In vivo role of BTK-mediated inhibition of Wnt/b-catenin signaling during hematop
In vivo role of BTK-mediated inhibition of Wnt/b-catenin signaling during hematop
批准号:
8514128
负责人:
Richard Goff James
金额:
$24.9万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-08-14 至 2015-05-31
关键词:
AdultAmino AcidsAnimal Disease ModelsAreaAttentionAwardB-LymphocytesBasic ScienceBiological ModelsBlood CellsBone MarrowBone Marrow TransplantationCancer cell lineCell Culture TechniquesCell LineCellsChemicalsClinicalColorectal CancerDataDevelopmentDiagnosisEmbryoEngraftmentEventFlow CytometryGalactosidaseGene TargetingGenetic SuppressionHematopoiesisHematopoietic SystemHematopoietic stem cellsHome environmentHumanInvestigationKnowledgeLarge Intestine CarcinomaLearningMass Spectrum AnalysisMediatingMethodsMissionModelingMolecularMonitorMusMutationNational Heart, Lung, and Blood InstitutePathway interactionsPatientsPeptidesPhosphorylationPositioning AttributeProteomicsRegulationReporterResearch PersonnelRoleSamplingSignal PathwaySignal TransductionSmall Interfering RNASorting - Cell MovementSpleenStable Isotope LabelingStem cellsSymptomsTEC Protein Tyrosine KinaseTechniquesTestingTrainingUmbilical Cord BloodUmbilical cord structureWorkX-Linked AgammaglobulinemiaZebrafishabstractingbasecancer therapychemical geneticsgain of functionimprovedin vitro Modelin vivointerestkinase inhibitorloss of functionpost-doctoral trainingreconstitutionresearch studysmall moleculetissue culture
中文摘要
项目摘要
目前,我正在使用化学遗传学,siRNA筛选和质谱-
基于蛋白质组学来探测Wnt/β-catenin信号通路。使用这些
技术,我们确定Tec激酶作为Wnt/β-连环蛋白的负调节因子
信号因为Tec激酶BTK中的突变负责X连锁的
在无丙种球蛋白血症中,我们试图证实我们在B细胞中的原始发现。
我们发现Tec激酶在B细胞中也负调节Wnt/β-catenin信号传导
细胞培养。这项工作使我提出了一个假设,即Tec
激酶和Wnt信号传导在体内造血中具有重要作用。我
我申请独立之路奖,以延长我的
博士后培训,这样我就可以了解疾病的动物模型,
造血和获得如何解剖小鼠和收集
骨髓,如何进行小鼠骨髓移植实验
以及如何通过流式细胞术分析这些实验。中概述的
为了验证我的假设,我将使用所有这些方法。作为
独立调查员我计划利用我在
蛋白质组学和造血,探讨信号的分子机制
细胞分化中的转导。这个方向不仅能让我
充分利用我迄今为止的训练,这将使我进入一个领域,
重要的临床意义,如脐带血移植,骨髓
移植和癌症治疗。
英文摘要
Project Abstract
Currently I am using chemical genetics, siRNA screens and mass spectrometry-
based proteomics to probe the Wnt/ -catenin signaling pathway. Using these
techniques we identified Tec kinases as negative regulators of Wnt/ -catenin
signaling. Because mutations in the Tec kinase BTK are responsible for X-linked
agammaglobulinemia, we sought to corroborate our original findings in B cells.
We found that Tec kinases also negatively regulate Wnt/ -catenin signaling in B
cells in culture. This work has led me to the hypothesis that the interplay of Tec
kinases and Wnt signaling will have a significant role in hematopoiesis in vivo. I
am applying for the Pathway to Independence Award in order to extend my
postdoctoral training so that I can learn about animal models of disease and
hematopoiesis and gain practical knowledge of how to dissect mice and collect
bone marrow, how to perform murine bone marrow transplantation experiments
and how to analyze these experiments by flow cytometry. As outlined in the
proposal, I will use all of these methods in order to test my hypothesis. As an
independent investigator I plan to exploit my unique position at the intersection of
proteomics and hematopoiesis to explore the molecular mechanisms of signal
transduction in cellular differentiation. Not only would this direction allow me to
fully utilize my training to date, it would allow me to enter a field that has
important clinical implications, such as cord blood engraftment, bone marrow
transplant and cancer treatments.
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专著(0)
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会议论文
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依托单位:
海外基金