Ligatable fluorescent probes using energy transfer for apoptosis detection
Ligatable fluorescent probes using energy transfer for apoptosis detection
批准号:
8048999
负责人:
VLADIMIR V DIDENKO
金额:
$23.03万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-04-01 至 2013-03-31
关键词:
Alzheimer&aposs DiseaseApoptosisApoptoticBiochemistryBiological AssayBrainBrain IschemiaCaspaseCell Culture TechniquesCell DeathCellsCerebral IschemiaClinical PathologyClinical ResearchColorDNADNA DamageDNA Double Strand BreakDetectionDevelopmentDevicesDiagnosticDiscriminationDiseaseEnergy TransferEvaluationExperimental ModelsExperimental PathologyFibroblastsFluorescenceFluorescence Resonance Energy TransferFluorescent ProbesImageryIn SituInterventionLabelLifeLigationMalignant NeoplasmsMediatingMedicalMethodologyMethodsModelingMolecularMolecular TargetNecrosisNeuronsOligonucleotide ProbesPathologyPropertyRattusReactionResearchSamplingSpecificityStrokeT4 DNA LigaseTechniquesTechnologyTestingTherapeutic InterventionTimeTissue SampleTissuesWorkcell typecellular imagingneuronal survivalnovelnovel strategiesnucleaseprognosticprogramspublic health relevanceresearch studytissue fixing
中文摘要
描述(由申请人提供):该项目将引入一种新的原位检测凋亡细胞的方法。该方法将适用于固定组织样本和活细胞培养。它将检测由caspase依赖和caspase非依赖机制驱动的细胞凋亡。该方法将使用荧光能量转移(FET)寡核苷酸探针来检测caspase依赖和非依赖的凋亡核酸酶产生的末端为3‘OH/5’PO4的DNA钝端切割。这些切片代表了坏死中缺乏的细胞凋亡的选择性和一般性的标志。FET探头将通过改变颜色来指示成功检测到其目标中断。这种新的细胞凋亡标记技术将使更灵敏的细胞凋亡检测和区分程序性和非程序性细胞死亡成为可能。该提案的具体目的是:1)利用荧光能量转移探针和T4 DNA连接酶,开发一种新的通用的细胞凋亡检测技术,该技术将选择性地标记各种凋亡执行核酸酶共同的特定类型的钝端DNA断裂。用几种细胞凋亡和坏死的模型在固定的组织切片上测试这些探针。2)将目标1中发展的方法学扩展到活细胞培养。利用细胞培养的细胞凋亡和坏死模型,验证不同类型的凋亡细胞死亡的选择性标记及其与坏死的区别。3)验证新方法的有效性,将其应用于同时存在坏死和多种细胞凋亡的局灶性脑缺血的研究。目的:探讨实验性卒中大鼠脑内细胞凋亡性和坏死性死亡的始动和动态。拟议的研究将引入新的使能技术,这对广泛的临床和研究研究非常重要。它在脑缺血中的应用将为开发精确和有效的治疗干预措施提供必要的信息。
公共卫生相关性:拟议的项目将导致开发一种新的分析方法,以满足医疗诊断和病理学的需要。这项技术将允许准确评估细胞死亡和DNA损伤具有预后价值的疾病的治疗效果,如中风、阿尔茨海默病和各种癌症。
英文摘要
DESCRIPTION (provided by applicant): This project will introduce a new approach for in situ detection of apoptotic cells. The approach will be applicable to fixed tissue samples and to live cell cultures. It will detect apoptosis driven by caspase- dependent and caspase-independent mechanisms. The approach will use fluorescence energy transfer (FET) oligoprobes to detect blunt ended DNA cuts with terminal 3'OH/5'PO4 produced by caspase-dependent and -independent apoptotic nucleases. These cuts represent a selective and general marker of apoptosis absent in necrosis. The FET probes will indicate successful detection of their target breaks by changing color. This new apoptosis labeling technology will make possible more sensitive apoptosis detection and discrimination between programmed and non-programmed cell death. The Specific Aims of the proposal are: 1) To develop a new and general apoptosis detection technology using fluorescence energy transfer probes and T4 DNA ligase, which will selectively label a specific type of blunt-ended DNA breaks common for various apoptotic executioner nucleases. To test the probes in fixed tissue sections using several models of apoptosis and necrosis. 2) To expand the methodology developed in the Aim 1 to live cell cultures. To verify selective labeling of different types of apoptotic cell death and its discrimination from necrosis using cell culture models of apoptosis and necrosis. 3) To validate the new approach by applying it to study focal cerebral ischemia as a condition where necrosis and several types of apoptosis are simultaneously present. To investigate the initiation and dynamics of apoptotic and necrotic cell death in brain after experimental stroke in rats. The proposed research will introduce the new enabling technology important for a wide range of clinical and research studies. Its application to brain ischemia will provide information essential for the development of precise and effective therapeutic interventions.
PUBLIC HEALTH RELEVANCE: The proposed project will result in the development of a new assay for the needs of medical diagnostics and pathology. The technology will allow precise evaluation of the effects of therapy in diseases where cell death and DNA damage have prognostic value, such as stroke, Alzheimer's disease, and various cancers.
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