Functional Role of Zebrafish TLR Proteins
Functional Role of Zebrafish TLR Proteins
批准号:
7527180
负责人:
CAROL H. KIM
金额:
$28.07万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-08-01 至 2013-05-31
关键词:
AffectAmoeba genusAntibioticsAntiviral AgentsBiological AssayBiological ModelsCommunicable DiseasesConditionDevelopmentDiseaseDisease ResistanceEatingEnvironmentEukaryotaEukaryotic CellEventHealthHumanHybridsImmuneImmune responseImmune systemIn VitroInfectionInterferon ActivationInterferon Type IInterventionInvestigationLeadLigand BindingLigandsLinkMammalsMediatingMethodsMutationNatural ImmunityOligonucleotidesOrganismPathway interactionsPlayProtein Binding DomainProteinsPublic HealthReceptor SignalingResistanceRoleSignal PathwaySignaling ProteinSwimmingSystemTNF geneTNF receptor-associated factor 2TNF receptor-associated factor 6TRAF2 geneTRAF6 geneTestingToll-Like Receptor PathwayToll-like receptorsVaccinesVertebratesViralVirusYeastsZebrafishdayfightinghuman TLR3 proteinimmune functionin vivoloss of functionmicrobialmutantnovelpathogenreceptorresearch studyresponseyeast two hybrid system
中文摘要
描述(申请人提供):我们假设斑马鱼TLR信号在机制上与哺乳动物不同,并预测了解这些差异将导致在高等脊椎动物中发现新的TLR信号通路。这项研究的一个关键焦点涉及免疫系统本身,特别是它的功能可以被增强、延伸和延长的方式。这些研究将确立哺乳动物TLR通路的起源,并最终为人类健康的新研究靶点和新疗法的发展提供方向。在这个提议中,我们打算实现以下特定目标:1.发现新的斑马鱼TLR信号通路组件a.鉴定识别病毒配体的斑马鱼TLR受体b.通过酵母双杂交筛选鉴定斑马鱼TLR通路的新相互作用因子c.确定在斑马鱼中发现的相互作用是否也发生在人类TLR通路中。这些实验将揭示斑马鱼TLR通路的新成分,并将为人类和斑马鱼的研究提供新的靶点。此外,还将阐明斑马鱼TLR蛋白相互作用的关键结构域。2.确定斑马鱼抗病毒途径组分在体内保护宿主免受感染中的作用TLR途径与抗病能力之间的联系是至关重要的。在体内的方法中,斑马鱼插入突变和吗啉寡核苷酸(MO)将被用来敲除TLR途径蛋白的表达。然后将丧失功能的突变体或变异体(注射吗啉的斑马鱼)暴露在病原体中,并进行检查,以确定先天免疫功能的变化如何影响对病原体挑战的抵抗力。
公共卫生相关性传染病继续在世界范围内的人类状况中发挥重要作用,因此,疫苗、抗生素和干预策略正在不断发展。这些方法在很大程度上被证明是有效的;然而,由于微生物的适应和环境引发的新疾病的出现,研究控制传染病的替代方法至关重要。这项研究的一个关键焦点涉及免疫系统本身,特别是它的功能可以被增强、延伸和延长的方式。
英文摘要
DESCRIPTION (provided by applicant): We hypothesize that zebrafish TLR signaling is mechanistically divergent from mammals, and predict that understanding these differences will lead to the discovery of novel TLR pathways in higher vertebrates. A critical focus of this investigation involves the immune system itself, specifically ways in which its function can be augmented, extended, and prolonged. These studies will establish the origins of the mammalian TLR pathways and ultimately provide a direction for development of new targets of investigation and new therapies for human health. In this proposal, we intend to fulfill the following SPECIFIC AIMS: 1. Discover novel zebrafish TLR signaling pathway components a. Identify the zebrafish TLR receptors that recognize viral ligands b. Identify novel interactors of the zebrafish TLR pathways via a yeast two-hybrid screen c. Determine if the interactions identified in the zebrafish also occur in the human TLR pathways These experiments will reveal new components of the zebrafish TLR pathways and will provide new targets for investigation in both human and zebrafish studies. Furthermore, the critical domains for protein-protein interaction of zebrafish TLR proteins will be elucidated. 2. Determine the role of the zebrafish antiviral pathway components in protecting the host from infection in vivo It is essential to demonstrate the link between TLR pathways and resistance to disease. In an in vivo approach, zebrafish insertional mutations and morpholino oligonucleotides (MO) will be used to knockdown the expression of the TLR pathway proteins. The loss-of-function mutants or morphants (morpholino-injected zebrafish) will then be exposed to pathogens and examined to determine how alterations in innate immune function affect resistance to pathogen challenge.
PUBLIC HEALTH RELEVANCE Infectious diseases continue to play a major role in the human condition worldwide and as a result vaccines, antibiotics, and intervention strategies are continually being developed. These methods have largely proven effective; however, due to microbial adaptation and environment- triggered emergence of new diseases, it is critical to investigate alternative methods for controlling infectious diseases. A critical focus of this investigation involves the immune system itself, specifically ways in which its function can be augmented, extended, and prolonged.
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Functional Role of Zebrafish TLR Proteins
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批准号:7939046
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项目类别:
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资助金额:$9.99万
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财政年份:2009
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负责人:CAROL H. KIM
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依托单位:
TLR Signaling Pathways in the Zebrafish
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批准号:7456858
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项目类别:
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资助金额:$22.28万
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财政年份:2008
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负责人:CAROL H. KIM
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依托单位:
Functional Role of Zebrafish TLR Proteins
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批准号:8274765
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项目类别:
-
资助金额:$27.49万
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财政年份:2008
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负责人:CAROL H. KIM
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依托单位:
Functional Role of Zebrafish TLR Proteins
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批准号:7666665
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项目类别:
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资助金额:$28.05万
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财政年份:2008
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负责人:CAROL H. KIM
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依托单位:
Functional Role of Zebrafish TLR Proteins
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批准号:7860276
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项目类别:
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资助金额:$27.82万
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财政年份:2008
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负责人:CAROL H. KIM
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依托单位:
Functional Role of Zebrafish TLR Proteins
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批准号:8076909
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项目类别:
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资助金额:$27.52万
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财政年份:2008
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负责人:CAROL H. KIM
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依托单位:
Role of CFTR in Toxicant-Sensitivity of Innate Immunity
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批准号:6963707
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项目类别:
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资助金额:$22.28万
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财政年份:2005
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负责人:CAROL H. KIM
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依托单位:
Role of CFTR in Toxicant-Sensitivity of Innate Immunity
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批准号:7140353
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项目类别:
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资助金额:$18.13万
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财政年份:2005
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负责人:CAROL H. KIM
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依托单位:
Toll Signaling Pathway in the Zebrafish
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批准号:6560775
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项目类别:
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资助金额:$14.7万
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财政年份:2001
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负责人:CAROL H. KIM
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依托单位:
Toll Signaling Pathway in Zebrafish Knockdowns
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批准号:6316863
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项目类别:
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资助金额:$14.7万
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财政年份:2001
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负责人:CAROL H. KIM
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依托单位: