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。
基本信息
- 批准号:03807028
- 负责人:
- 金额:$ 1.15万
- 依托单位:
- 依托单位国家:日本
- 项目类别:Grant-in-Aid for General Scientific Research (C)
- 财政年份:1991
- 资助国家:日本
- 起止时间:1991 至 1992
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Recently it has been shown that the expression of betaTCR is an important step in the differentiation of CD4^-8^- thymocytes into CD4^+8^+ cells ant that the betaTCR chain is expressed on immature thymocytes in the absence of other TCR chains.In order to study the structure of the immature betaTCR complex and its function in thymocyte differentiation,a thymic lymphoma cell line (LSB11-1)was established.LSB11-1 cells express betaTCR on the cell surface but few CD3.Also in this cell line,betaTCR is not associated with alphaTCR.alphaTCR-gene-transfectant of LSB11-1 cells,LSB11-1alpha29, express alphabetaTCR with CD3 complex on the cell surface.Recently it has been shown that IgD molecules could be expressed on the cell surface in the absence of mbl molecules which correspond to CD3 in B cells,and that those IgD molecules are linked with glycosylphosphatidylinositol(GPI). Treatment of LSB11-1 cells with phosphatidylinositol specific phospholipase C(PI-PLC)reduced the expression of betaTCR on LSB11-1 cells,indicating that the betaTCR is GPI-linked,although the expression of alphabetaTCR on LSB11-1alpha29 cells was not changed by PI-PLC treatment.Cell surface expression of GPI-linked betaTCR was also found on CD3^-,betaTCR^+ thymocytes in betaTCR transgenic mice.However CD3^<high>,betaTCR^<high> mature thymocytes did not express GPI-linked betaTCR on the cell surface,indicating that immature thymocytes can express the GPI-linked betaTCR.Although a transient increase in cytoplasmic CA^<2+> was observed when LSB11-1alpha29 cells were stimulated with betaTCR antibodies or CD3 antibodies,cytoplasmic CA^<2+> increase in LSB11-1 cells was not found when stimulated with those antibodies.Presently we are investigating what kind of signal is transduced via the immature betaTCR complex.These results should show the role of immature betaTCR complex in differentiation of immature thymocytes.
为了研究未成熟胸腺细胞βTCR复合体的结构及其在胸腺细胞分化中的作用,建立了胸腺淋巴瘤细胞系(LSB11-1)。该细胞表面表达βTCR,但CD3很少。在该细胞系中,βTCR与αTCR无关。近年来的研究表明,在B细胞中,在缺乏与CD3相对应的MBL分子的情况下,可以在细胞表面表达IGD分子,并且这些IGD分子与糖基磷脂酰肌醇(GPI)相连。用磷脂酰肌醇特异性磷脂酶C(PI-PLC)处理LSB11-1细胞,降低了LSB11-1细胞表面βTCR的表达,表明βTCR是GPI连接的,而未成熟的胸腺细胞表面GPI连接的βTCR的表达没有改变。在CD3^-、BetaTCR^+胸腺细胞表面也发现了GPI连接的BetaTCR的表达。然而,CD3;高、高、高成熟胸腺细胞表面不表达GPI连接的BetaTCR。当LSB11-1Alpha29细胞被βTCR抗体或CD3抗体刺激时,LSB11-1细胞中出现2+和gt;,而在这些抗体刺激下,LSB11-1细胞胞浆中的CA^<;2+和gt;没有增加。目前,我们正在研究未成熟的BetaTCR复合体通过什么样的信号转导。这些结果应该表明未成熟的BetaTCR复合体在未成熟胸腺细胞分化中的作用。
项目成果
期刊论文数量(18)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Borgulya,P.,Kishi,H.,Uematsu,Y.and von Boehmer,H: "Exclusion and inclusion of alpha and beta T cell receptor alleles" Cell. 69. 529-537 (1992)
Borgulya,P.、Kishi,H.、Uematsu,Y. 和 von Boehmer,H:“α 和 β T 细胞受体等位基因的排除和包含”细胞。
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- 影响因子:0
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Borgulya,P.,Kishi,H.,Mueller,U.,Kirberg,J.von Boehmer,H.: "Development of the CD4 and CD8 lineage of T cells;instruction versus selection." EMBO J.10. 913-918 (1991)
Borgulya,P.、Kishi,H.、Mueller,U.、Kirberg,J.von Boehmer,H.:“T 细胞 CD4 和 CD8 谱系的发育;指导与选择。”
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- 影响因子:0
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Kishi,H.,Borgulya,P.,Scott,B.,Karjalainen,K.,Traunecker,A.,Kaufman,J.and von Boehmer,H: "Surface expression of the beta T cell receptor(TCR)chain in the absence of other TCR or CD3 proteins on immature T cells" EMBO J. 10. 93-100 (1991)
Kishi,H.、Borgulya,P.、Scott,B.、Karjalainen,K.、Traunecker,A.、Kaufman,J. 和 von Boehmer,H:“β T 细胞受体 (TCR) 链的表面表达
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- 影响因子:0
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Kishi,H.,Borgulya,P.,Scott,B.,Karjalainen,K.,Traunecker,A.,von Boehmer,H.: "Surface expression of the T cell receptor(TCR)chain in the absence of other TCR or CD3 proteins on immature T cells." EMBO J.10. 93-100 (1991)
Kishi,H.、Borgulya,P.、Scott,B.、Karjalainen,K.、Traunecker,A.、von Boehmer,H.:“在没有其他 TCR 或
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- 影响因子:0
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Borgulya,P.,Kishi,H.,Uematsu,Y.,von Boehmer,H.: "Exclusion and inclusion of and T cell receptor alleles." Cell. 69. 529-537 (1992)
Borgulya,P.、Kishi,H.、Uematsu,Y.、von Boehmer,H.:“T 细胞受体等位基因的排除和包含。”
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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:
$ 1.15万 - 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:
$ 1.15万 - 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:
$ 1.15万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
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
- 批准号:
09670333 - 财政年份:1997
- 资助金额:
$ 1.15万 - 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:
$ 1.15万 - 项目类别:
Grant-in-Aid for General Scientific Research (C)
相似海外基金
GROWTH AND DIFFERENTIATION OF IMMATURE THYMOCYTES
未成熟胸腺细胞的生长和分化
- 批准号:
3030076 - 财政年份:1991
- 资助金额:
$ 1.15万 - 项目类别:
GROWTH AND DIFFERENTIATION OF IMMATURE THYMOCYTES
未成熟胸腺细胞的生长和分化
- 批准号:
3030075 - 财政年份:1991
- 资助金额:
$ 1.15万 - 项目类别:
A study on the mechanism of interaction of bone marrow-derived immature thymocytes with thymic dendritic cells
骨髓源性未成熟胸腺细胞与胸腺树突状细胞相互作用机制的研究
- 批准号:
03680140 - 财政年份:1991
- 资助金额:
$ 1.15万 - 项目类别:
Grant-in-Aid for General Scientific Research (C)
GROWTH AND DIFFERENTIATION OF IMMATURE THYMOCYTES
未成熟胸腺细胞的生长和分化
- 批准号:
3030077 - 财政年份:1991
- 资助金额:
$ 1.15万 - 项目类别:














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