Cell Physiology Core
Cell Physiology Core
批准号:
9894838
负责人:
BIMAL N. DESAI
金额:
$31.69万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至
关键词:
AntibodiesApoptoticBiological AssayBlood CellsBlood VesselsCRISPR/Cas technologyCell LineCell membraneCell physiologyCellsCuesDevelopmentDiseaseDyesElectrophysiology (science)EquipmentEvaluationFlow CytometryFluorescent DyesGenerationsGenesGoalsGoldHumanIndividualInflammationIon ChannelMeasurementMeasuresMediatingMethodsMissionMusPathologicPhysiologicalPhysiologyReagentReproducibilityResearchServicesSignal TransductionSignaling MoleculeStandardizationSystemTO-PRO-3TechniquesTrainingVariantcardiometabolismdata qualitydesigninnovationmouse modelnovelpatch clampprogramsresponsesmall moleculetooluptakevascular inflammation
中文摘要
点击翻译按钮获取中文摘要
英文摘要
CORE C PROJECT SUMMARY
Pannexin 1 (Panx1) forms plasma membrane ion channels that release important intercellular signalling
molecules, specifically ATP and UTP, under pathological and physiological conditions; the channels also support
uptake of various fluorescent dyes that have traditionally been used to mark apoptotic cells (e.g., YO-PRO-1,
TO-PRO-3). In this PPG application, novel mouse models are employed to ascertain contributions of Panx1-
mediated ATP/UTP release, (and other metabolite release, when needed) to various aspects of cardiometabolic
diseases, and to understand corresponding mechanisms of Panx1 channel activation. Cell Physiology Core
centralizes the functional analysis of Pannexin channels by absorbing, optimizing and standardizing the key
assays of universal significance to all four projects. These include: (1) Analysis of Panx1 channel function in
primary cells by electrophysiology and dye uptake assays and; (2) Electrophysiological characterization of novel
small molecule modulators of Pannexin channels. Similarly, the core also takes the initiative in the development
of innovative tools and methods that can provide a clear technical edge to the entire research program. This
includes generation of novel Panx1 variants and gene-edited mouse lines, generated by CRISPR/Cas9
technology. In executing these centralized goals, often of salience to the entire research program, the core
recognizes the paramount importance of data quality and reproducibility. For the vertical and horizontal
integration proposed in this PPG, this core sits at the interface between cellular and systems levels of analysis
of Panx1 function.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Mitochondrial Calcium Signaling in Cell Intrinsic Immunity
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批准号:10620267
-
项目类别:
-
资助金额:$56.07万
-
财政年份:2021
-
负责人:BIMAL N. DESAI
-
依托单位:
Mitochondrial Calcium Signaling in Cell Intrinsic Immunity
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批准号:10297192
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项目类别:
-
资助金额:$56.07万
-
财政年份:2021
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负责人:BIMAL N. DESAI
-
依托单位:
Mitochondrial Calcium Signaling in Cell Intrinsic Immunity
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批准号:10424585
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项目类别:
-
资助金额:$56.07万
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财政年份:2021
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负责人:BIMAL N. DESAI
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依托单位:
TRPM7 at the Crossroads of Tissue Homeostasis and inflammation
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批准号:10409807
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项目类别:
-
资助金额:$36.8万
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财政年份:2016
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负责人:BIMAL N. DESAI
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依托单位:
The regulation and function of TRPM7 in inflammation
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批准号:9198955
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项目类别:
-
资助金额:$35.55万
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财政年份:2016
-
负责人:BIMAL N. DESAI
-
依托单位:
TRPM7 at the Crossroads of Tissue Homeostasis and inflammation
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批准号:10210717
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项目类别:
-
资助金额:$44.02万
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财政年份:2016
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负责人:BIMAL N. DESAI
-
依托单位:
TRPM7 at the Crossroads of Tissue Homeostasis and inflammation
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批准号:10569632
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项目类别:
-
资助金额:$36.8万
-
财政年份:2016
-
负责人:BIMAL N. DESAI
-
依托单位:
The regulation and function of TRPM7 in inflammation
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批准号:9028940
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项目类别:
-
资助金额:$35.55万
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财政年份:2016
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负责人:BIMAL N. DESAI
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依托单位:
Cell Physiology Core
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批准号:10407612
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项目类别:
-
资助金额:$31.48万
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财政年份:2014
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负责人:BIMAL N. DESAI
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依托单位:
Cell Physiology Core
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批准号:10200121
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项目类别:
-
资助金额:$31.48万
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财政年份:2014
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负责人:BIMAL N. DESAI
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依托单位:
Cell Physiology Core
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批准号:10625323
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项目类别:
-
资助金额:$31.48万
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财政年份:2014
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负责人:BIMAL N. DESAI
-
依托单位:
Cell Physiology Core
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批准号:8787177
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项目类别:
-
资助金额:$30.73万
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财政年份:--
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负责人:BIMAL N. DESAI
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依托单位:
Cell Physiology Core
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批准号:9059169
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项目类别:
-
资助金额:$30.73万
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财政年份:--
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负责人:BIMAL N. DESAI
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依托单位:
海外基金