The role of Cdc42 and Rac in NK cell activation
The role of Cdc42 and Rac in NK cell activation
批准号:
7314116
负责人:
CHRISTOPH WUELFING
金额:
$19.63万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-09-15 至 2009-08-31
关键词:
Activated Natural Killer CellAddressBiosensorCancer cell lineCell LineCell Surface ReceptorsCell physiologyCell surfaceCellsCouplesCytolysisDataElementsFoundationsFutureGuanosine Triphosphate PhosphohydrolasesImmune systemInterferonsInvestigationLeadLifeMaintenanceMalignant NeoplasmsMolecular AnalysisMonitorNK Cell ActivationNatural Killer CellsPathway interactionsPatternPhysiologicalPlayPositioning AttributeProteinsReagentRegulationRoleSignal PathwaySignal TransductionSuggestionT-LymphocyteTestingWiskott-Aldrich Syndromebasecancer therapycell killingcell typeimprovedinsightinterestkillingsneoplastic cellreceptorresearch studyrho GTP-Binding Proteinsspatiotemporaltumor
中文摘要
描述(由申请人提供):自然杀伤(NK)细胞是免疫系统的中枢效应细胞。它们在形成紧密的NK细胞/靶细胞对后杀死病毒感染和肿瘤靶细胞。有效的杀伤需要NK细胞朝向细胞界面移动。NK细胞极化的调节仍然知之甚少。密切相关的Rho GTP酶Cdc 42和Rac是许多细胞类型中细胞极化的中心调节因子。Cdc 42和Rac的激活剂Vav和Cdc 42的直接效应物Wiskott-Aldrich综合征蛋白(WASP)是有效杀伤NK细胞所必需的。在IL-2培养的NK细胞系中,Rac是杀伤所需的。然而,Cdc 42在一般情况下和Rac在原代NK细胞中的作用尚不清楚。作为本申请的重点,我们将阐明这些作用。我们完全有能力这样做。多年来,我们一直在研究原代细胞中NK细胞的极化和活化。研究Cdc 42在原代T细胞,我们已经产生了多种试剂Cdc 42/Rac活性和活细胞生物传感器的操作,以确定其活性的亚细胞定位。在初步数据中,Cdc 42和Rac活性的操纵影响NK细胞杀伤,支持它们在初级NK细胞活化中的重要性。此外,Cdc 42和Rac在原代NK细胞/肿瘤细胞对中以重叠但不同的模式被激活。由于定位对于活细胞中的功能至关重要,这些模式可以指导Cdc 42和Rac的作用的有效调查。在第一个目标中,将评估NK细胞表面受体对Cdc 42和Rac的激活,重点是NKG 2D。许多受体可以激活NK细胞。NKG 2D特别令人感兴趣,似乎与已知在其他细胞类型中激活Cdc 42/Rac的信号传导途径偶联,并且因为它在抗癌NK活性中作为活化受体发挥主要生理作用。在第二个目标中,由Cdc 42/Rac调节的T细胞极化和活化的元件将通过短期和定量地操纵Cdc 42/Rac活性来鉴定。总之,这些实验将表征Cdc 42/Rac激活,并确定由Cdc 42/Rac调节的NK细胞功能的各个方面,重点是NKG 2D。除了对Cdc 42/Rac功能的直接洞察之外,这些数据将为未来更全面地分析原代NK细胞中Rho GTPases的分子途径奠定基础。此外,由于NK细胞极化对于NK杀伤肿瘤细胞至关重要且限制NK杀伤肿瘤细胞,因此我们的研究有望建立合理的方法来增强NK细胞极化,以在治疗上促进抗肿瘤NK活性,我们将在未来进行测试。自然杀伤细胞是免疫系统的中心效应器,其杀死病毒感染细胞和肿瘤细胞。在这里,他们的激活的调节将被研究。对NK细胞功能调节的更好理解可以预期导致改进的疗法,特别是在癌症治疗中。
英文摘要
DESCRIPTION (provided by applicant): Natural killer (NK) cells are central effectors of the immune system. They kill virally infected and tumor target cells following formation of tight NK cell/target cell couples. Effective killing requires NK cells to polarize towards the cellular interface. The regulation of NK cell polarization is still poorly understood. The closely related Rho GTPases Cdc42 and Rac are central regulators of cellular polarization in numerous cell types. An activator of Cdc42 and Rac, Vav, and an immediate effector of Cdc42, Wiskott-Aldrich Syndrome protein (WASP), are required for effective NK cell killing. Rac is required for killing in IL-2-cultured NK cell lines. However, roles of Cdc42 in general and of Rac in primary NK cells are less clear. As the focus of this application, we will elucidate such roles. We are well positioned to do so. We have studied NK cell polarization and activation in primary cells for years. Studying Cdc42 in primary T cells, we have generated multiple reagents for the manipulation of Cdc42/Rac activity and live cell biosensors to determine the sub-cellular localization of their activity. In preliminary data, manipulation of Cdc42 and Rac activity impacted NK cell killing, supporting their importance in primary NK cell activation. In addition, Cdc42 and Rac were activated in primary NK cell/tumor cell couples in overlapping yet distinct patterns. As localization is critical for function in live cells, these patterns can guide an efficient investigation of roles of Cdc42 and Rac. In the first aim, activation of Cdc42 and Rac by NK cell surface receptors will be assessed with an emphasis on NKG2D. Numerous receptors can active NK cells. NKG2D is of particular interest, as if couples to signaling pathways known to active Cdc42/Rac in other cell types, and as it plays a major physiological role as an activating receptor in anti-cancer NK activity. In the second aim, elements of T cell polarization and activation that are regulated by Cdc42/Rac will be identified by manipulating Cdc42/Rac activity short-term and quantitatively. Together these experiments will characterize Cdc42/Rac activation and identify aspects of NK cell function that are regulated by Cdc42/Rac with an emphasis on NKG2D. Beyond the immediate insight into Cdc42/Rac function, these data will generate the foundation for a future, more comprehensive analysis of the molecular pathways governing Rho GTPases in primary NK cells. Moreover, as NK cell polarization is critical for and limiting in NK killing of tumor cells, our studies can be expected to establish rational means to enhance NK cell polarization to promote anti-tumor NK activity therapeutically, as we will test in the future. Natural killer cells are central effectors of the immune system that kill virally infected and tumor cells. Here the regulation of their activation will be studied. An improved understanding of the regulation of NK cell function can be expected to lead to improved therapies, in particular in the treatment of cancers.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
A quantative understanding of the regulation of actin dynamics in live T cells
-
批准号:7727778
-
项目类别:
-
资助金额:$19.63万
-
财政年份:2009
-
负责人:CHRISTOPH WUELFING
-
依托单位:
A quantative understanding of the regulation of actin dynamics in live T cells
-
批准号:7876792
-
项目类别:
-
资助金额:$19.63万
-
财政年份:2009
-
负责人:CHRISTOPH WUELFING
-
依托单位:
The role of Cdc42 and Rac in NK cell activation
-
批准号:7496602
-
项目类别:
-
资助金额:$19.25万
-
财政年份:2007
-
负责人:CHRISTOPH WUELFING
-
依托单位:
The Function of the immunological synapse
-
批准号:6910870
-
项目类别:
-
资助金额:$7.8万
-
财政年份:2004
-
负责人:CHRISTOPH WUELFING
-
依托单位:
The Function of the immunological synapse
-
批准号:6814700
-
项目类别:
-
资助金额:$7.8万
-
财政年份:2004
-
负责人:CHRISTOPH WUELFING
-
依托单位:
Regulation of the T Cell Cytoskeleton by Costimulation
-
批准号:6864481
-
项目类别:
-
资助金额:$27.77万
-
财政年份:2003
-
负责人:CHRISTOPH WUELFING
-
依托单位:
Regulation of the T Cell Cytoskeleton by Costimulation
-
批准号:7185771
-
项目类别:
-
资助金额:$26.33万
-
财政年份:2003
-
负责人:CHRISTOPH WUELFING
-
依托单位:
Regulation of the T Cell Cytoskeleton by Costimulation
-
批准号:7822094
-
项目类别:
-
资助金额:$1.1万
-
财政年份:2003
-
负责人:CHRISTOPH WUELFING
-
依托单位:
Regulation of the T Cell Cytoskeleton by Costimulation
-
批准号:7025088
-
项目类别:
-
资助金额:$27.12万
-
财政年份:2003
-
负责人:CHRISTOPH WUELFING
-
依托单位:
Regulation of the T Cell Cytoskeleton by Costimulation
-
批准号:6729973
-
项目类别:
-
资助金额:$27.77万
-
财政年份:2003
-
负责人:CHRISTOPH WUELFING
-
依托单位:
Regulation of the T Cell Cytoskeleton by Costimulation
-
批准号:6579666
-
项目类别:
-
资助金额:$27.77万
-
财政年份:2003
-
负责人:CHRISTOPH WUELFING
-
依托单位:
海外基金