Analysis on regulatory mechanism of B cell selection by novel signaling molecule in germinal center
Analysis on regulatory mechanism of B cell selection by novel signaling molecule in germinal center
批准号:
23590568
负责人:
HIKIDA Masaki
金额:
$3.33万
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:
2011
资助国家:
日本
项目状态:
已结题
起止时间:
2011 至 2013
中文摘要
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英文摘要
We have found that a subset of germinal center B cells is expressing CD3e, which have been widely known as a T cell-specific signaling molecule. The germinal center B cells we have observed were proliferating cells and we have also observed that CD3e is involved in apoptosis of these B cells. These results suggest that still unknown molecules are playing essential roles in positive and/or negative selection in the germinal center B cells. Also, we have found that this cell number of this population was increased in a autoimmune-prone model mice strain compared to the wild type mice. This may suggest the involvement of this population in autoimmune diseases.
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Roles of Igβ in the generation of autoreactive B cells in BXSB-Yaa autoimmune prone mice
Igβ 在 BXSB-Yaa 自身免疫倾向小鼠中自身反应性 B 细胞生成中的作用
DOI:
--
发表时间:
2013
期刊:
影响因子:
--
作者:
[Ikumi Katano, Ryoji Ito, Takeshi Takahashi, Mamoru Ito, Masaki Hikida]
通讯作者:
Masaki Hikida
Roles of Igβin the generation of autoreactive B cells in BXSB-Yaa autoimmune prone mouse
Igβ 在 BXSB-Yaa 自身免疫倾向小鼠自身反应性 B 细胞生成中的作用
DOI:
--
发表时间:
2012
期刊:
影响因子:
--
作者:
[瀬谷司, 松本美佐子, Todo Kagefumi and Masaki Hikida]
通讯作者:
Todo Kagefumi and Masaki Hikida
IgG1 cytoplasmic tail is essential for cell surface expression in Igβ down-regulated cells.
IgG1 胞质尾对于 Igβ 下调细胞的细胞表面表达至关重要。
DOI:
10.1016/j.bbrc.2014.02.037
发表时间:
2014
期刊:
Biochem.Biophys.Res.Commun.
影响因子:
--
作者:
[Kagefumi Todo, Orie Koga, Miwako Nishikawa, Masaki Hikida]
通讯作者:
Masaki Hikida
Roles of Igb in the generation of autoreactive B cells in BXSB-Yaa autoimmune prone mice
Igb 在 BXSB-Yaa 自身免疫倾向小鼠自身反应性 B 细胞生成中的作用
DOI:
--
发表时间:
2013
期刊:
影响因子:
--
作者:
[TakeshiTakahashi, Ikumi Katano, Ryoji Ito, Mamoru Ito, Masaki Hikida and Todo Kagefumi]
通讯作者:
Masaki Hikida and Todo Kagefumi
Analyses on novel selection and regulatory mechanisms of IgG-positive memory B cells
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批准号:19K07618
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资助金额:$2.75万
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财政年份:2019
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负责人:HIKIDA Masaki
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依托单位:
Analysis on the roles of PLCγ2 in generation and maintenance of immunological memory
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财政年份:2008
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负责人:HIKIDA Masaki
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Regulation of auto-reactive B cell activation by Ras signaling pathway
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财政年份:2006
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负责人:HIKIDA Masaki
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Roles of BCR signaling mediated by PLC-γ2 on memory response
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批准号:16590414
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.3万
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财政年份:2004
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负责人:HIKIDA Masaki
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依托单位:
Visualization of alteration of antigen specificity in mature B lymphocytes by multiple fluorescent labelling
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批准号:12650789
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$0.77万
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财政年份:2000
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负责人:HIKIDA Masaki
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依托单位:
海外基金