FUNCTIONAL CHARACTERIZATION OF CD69
FUNCTIONAL CHARACTERIZATION OF CD69
批准号:
6349869
负责人:
Steven F Ziegler
金额:
$31.82万
依托单位国家:
美国
项目类别:
财政年份:
1999
资助国家:
美国
项目状态:
已结题
起止时间:
1999-02-15 至 2004-01-31
关键词:
中文摘要
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION (Adapted from Investigator's Abstract): The, immune system
is regulated by specific cell-cell interactions that are mediated
through an elaborate array of cell-surface receptors. While the identity
of many of the cell-surface receptors is known, the mechanisms by which
they exert their influence on immune responses remains obscure in most
instances. This is especially true in autoimmune diseases, where the
failure to regulate immune responses properly results in a pathological
state. Among the cell surface receptors implicated in normal, as well
as inflammatory, responses, is CD69. CD69 is expressed on the surface
of activated, but not resting, cells of all hematopoietic lineages. It
has been shown to be involved in a wide variety of biological processes,
including the positive selection of thymocytes, induction of
proinflammatory cytokine release from monocytes, and T cell co-
stimulation. In spite of the overwhelming evidence demonstrating the
importance of CD69 to the development and function of the immune system,
there is very little known as to how CD69 is regulated or how it
functions. Very basic issues, such as the mechanism of CD69 signal
transduction and the nature of its cognate ligand, as well as more
global issues such as its role in mounting a competent immune response
and propagating a chronic pathological state, remain unanswered. A wide
body of evidence suggests that CD69 plays an important role in two
aspects of the immune system, thymocyte development and T cell
activation, that are also areas of immune dysfunction in autoimmune
disease. However, before an assessment of CD69's role in autoimmune
disease can be made, a detailed analysis of its role in the normal
development and function of the immune system must be performed. The
experiments described in this proposal will address basic questions
concerning the role of CD69 in the positive selection of thymocytes, as
well as the mechanism by which CD69 transmits intracellular signals. We
will also identify and characterize the cell surface molecule on
monocytes that serves as the CD69 receptor. Knowing this information
will allow a detailed analysis of the role of CD69 in the initiation and
propagation of autoimmune disease to be initiated.
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财政年份:2020
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Epithelial control of responses to allergen challenge and viral exacerbation
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资助金额:$167.83万
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Epithelial control of responses to allergen challenge and viral exacerbation
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资助金额:$159.11万
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IL-33 and food allergy
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批准号:9509328
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资助金额:$56.63万
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财政年份:2016
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负责人:Steven F Ziegler
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依托单位:
IL-33 and food allergy
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批准号:9304962
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资助金额:$70.95万
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依托单位:
A FOXP3 complex that controls human regulatory T cell function
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资助金额:$27.19万
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财政年份:2015
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依托单位:
A FOXP3 complex that controls human regulatory T cell function
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批准号:9052703
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资助金额:$42.45万
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财政年份:2015
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依托单位:
Control of tumor growth and metastasis by the cytokine TSLP
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资助金额:$9.47万
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资助金额:$42.75万
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财政年份:2014
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依托单位:
A FOXP3 complex that controls human regulatory T cell function
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资助金额:$43.7万
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财政年份:2014
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依托单位:
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财政年份:2014
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依托单位:
c-Ski and the regulation of CD4 T cell-mediated autoimmunity and tolerance
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资助金额:$42.75万
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财政年份:2014
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负责人:Steven F Ziegler
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依托单位:
Control of tumor growth and metastasis by the cytokine TSLP
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依托单位:
海外基金