Lymphocyte Activation and Signaling
淋巴细胞激活和信号转导
基本信息
- 批准号:7058629
- 负责人:
- 金额:$ 0.75万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2006
- 资助国家:美国
- 起止时间:2006-01-01 至 2006-12-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
The cells of the immune system are armed with a dizzying array of signaling receptors requiring them to integrate an enormous amount of information about their environment to mount the appropriate biologic response. Over the last several years much has been learned about the biochemical nature of the signaling cascades initiated by interactions of individual receptors with their ligands. This progress presents an exciting new challenge, namely, to understand how multiple signals are integrated in the context of the entire cell to bring about the ultimate cellular response. We propose to bring together distinguished scientists working at the cutting edge of immune cell signaling to describe their new findings and to address how these issues relate to human disease. The proposed meeting will provide a view of how the initial encounter of
immune cell signaling receptor with their ligands ultimately leads to the biological response be it activation, differentiation, movement, or cell death and how this knowledge is being translated to important clinical problems in autoimmunity, immunodeficiency, vaccines, tumor immunity, transplantation and infectious diseases. The organizers of this conference have designed a program that will bring together principal investigators, fellows and students who are exploring how signaling pathways are integrated within and among immune cells to yield the appropriate response and how these signaling pathways may be manipulated to alter immune cell function for therapeutic purposes.
免疫系统的细胞武装着令人眼花dry乱的信号受体,要求它们整合有关其环境的大量信息以安装适当的生物反应。在过去的几年中,关于通过单个受体与配体的相互作用引发的信号传导级联反应的生化性质。这一进步提出了一个令人兴奋的新挑战,即了解如何在整个细胞的背景下集成多个信号,以引起最终的细胞响应。我们建议将在免疫细胞信号传导的最前沿工作的杰出科学家汇集在一起,以描述其新发现,并解决这些问题与人类疾病的关系。拟议的会议将提供有关如何初次相遇的观点
具有配体的免疫细胞信号受体最终导致生物学反应,包括激活,分化,运动或细胞死亡,以及如何将这些知识转化为自身免疫性,免疫缺陷,疫苗,肿瘤免疫,移植和感染疾病的重要临床问题。该会议的组织者设计了一项计划,该计划将汇集主要研究人员,研究员和学生,他们正在探索信号传导途径如何在内部和免疫细胞内部整合,以产生适当的反应以及如何操纵这些信号传导途径以改变免疫细胞功能以实现治疗目的。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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GARY A. KORETZKY其他文献
GARY A. KORETZKY的其他文献
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{{ truncateString('GARY A. KORETZKY', 18)}}的其他基金
Regulation of T Cell and Mast Cell Function by DGKzeta
DGKzeta 对 T 细胞和肥大细胞功能的调节
- 批准号:
8093168 - 财政年份:2010
- 资助金额:
$ 0.75万 - 项目类别:
Regulation of Integrin Signaling by Adapter Proteins
接头蛋白对整合素信号传导的调节
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7323902 - 财政年份:2007
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$ 0.75万 - 项目类别:
SIGNAL TRANSDUCTION IN THE IMMUNE SYSTEM-FASEB CONF.
免疫系统中的信号转导 - FASEB CONF。
- 批准号:
6940539 - 财政年份:2005
- 资助金额:
$ 0.75万 - 项目类别:
2005 Immunochemistry and Immunobiology Gordon Conference
2005年免疫化学和免疫生物学戈登会议
- 批准号:
6993506 - 财政年份:2005
- 资助金额:
$ 0.75万 - 项目类别:
Regulation of T Cell and Mast Cell Function by DGKzeta
DGKzeta 对 T 细胞和肥大细胞功能的调节
- 批准号:
7342494 - 财政年份:2004
- 资助金额:
$ 0.75万 - 项目类别:
Regulation of T Cell and Mast Cell Function by DGKzeta
DGKzeta 对 T 细胞和肥大细胞功能的调节
- 批准号:
7009321 - 财政年份:2004
- 资助金额:
$ 0.75万 - 项目类别:
Regulation of PMN activation by SLP-76, PRAM-1 and ADAP
SLP-76、PRAM-1 和 ADAP 对 PMN 激活的调节
- 批准号:
7225954 - 财政年份:2004
- 资助金额:
$ 0.75万 - 项目类别:
Regulation of T Cell and Mast Cell Function by DGKzeta
DGKzeta 对 T 细胞和肥大细胞功能的调节
- 批准号:
7172927 - 财政年份:2004
- 资助金额:
$ 0.75万 - 项目类别:
Regulation of T Cell and Mast Cell Function by DGKzeta
DGKzeta 对 T 细胞和肥大细胞功能的调节
- 批准号:
6845716 - 财政年份:2004
- 资助金额:
$ 0.75万 - 项目类别:
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