APOLIPOPROTEIN ISOFORMS AND RETINAL DEGENERATION
APOLIPOPROTEIN ISOFORMS AND RETINAL DEGENERATION
批准号:
7683534
负责人:
Steven J. Fliesler
金额:
$6.92万
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-02-01 至 2009-07-31
关键词:
AddressAgeAge related macular degenerationAllelesAlzheimer&aposs DiseaseAnimal ModelApolipoprotein EApolipoproteinsAstrocytesBiological ModelsBiologyBlindnessBrainBreedingCellsCholesterol HomeostasisCommunitiesDementiaDevelopmentDiseaseElderlyElectron MicroscopyElectroretinographyExhibitsEye diseasesFutureGenerationsGenesGeneticGenotypeGlial Fibrillary Acidic ProteinGoalsHealthHistologyHumanIncidenceInheritedKnowledgeLightMethodsMissionModelingMolecularMouse StrainsMusMutant Strains MiceMutationNeuraxisNeurodegenerative DisordersNeurogliaPharmacologic SubstancePlayPolymerase Chain ReactionPrincipal InvestigatorProtein IsoformsProteinsQuality of lifeRangeRecoveryResearchResourcesRetinaRetinalRetinal DegenerationRisk FactorsRoleSeveritiesTestingTherapeutic InterventionThinkingTimeTransgenic MiceTransgenic OrganismsVisual impairmentVisual system structureWestern Blottingapolipoprotein E-3apolipoprotein E-4basecentral nervous system injuryclinically relevantdisorder riskimmunocytochemistryimprovedlight microscopymorphometrynovelpostnatalpreventprogramspromoterselective expressiontrend
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The long-range goal of this study is to understand the biology of apolipoproteins in the retina, particularly the mechanism by which specific apoE isoforms may exert (or lack) neuroprotective effects. The immediate goal of this 2-year exploratory project is to develop and characterize the requisite genetically altered mouse strains to pursue the long-range goal. ApoE is a protein involved in cholesterol metabolism and transport. In the brain, the apoES isoform is thought to be neuroprotective and to play an important role in recovery following CNS injury. In contrast, the apoE4 isoform is a risk factor for dementias, such as Alzheimer's disease. Paradoxically, the exact opposite trend seems to prevail in age-related macular degeneration (AMD), where apoE4 correlates with reduced incidence of disease. The reason for this paradox remains a mystery, and will require appropriate new model systems to elucidate the molecular mechanisms involved. As a first step toward that goal, we will develop novel mouse strains and assess whether apoE can modulate the severity and time course of hereditary retinal degeneration in an isoform-specific manner. Mutant mice harboring the rds (retinal degeneration slow) mutation and lacking the apoE gene will be cross-bred with mice that selectively express either the human apoES or apoE4 isoform. Genotype will be confirmed by PCR. ApoE expression will be assessed as a function of age using Western blot analysis and immunocytochemistry, in comparison with age-matched rds and non-transgenic (wild-type) control mice. Retinal degeneration will be assessed by light and electron microscopy; retinal function will be assessed by electroretinography (ERG). The clinical relevance of this study lies in the potential to modulate the expression of neuroprotective isoforms of apoE in the retina as a novel therapy to retard or ameliorate human retinal degenerations of various origins. As such, this project has the potential to impact several aspects of the NEI's mission: to help prevent and treat eye diseases and other disorders of vision; reduce visual impairment and blindness; improve the quality of life for people of all ages; and advance our knowledge of how the visual system functions in health and disease.
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Cholesterol homeostasis in the vertebrate retina
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财政年份:2015
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负责人:Steven J. Fliesler
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依托单位:
Ocular Sequelae and Intervention in a Rat Model of Blast Overpressure Polytrauma
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批准号:10082421
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财政年份:2015
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依托单位:
Ocular Sequelae and Intervention in a Rat Model of Blast Overpressure Polytrauma
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资助金额:$0.0万
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负责人:Steven J. Fliesler
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依托单位:
Ocular Sequelae and Intervention in a Rat Model of Blast Overpressure Polytrauma
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批准号:10361397
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资助金额:$0.0万
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财政年份:2015
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负责人:Steven J. Fliesler
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依托单位:
APOLIPOPROTEIN ISOFORMS AND RETINAL DEGENERATION
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批准号:7229831
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项目类别:
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资助金额:$15.24万
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财政年份:2006
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负责人:Steven J. Fliesler
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依托单位:
APOLIPOPROTEIN ISOFORMS AND RETINAL DEGENERATION
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批准号:7014983
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项目类别:
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资助金额:$18.38万
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财政年份:2006
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负责人:Steven J. Fliesler
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依托单位:
SMALL INSTRUMENTATION GRANT
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批准号:2165063
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项目类别:
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资助金额:$1.11万
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财政年份:1994
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负责人:Steven J. Fliesler
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依托单位:
ANIMAL FACILITY IMPROVEMENT FOR SMALL RESEARCH PROGRAM
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批准号:3059330
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项目类别:
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资助金额:$25.0万
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财政年份:1993
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负责人:Steven J. Fliesler
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依托单位:
SMALL INSTRUMENTATION GRANT
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批准号:3524571
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项目类别:
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资助金额:$0.72万
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财政年份:1993
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负责人:Steven J. Fliesler
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依托单位:
SMALL INSTRUMENTATION GRANT
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批准号:3524561
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项目类别:
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资助金额:$0.84万
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财政年份:1992
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负责人:Steven J. Fliesler
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依托单位:
ANIMAL FACILITY IMPROVEMENT FOR SMALL RESEARCH PROGRAM
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批准号:3059300
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项目类别:
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资助金额:$20.52万
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财政年份:1992
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负责人:Steven J. Fliesler
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依托单位:
BIOMEDICAL RESEARCH SUPPORT GRANT
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批准号:3517644
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项目类别:
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资助金额:$0.61万
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财政年份:1991
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负责人:Steven J. Fliesler
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依托单位:
SMALL INSTRUMENTATION GRANT
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批准号:3524484
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项目类别:
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资助金额:$0.5万
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财政年份:1990
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负责人:Steven J. Fliesler
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依托单位:
GLYCOPROTEIN SYNTHESIS AND METABOLISM IN RETINA
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批准号:3261981
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项目类别:
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资助金额:$16.11万
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财政年份:1988
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负责人:Steven J. Fliesler
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依托单位:
GLYCOPROTEIN SYNTHESIS AND METABOLISM IN RETINA
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批准号:2159735
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项目类别:
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资助金额:$10.95万
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财政年份:1988
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负责人:Steven J. Fliesler
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依托单位:
GLYCOPROTEIN SYNTHESIS AND METABOLISM IN RETINA
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批准号:2159737
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项目类别:
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资助金额:$27.35万
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财政年份:1988
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负责人:Steven J. Fliesler
-
依托单位:
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