISAAC) 技术对肽特异性 T 细胞进行 TCR 谱分析
  • DOI:
  • 发表时间:
    2018
  • 期刊:
  • 影响因子:
    0
  • 作者:
    KOBAYASHI Eiji;MURAGUCHI Atsushi;KISHI Hiroyuki
  • 通讯作者:
    KISHI Hiroyuki
Development of a novel tumor antigen-specific TCR cloning system using a microarray chip
使用微阵列芯片开发新型肿瘤抗原特异性 TCR 克隆系统
  • DOI:
  • 发表时间:
    2020
  • 期刊:
  • 影响因子:
    0
  • 作者:
    KOBAYASHI Eiji;OZAWA Tatsuhiko;HAMANA hiroshi;MURAGUCHI Atsushi;KISHI Hiroyuki
  • 通讯作者:
    KISHI Hiroyuki
A rapid and easy system providing cDNAs cloning of antigen specific TCRs from single human and mouse T-cells within 4 days
一种快速、简单的系统,可在 4 天内从单个人类和小鼠 T 细胞中克隆抗原特异性 TCR 的 cDNA
  • DOI:
  • 发表时间:
    2016
  • 期刊:
  • 影响因子:
    0
  • 作者:
    HAMANA Hiroshi;KISHI Hiroyuki;SHITAOKA Kiyomi;OZAWA Tatsuhiko;MURAGUCHI Atsushi
  • 通讯作者:
    MURAGUCHI Atsushi
Establishment of West Nile virus - neutralizing human monoclonal antibodies derived from the individuals vaccinated with inactivated Japanese encephalitis virus by ISAAC technology (2nd.)
通过ISAAC技术建立西尼罗河病毒-中和来自接种灭活日本脑炎病毒的个体的人单克隆抗体(第二次)
  • DOI:
  • 发表时间:
    2015
  • 期刊:
  • 影响因子:
    0
  • 作者:
    MASAKI Hideyuki;OZAWA Tatsuhiko;TAKASAKI Tomohiko;KISHI Hiroyuki;MURAGUCHI Atsushi
  • 通讯作者:
    MURAGUCHI Atsushi

KISHI Hiroyuki的其他文献

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{{ truncateString('KISHI Hiroyuki', 18)}}的其他基金

Preparation of CCP antibodies library in Rheumatoid Arthritis and its clinical application
类风湿性关节炎CCP抗体库的制备及其临床应用
  • 批准号:
    20591167
  • 财政年份:
    2008
  • 资助金额:
    $ 1.98万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Development of the method for detection of antigen-specific lymphocytes and antigen receptors using cell-microarray
开发利用细胞微阵列检测抗原特异性淋巴细胞和抗原受体的方法
  • 批准号:
    15390176
  • 财政年份:
    2003
  • 资助金额:
    $ 1.98万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Apoptosis signals in autoimmune disease
自身免疫性疾病中的细胞凋亡信号
  • 批准号:
    13670453
  • 财政年份:
    2001
  • 资助金额:
    $ 1.98万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
A role of T cell receptor beta on immature thymoctye differentiation
T细胞受体β对未成熟胸腺细胞分化的作用
  • 批准号:
    05670304
  • 财政年份:
    1993
  • 资助金额:
    $ 1.98万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (C)
The structure and function of beta TCR on immature thymocytes.
β TCR 对未成熟胸腺细胞的结构和功能。
  • 批准号:
    03807028
  • 财政年份:
    1991
  • 资助金额:
    $ 1.98万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (C)

相似海外基金

Analysis of the expression and function of T cell differentiation antigen-CD7
T细胞分化抗原CD7的表达及功能分析
  • 批准号:
    08670376
  • 财政年份:
    1996
  • 资助金额:
    $ 1.98万
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    Grant-in-Aid for Scientific Research (C)
Analysis of the expression and function of T cell differentiation antigen-CD7
T细胞分化抗原CD7的表达及功能分析
  • 批准号:
    05670312
  • 财政年份:
    1993
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    $ 1.98万
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    Grant-in-Aid for General Scientific Research (C)
GENE ENCODING P67 MYELOID DIFFERENTIATION ANTIGEN
编码 P67 骨髓分化抗原的基因
  • 批准号:
    3079476
  • 财政年份:
    1988
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    $ 1.98万
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GENE ENCODING P67 MYELOID DIFFERENTIATION ANTIGEN
编码 P67 骨髓分化抗原的基因
  • 批准号:
    3079477
  • 财政年份:
    1988
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    $ 1.98万
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LEU 2/T8 CELL DIFFERENTIATION ANTIGEN GENE
LEU 2/T8 细胞分化抗原基因
  • 批准号:
    2900608
  • 财政年份:
    1986
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    $ 1.98万
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LEU-2/TS T CELL DIFFERENTIATION ANTIGEN GENE
LEU-2/TS T 细胞分化抗原基因
  • 批准号:
    3287031
  • 财政年份:
    1986
  • 资助金额:
    $ 1.98万
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LEU-2 T/8 T CELL DIFFERENTIATION ANTIGEN GENE
LEU-2 T/8 T 细胞分化抗原基因
  • 批准号:
    3287032
  • 财政年份:
    1986
  • 资助金额:
    $ 1.98万
  • 项目类别:
LEU 2/T8 CELL DIFFERENTIATION ANTIGEN GENE
LEU 2/T8 细胞分化抗原基因
  • 批准号:
    2684799
  • 财政年份:
    1986
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    $ 1.98万
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THE LEU-2/T8 T CELL DIFFERENTIATION ANTIGEN GENE
LEU-2/T8 T 细胞分化抗原基因
  • 批准号:
    3287029
  • 财政年份:
    1986
  • 资助金额:
    $ 1.98万
  • 项目类别:
LEU 2 T/8 T CELL DIFFERENTIATION ANTIGEN GENE
LEU 2 T/8 T 细胞分化抗原基因
  • 批准号:
    2177689
  • 财政年份:
    1986
  • 资助金额:
    $ 1.98万
  • 项目类别:
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