Protein Misfolding Diseases and Oxido-Reductive Pathways
Protein Misfolding Diseases and Oxido-Reductive Pathways
批准号:
8537969
负责人:
Ivor James Benjamin
金额:
$72.1万
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:
2009-09-30 至 2015-07-31
关键词:
AwardCardiomyopathiesCellsCessation of lifeClinicalCouplesDiagnosticDiseaseDrosophila genusDrosophila melanogasterExhibitsFunctional disorderGenesGenetic ScreeningGlucosephosphate DehydrogenaseGoalsHeartHeart DiseasesHeart failureHumanHypertrophyImaging TechniquesInheritedLaboratoriesLifeMonitorMusNADPNeurodegenerative DisordersOxidation-ReductionOxidative StressPathway interactionsPatientsReducing AgentsStressStudy modelsSystemTherapeuticThinkingTissuesToxic effectValidationWorkabstractingbiological adaptation to stressdesigneffective therapynovelpreventprotein foldingprotein misfoldingresearch studytherapeutic targettool
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英文摘要
DESCRIPTION
Abstract
Certain inherited modes of heart failure and several neurodegenerative diseases are characterized by protein misfolding states whose underlying mechanism(s) and pathophysiology are poorly understood. Effective therapies exist primarily as goals, not as clinical implementations. Macromolecular damage induced by oxidative stress is the sine qua non for thinking about many diseases. Our laboratory has challenged this paradigm by demonstrating that mouse hearts exhibiting protein-folding cardiomyopathy found in humans are under 'reductive stress' from an over-active antioxidative system. Decreasing the function of glucose-6-phosphate dehydrogenase (G6PD), which generates the reductant NADPH, "cures" the disease in mice by ameliorating reductive stress, aggresome formation, hypertrophy, heart failure and death. This experiment defines a novel causal mechanism and implicates G6PD as a potential therapeutic target. We hypothesize that stress response and anti-oxidative pathways undergo a pathogenic transition, and become dysregulated by macromolecular stresses (e.g., misfolded proteins). We further propose that other cardiac and neurodegenerative diseases result from similar pathogenic transition. Our Pioneer Award proposal is designed to develop a robust experimental platform for exploring the mechanisms of reductive stress disease. Our work will extend from studies that model reductive stress in the genetically amenable fruit fly Drosophila melanogaster, through cultured mouse and human cells, to whole mice, and finally into patients as we work to develop diagnostic tools. Cuttingedge imaging techniques will be developed for monitoring redox couples and toxicities in living cells and tissues. Genetic screens in Drosophila will guide the identification of new genes and determine the effects of potentially therapeutic compounds that prevent reductive stress disease. Validation in mice of interacting genes and pathways will provide us target candidates for pharmacolog
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会议论文
Advancing Student Potential for Inclusion with Research Experiences (ASPIRE)
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批准号:10678356
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项目类别:
-
资助金额:$16.55万
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财政年份:2023
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负责人:Ivor James Benjamin
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依托单位:
Training in Signature Transdisciplinary Cardiovascular Sciences
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批准号:10198992
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项目类别:
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资助金额:$40.76万
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财政年份:2017
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负责人:Ivor James Benjamin
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依托单位:
Training in Signature Transdisciplinary Cardiovascular Sciences
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批准号:10628014
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项目类别:
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资助金额:$54.22万
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财政年份:2017
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负责人:Ivor James Benjamin
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依托单位:
Training in Signature Transdisciplinary Cardiovascular Sciences
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批准号:9209572
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项目类别:
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资助金额:$13.56万
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财政年份:2017
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负责人:Ivor James Benjamin
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依托单位:
Training in Signature Transdisciplinary Cardiovascular Sciences
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批准号:9914120
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项目类别:
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资助金额:$47.75万
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财政年份:2017
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负责人:Ivor James Benjamin
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依托单位:
Conditional HSF1 Expression for Ischemic Cardioprotection
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批准号:7689421
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项目类别:
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资助金额:$0.0万
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财政年份:2009
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负责人:Ivor James Benjamin
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依托单位:
Conditional HSF1 Expression for Ischemic Cardioprotection
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批准号:7786189
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项目类别:
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资助金额:$0.0万
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财政年份:2009
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负责人:Ivor James Benjamin
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依托单位:
Conditional HSF1 Expression for Ischemic Cardioprotection
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批准号:8195885
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项目类别:
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资助金额:$0.0万
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财政年份:2009
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负责人:Ivor James Benjamin
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依托单位:
Protein Misfolding Diseases and Oxido-Reductive Pathways
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批准号:7938819
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项目类别:
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资助金额:$75.21万
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财政年份:2009
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负责人:Ivor James Benjamin
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依托单位:
Protein Misfolding Diseases and Oxido-Reductive Pathways
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批准号:8143267
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项目类别:
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资助金额:$74.0万
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财政年份:2009
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负责人:Ivor James Benjamin
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依托单位:
Protein Misfolding Diseases and Oxido-Reductive Pathways
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批准号:8307817
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项目类别:
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资助金额:$73.98万
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财政年份:2009
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负责人:Ivor James Benjamin
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依托单位:
Conditional HSF1 Expression for Ischemic Cardioprotection
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批准号:8258645
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项目类别:
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资助金额:$0.0万
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财政年份:2009
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负责人:Ivor James Benjamin
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依托单位:
Protein Misfolding Diseases and Oxido-Reductive Pathways
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批准号:7846716
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项目类别:
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资助金额:$75.25万
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财政年份:2009
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负责人:Ivor James Benjamin
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依托单位:
Mechanisms of HSPB2 in Cardiac Metabolism and Ischemic Cardioprotection
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批准号:7475591
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项目类别:
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资助金额:$39.32万
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财政年份:2008
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负责人:Ivor James Benjamin
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依托单位:
Mechanisms of HSPB2 in Cardiac Metabolism and Ischemic Cardioprotection
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批准号:7817180
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项目类别:
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资助金额:$38.1万
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财政年份:2008
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负责人:Ivor James Benjamin
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依托单位:
Mechanisms of HSPB2 in Cardiac Metabolism and Ischemic Cardioprotection
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批准号:8064761
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项目类别:
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资助金额:$38.1万
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财政年份:2008
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负责人:Ivor James Benjamin
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依托单位:
Mechanisms of HSPB2 in Cardiac Metabolism and Ischemic Cardioprotection
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批准号:7617735
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项目类别:
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资助金额:$38.1万
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财政年份:2008
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负责人:Ivor James Benjamin
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依托单位:
HSF 1 Requirements in Extraembryonic Development
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批准号:6536199
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项目类别:
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资助金额:$31.59万
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财政年份:2001
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负责人:Ivor James Benjamin
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依托单位:
HSF 1 Requirements in Extraembryonic Development
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批准号:6755098
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项目类别:
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资助金额:$29.9万
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财政年份:2001
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负责人:Ivor James Benjamin
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依托单位:
HSF 1 Requirements in Extraembryonic Development
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批准号:6918087
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项目类别:
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资助金额:$29.9万
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财政年份:2001
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负责人:Ivor James Benjamin
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依托单位:
海外基金