Investigating the role of Tumor Necrosis Factor-Receptor Associated Factor 3 Interacting Protein 2
Investigating the role of Tumor Necrosis Factor-Receptor Associated Factor 3 Interacting Protein 2
批准号:
9923812
负责人:
Shaoping Zhang
金额:
$24.9万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-07-01 至 2022-06-30
关键词:
16S ribosomal RNA sequencingAdaptor Signaling ProteinAddressAdultAffectAllelesAlveolar Bone LossBiological AssayBiologyCRISPR/Cas technologyCellsClinicalCo-ImmunoprecipitationsCodeComplexDataDefectDefense MechanismsDevelopmentDiabetes MellitusDiagnosticDiseaseEnvironmentEnzyme-Linked Immunosorbent AssayEpithelialEpithelial CellsExhibitsFacultyFeedbackFlow CytometryFluorescenceFosteringFunctional disorderFundingGenesGeneticGenetic EngineeringGenetic TranscriptionGenomicsGingivaGoalsHealthHomeostasisHumanIL17 Signaling PathwayIL17 geneImmuneImmune responseImmunobiologyImmunologic MonitoringImmunoprecipitationIn VitroInflammationInflammatoryInflammatory ResponseInterleukin-17InterventionIntestinesKnock-outKnockout MiceKnowledgeLinkage DisequilibriumMediatingMentorshipMessenger RNAModelingMolecularMouth DiseasesMucosal Immune ResponsesMucous MembraneMusNecrosisNeutrophil InfiltrationNorth CarolinaOralOral healthPathway interactionsPatientsPeriodontal DiseasesPeriodontitisPharmacologyPhasePhenotypePlayPopulationPorphyromonas gingivalisPositioning AttributePost-Transcriptional RegulationPreventivePreventive treatmentProductionProteinsRNARegulationResearch PersonnelResearch ProposalsRoleScientistSignal PathwaySignal TransductionStructureSurfaceSystemic diseaseTNF Receptor-Associated FactorsTNF geneTRAF2 geneTRAF6 geneTestingTherapeuticTight JunctionsTissuesTooth LossTracerTrainingTranscriptional ActivationTranscriptional RegulationUnited StatesUniversitiesUpdateVariantWild Type Mousecareercareer developmentchemokinecytokinedysbiosisgenetic approachgenetic variantgenome wide association studyimplementation researchimprovedin vivoindividualized medicineinterestinterleukin-22knock-downloss of functionmRNA StabilitymembermicroCTmicrobialmicrobial communitymicrobial hostmicrobiomeneutrophilnoveloccludinpathogenpathogenic bacteriaperiodontopathogenpreclinical studypreventreceptorrecruitresponserisk varianttenure tracktool
中文摘要
项目总结
候选人是一名双重训练的牙周病科学家,致力于致力于
研究牙周病,改善口腔健康。牙周炎是一种多基因的炎性反应。
对牙龈表面的细菌病原体,影响美国47%的成年人
各州。这种常见的口腔疾病,如果没有有效的治疗,最终会导致牙齿脱落,并
与糖尿病等全身性疾病显著相关。一种全基因组关联分析
牙周炎研究发现肿瘤坏死因子受体相关因子3相互作用
蛋白2(TRAF3IP2)作为目的基因。TRAF3IP2功能障碍等关键基因引起
变异与高致病菌定义的牙周炎表型显著相关
TRAF3IP2是IL-17途径中的一个非冗余接头分子,
它在粘膜防御中起着关键作用。这项研究计划的目的是获取知识
TRAF3IP2介导的IL-17在牙龈屏障防御机制中的应答及其变异体诱导
IL-17途径的功能缺陷。候选假设TRAF3IP2-IL17信令丢失
损害口腔上皮屏障和粘膜炎症信号,促进反生菌
微生物群过度生长。这一假说将通过体外和体内遗传学方法进行验证。vbl.使用
Traf3ip2消融小鼠后,候选者将首先确定IL-17/TRAF3IP2途径的调控作用
牙周病原体诱导的小鼠牙槽骨的免疫反应和微生物群落结构
损失模型(Aim1)。然后,候选人将研究IL-17/TRAF3IP2途径在粘膜中的作用
IL-17调节紧密连接结构的物理屏障功能和机制(目标2)。候选人将会
进一步确定TRAF3IP2变异体对免疫应答的影响,其反映在转录和
基因工程人趋化因子合成和屏障功能的转录后调控
牙龈上皮细胞(AIM 3)。这项研究计划的实施需要额外的培训。
包括复合微生物群落结构分析、Th17/IL-17免疫生物学、上皮生物学和
分子基因组学。各领域专家的强大指导和
北卡罗来纳大学教堂山分校将促进这项研究提案的完成,并
加快应聘者的职业发展。其中概述的科学组成部分和培训
提案提供了一条途径,不仅可以实现候选人的短期目标,也就是过渡到
在终身教职跟踪教员职位上担任独立研究员,获得R01资金支持,但也是长期的
目标是更新对粘膜表面宿主-病原体相互作用的理解。专业知识
所取得的成果将有助于开发新的预防、诊断和治疗手段
改善牙周疾病,改善口腔健康。
英文摘要
PROJECT SUMMARY
The candidate is a dual-trained periodontist scientist who is committed to an academic career dedicated to
study periodontal disease and improve oral health. Periodontitis is a polygenetic, inflammatory response
towards bacterial pathogens at the gingival surface and affects 47% of the adult population in the United
States. This common oral disease, without effective management, eventually leads to tooth loss and is
significantly associated with systemic conditions such as diabetes. Analysis of a Genome Wide Association
Study (GWAS) for periodontitis has identified Tumor necrosis factor Receptor-Associated Factor 3 Interacting
Protein 2 (TRAF3IP2) as a target gene of interest. TRAF3IP2 dysfunction, such as induced by key genetic
variants, is significantly associated with a periodontal inflammation phenotype defined by a high pathogen
burden in plaque and local inflammation.TRAF3IP2 is a non-redundant adaptor molecule in the IL-17 pathway,
which plays a critical role in mucosal defense. The objective of this research proposal is to acquire knowledge
of the TRAF3IP2-mediated IL-17 response in gingival barrier defense mechanisms and the variant-induced
functional defects in the IL-17 pathway. The candidate hypothesizes that loss of TRAF3IP2-IL17 signaling
compromises the oral epithelial barrier and mucosal inflammatory signature and promotes dysbiotic
microbiome overgrowth. This hypothesis will be tested by both in vitro and in vivo genetic approaches. Using
Traf3ip2 ablated mice, the candidate will first determine the role of the IL-17/TRAF3IP2 pathway-modulated
immune response and microbial community structure in a periodontal pathogen-induced murine alveolar bone
loss model (Aim1). The candidate will then investigate the role of the IL-17/TRAF3IP2 pathway in mucosal
physical barrier function and mechanism of IL-17-regulated tight junction structure (Aim 2). The candidate will
further determine the TRAF3IP2 variant effect on immune response as reflected by the transcriptional and
post-transcriptional regulation of chemokine synthesis and barrier function in genetically engineered, human
gingival epithelial cells (Aim 3). The implementation of this research proposal requires additional training
including complex microbial community structure analysis, Th17/IL-17 immunobiology, epithelial biology and
molecular genomics. Strong mentorship by experts in each field and the exceptional environment at the
University of North Carolina at Chapel Hill will foster the accomplishment of this research proposal and
expedite the career development of the candidate. The scientific component and training outlined in this
proposal provide a pathway to achieving not only the candidate's short-term goal, which is to transition into an
independent investigator at a tenure track faculty position with R01 funding support, but also the long-term
goal, which is to update understanding of host-pathogen interactions at the mucosal surface. The expertise
gained will facilitate the development of novel preventive, diagnostic and therapeutic means to tackle
periodontal disease and improve oral health.
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会议论文
Assessing the role of Type I Interferon (IFN-I) in Periodontal Disease
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批准号:10558868
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项目类别:
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资助金额:$38.88万
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财政年份:2023
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负责人:Shaoping Zhang
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依托单位:
Investigating the role of Tumor Necrosis Factor-Receptor Associated Factor 3 Interacting Protein 2
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批准号:10180936
-
项目类别:
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资助金额:$24.11万
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财政年份:2019
-
负责人:Shaoping Zhang
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依托单位: