Study on B cell differentiation signaling by using a novel system
Study on B cell differentiation signaling by using a novel system
批准号:
10470091
负责人:
KARASUYAMA Hajime
金额:
$8.45万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B).
财政年份:
1998
资助国家:
日本
项目状态:
已结题
起止时间:
1998 至 2000
中文摘要
前B细胞受体(preBCR)在B细胞发育的早期瞬时表达,在B细胞分化中起重要作用。前BCR传递何种信号诱导B细胞分化仍有待确定。在这项研究中,我们研究了前BCR信号转导通路,通过使用一个新的系统,我们最初开发的。我们纯化并测序了一个36 kD的蛋白质(pp 36),这是酪氨酸磷酸化的前BCR信号。相应的cDNA克隆显示,pp 36是一种新的蛋白质与脂质修饰的N-末端区域。由于已知这种脂质修饰对于蛋白质锚入脂筏是必不可少的,因此pp 36似乎在信号转导中起重要作用。
英文摘要
Pre B cell receptor (preBCR) is expressed transiently at the early stage of B cell development and plays an important role in B cell differentiation. It remains to be determined what kind of signals are delivered from preBCR to induce B cell differentiation. In this study, we examined the preBCR signal transduction pathway by using a novel system which we have originally developed. We purified and sequenced a 36 kD protein (pp36) that was tyrosine-phosphorylated by preBCR signaling. The cloning of a corresponding cDNA revealed that pp36 is a novel protein with lipid modification at the N-terminal region. Since this lipid modification is know to be essential for proteins to anchor into lipid raft, pp36 appears to play an important role in signal transduction.
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Nomura, K., Kanegane, H., Karasuyama, H., Tsukada, S., Agematsu, K., Murakami, G., Sakazume, S., Sako, M., Tanaka, R., Kuniya, Y., Komeno, T., Ishihara, S., Hayashi, K., Kishimoto, T.and Miyawaki, T.: "Genetic defect in human X-linked agammaglobulinemia i
野村,K.,兼金,H.,乌山,H.,冢田,S.,上松,K.,村上,G.,坂津,S.,佐子,M.,田中,R.,Kuniya,Y.,
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通讯作者:
Ohnishi, K., Shimizu, T., Karasuyama, H.and Melchers, F.: "The identification of a non-classical cadherin expressed during B cell development and its interaction with surrogate light chain."J.Biol.Chem.. 275. 31134-44 (2000)
Ohnishi, K.、Shimizu, T.、Karasuyama, H. 和 Melchers, F.:“B 细胞发育过程中表达的非经典钙粘蛋白的鉴定及其与替代轻链的相互作用。”J.Biol.Chem..
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烏山一: "B細胞初期分化とプレB細胞レセプターの発現"医学のあゆみ. 188. 202-203 (1999)
Kazuyama Karasuyama:“早期 B 细胞分化和前 B 细胞受体的表达”医学史 188. 202-203 (1999)。
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Kuramochi,S.: "Molecular cloning of the human gene STK10 encoding lymphocyte-oriented kinase and comparative chromosomal mapping of the human,mouse and rat homologues." Immunogenetics.
Kuramochi,S.:“编码淋巴细胞导向激酶的人类基因 STK10 的分子克隆以及人类、小鼠和大鼠同源物的比较染色体作图。”
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永田喜三郎: "Annual Review免疫 1999" 中外医学社, 1-13 (1998)
永田喜三郎:《免疫学年度评论 1999》《中外医学社》,1-13 (1998)
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共 38 条
Study on dynamics and function of basophils by using intravital imaging
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批准号:24390093
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$12.06万
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财政年份:2012
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负责人:KARASUYAMA Hajime
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依托单位:
Study on roles of basophils under physiological and pathological conditions
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批准号:21390116
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资助金额:$11.98万
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财政年份:2009
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负责人:KARASUYAMA Hajime
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依托单位:
Developmental regulation and dysregulation of immunological self
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批准号:19059007
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项目类别:Grant-in-Aid for Scientific Research on Priority Areas
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资助金额:$32.26万
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财政年份:2007
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负责人:KARASUYAMA Hajime
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依托单位:
Study on in vivo roles of basophils
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批准号:19390110
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$12.15万
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财政年份:2007
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负责人:KARASUYAMA Hajime
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依托单位:
Study on a novel mechanism by which IgE/FcεRI mediates chronic allergic inflammation
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批准号:16616004
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.43万
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财政年份:2004
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负责人:KARASUYAMA Hajime
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依托单位:
Dynamism of B cell development
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批准号:14370110
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$7.23万
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财政年份:2002
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负责人:KARASUYAMA Hajime
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依托单位:
Molecular mechanism of B cell development governed by surrogate light chain.
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批准号:08457110
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$4.48万
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财政年份:1996
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负责人:KARASUYAMA Hajime
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依托单位:
海外基金