Protein Phosphatases in Lymphocyte Signal Transduction
Protein Phosphatases in Lymphocyte Signal Transduction
批准号:
7408064
负责人:
Tse-Hua Tan
金额:
$34.88万
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-07-01 至 2010-03-31
关键词:
AblationAntibody FormationApoptosisAutoimmunityBiochemical GeneticsCell Cycle ProgressionCell Cycle RegulationCell ProliferationCell Proliferation RegulationCell physiologyCellsCentrosomeCollagen ArthritisDiseaseEvaluationExperimental ArthritisExperimental Autoimmune EncephalomyelitisFutureGene TargetingGenetic RecombinationImmune System DiseasesImmune responseImmunizationInfectionInflammatory ResponseInkIntegration Host FactorsKnock-outKnockout MiceLeadLymphocyteMAPK8 geneMediatingModelingMusNF-kappa BOkadaic AcidPathway interactionsPhosphoric Monoester HydrolasesPhysiologicalProtein Phosphatase 2A Regulatory Subunit PR53Protein Serine/Threonine PhosphataseProtein phosphataseRetroviridaeRoleSignal PathwaySignal TransductionStructure of germinal center of lymph nodeSystemT-Cell ActivationT-Cell DevelopmentT-Cell ProliferationT-LymphocyteTestingTh1/Th2 Differentiation PathwayTherapeutic AgentsTransgenic Micebasecell mediated immune responsedesignembryonic stem cellin vivoleukemia/lymphomamouse modelnovel
中文摘要
描述(由申请人提供):INK和NF-kappaB参与t细胞活化/分化、炎症反应、细胞凋亡和细胞增殖。蛋白磷酸酶4 (PP4)是一种冈田酸敏感蛋白丝氨酸/苏氨酸磷酸酶。迄今为止,人们对PP4的功能知之甚少。我们的研究结果为PP4/JNK和PP4/ NF-kappaB模块的存在提供了第一个证据,作为控制T细胞信号通路的新范例。了解PP4介导的t细胞信号转导的潜在机制将有助于发现PP4的功能。本申请计划研究PP4在t细胞信号传导和t细胞介导的免疫应答中的作用。为了揭示PP4在T细胞中的新生理功能,我们将使用Cre-foxP重组系统和Lck-Cre转基因小鼠产生PP4敲除细胞和小鼠。这些方法包括:(1)利用各种生化和遗传学方法了解PP4在t细胞增殖、凋亡、分化、中心体功能和信号传导中的作用;(2)研究PP4在体内Th1/Th2分化、免疫反应和自身免疫中的功能。最后,我们计划剖析免疫应答、白血病/淋巴瘤和免疫性疾病中pp4介导的各种信号通路。我们未来对参与pp4介导的淋巴细胞信号通路的宿主因子的理解,将为发现、设计和评估有效的细胞内治疗白血病/淋巴瘤、感染和免疫疾病(如自身免疫)的药物提供基础信息。具体目标是:目标1。利用PP4条件敲除小鼠和细胞研究PP4在t细胞增殖、凋亡、分化和信号转导中的作用。目标2。利用t细胞特异性PP4条件敲除小鼠研究PP4在t细胞介导的免疫反应和自身免疫中的体内功能。
英文摘要
DESCRIPTION (provided by applicant): INK and NF-kappaB are involved in T-cell activation/differentiation, inflammatory responses, apoptosis, and cell proliferation. Protein phosphatase 4 (PP4) is an okadaic acid-sensitive protein serine/threonine phosphatase. To date, little is known about the functions of PP4. Our results provide the first evidence for the existence of PP4/JNK and PP4/ NF-kappaB modules as a new paradigm for the control of the signaling pathways in T cells. Understanding the underlying mechanisms of PP4-mediated T-cell signal transduction will lead to the discovery of the functions of PP4. This application plans to study the roles of PP4 in T-cell signaling and T-cell mediated immune responses. To unveil novel physiological functions of PP4 in T cells, we will generate PP4 knockout cells and mice using the Cre-foxP recombination system and Lck-Cre transgenic mice. The approaches are: (i) to understand the roles PP4 in T-cell proliferation, apoptosis, differentiation, centrosome function, and signaling using various biochemical and genetic approaches, and (ii) to study the in vivo functions of PP4 in Th1/Th2 differentiation, immune responses, and autoirnmunity. Ultimately, we plan to dissect various PP4-mediated signaling pathways in immune responses, leukemia/lymphoma, and immunological diseases. Our future understanding of host factors involved in the PP4-mediated lymphocyte signaling pathways will provide information fundamental to the discovery, design, and evaluation of effective intracellular therapeutic agents for leukemia/lymphoma, infections, and immunological disorders such as autoimmunity. The specific aims are: Aim 1. Study the roles of PP4 in T-cell proliferation, apoptosis, differentiation, and signaling using PP4 conditional knockout mice and cells. Aim 2. Study in vivo functions of PP4 in T-cell mediated immune responses and autoimmunity using Tcell specific PP4 conditional knockout mice.
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Protein Phosphatases in Lymphocyte Signal Transduction
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批准号:6964971
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项目类别:
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资助金额:$31.88万
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财政年份:2005
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负责人:Tse-Hua Tan
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依托单位:
Protein Phosphatases in Lymphocyte Signal Transduction
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批准号:7082143
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项目类别:
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资助金额:$36.62万
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财政年份:2005
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负责人:Tse-Hua Tan
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依托单位:
PP4 and IGF-1 Signaling in Breast Tumorigenesis
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批准号:6864953
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项目类别:
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资助金额:$12.9万
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财政年份:2005
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负责人:Tse-Hua Tan
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依托单位:
Protein Phosphatases in Lymphocyte Signal Transduction
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批准号:7614172
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项目类别:
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资助金额:$34.88万
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财政年份:2005
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负责人:Tse-Hua Tan
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依托单位:
Protein Phosphatases in Lymphocyte Signal Transduction
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批准号:7204167
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项目类别:
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资助金额:$35.56万
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财政年份:2005
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负责人:Tse-Hua Tan
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依托单位:
PP4 and IGF-1 Signaling in Breast Tumorigenesis
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批准号:7054698
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项目类别:
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资助金额:$12.6万
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财政年份:2005
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负责人:Tse-Hua Tan
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依托单位:
Protein Phosphatases and Proinflammatory Cytokines
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批准号:7046096
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项目类别:
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资助金额:$26.16万
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财政年份:2002
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负责人:Tse-Hua Tan
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依托单位:
Protein Phosphatases and Proinflammatory Cytokines
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批准号:6891095
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项目类别:
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资助金额:$26.79万
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财政年份:2002
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负责人:Tse-Hua Tan
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依托单位:
Protein Phosphatases and Proinflammatory Cytokines
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批准号:6485662
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项目类别:
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资助金额:$26.79万
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财政年份:2002
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负责人:Tse-Hua Tan
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依托单位:
Protein Phosphatases and Proinflammatory Cytokines
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批准号:6732605
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项目类别:
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资助金额:$26.79万
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财政年份:2002
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负责人:Tse-Hua Tan
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依托单位:
Protein Phosphatases and Proinflammatory Cytokines
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批准号:6626056
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项目类别:
-
资助金额:$26.79万
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财政年份:2002
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负责人:Tse-Hua Tan
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依托单位:
HPK1-Mediated Lymphocyte Signal Transduction Mechanisms
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批准号:7023516
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项目类别:
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资助金额:$30.0万
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财政年份:1998
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负责人:Tse-Hua Tan
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依托单位:
HPK1 MEDIATED T CELL SIGNAL TRANSDUCTION MECHANISMS
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批准号:2714924
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项目类别:
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资助金额:$21.09万
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财政年份:1998
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负责人:Tse-Hua Tan
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依托单位:
HPK1 MEDIATED T CELL SIGNAL TRANSDUCTION MECHANISMS
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批准号:6373782
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项目类别:
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资助金额:$53.67万
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财政年份:1998
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负责人:Tse-Hua Tan
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依托单位:
HPK1 MEDIATED T CELL SIGNAL TRANSDUCTION MECHANISMS
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批准号:2887678
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项目类别:
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资助金额:$21.76万
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财政年份:1998
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负责人:Tse-Hua Tan
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依托单位:
HPK1 MEDIATED T CELL SIGNAL TRANSDUCTION MECHANISMS
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批准号:6170765
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项目类别:
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资助金额:$22.6万
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财政年份:1998
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负责人:Tse-Hua Tan
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依托单位:
HPK1 MEDIATED T CELL SIGNAL TRANSDUCTION MECHANISMS
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批准号:6534098
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项目类别:
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资助金额:$23.98万
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财政年份:1998
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负责人:Tse-Hua Tan
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依托单位:
Molecular and Cellular Mechanisms of Host Defense
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批准号:6917304
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项目类别:
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资助金额:$25.94万
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财政年份:1996
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负责人:Tse-Hua Tan
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依托单位:
Molecular and Cellular Mechanisms of Host Defense
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批准号:8080279
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项目类别:
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资助金额:$19.0万
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财政年份:1996
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负责人:Tse-Hua Tan
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依托单位:
Molecular and Cellular Mechanisms of Host Defense
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批准号:7858164
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项目类别:
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资助金额:$21.28万
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财政年份:1996
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负责人:Tse-Hua Tan
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依托单位:
海外基金