ISOPRENOID METABOLISM IN THE RETINA
ISOPRENOID METABOLISM IN THE RETINA
批准号:
7344693
负责人:
Steven J. Fliesler
金额:
$13.45万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1988
资助国家:
美国
项目状态:
已结题
起止时间:
1988-03-01 至 2008-07-15
关键词:
3-nitrotyrosine4 hydroxynonenal4-hydroxyhexenal7-dehydrocholesterolAY9944AffectAgeAnimal ModelAnimalsAntioxidantsApoptosisAttenuatedBiochemicalBiological AssayBiological ProcessBlindnessCandidate Disease GeneCaspaseCell DeathCholesterolCompatibleConditionCorrelative StudyDefectDiseaseEPC-K1EnzymesExhibitsFunctional disorderFutureGene ExpressionGeneticGenomicsGlycerophospholipidsGoalsHereditary DiseaseHumanIn Situ HybridizationIn Situ Nick-End LabelingInheritedLabelLightLipid PeroxidesLipidsLocalizedMembraneMetabolicMetabolismMethodsMicroarray AnalysisMicroscopyMissionModelingModificationMonitorNecrosisOxidative StressPathway interactionsPatientsPatternPhotoreceptorsPolymerase Chain ReactionProteinsProteomicsQuality of lifeRNARangeRattusResearch PersonnelRetinaRetinalRetinal DegenerationSeriesSmith-Lemli-Opitz SyndromeStagingStandards of Weights and MeasuresSterol Biosynthesis PathwaySterolsSupplementationSyndromeTestingTherapeuticTherapeutic InterventionThioctic AcidTimeTissue-Specific Gene ExpressionTranscriptional RegulationVertebrate PhotoreceptorsVisionVisual impairmentVitamin EWaterWestern Blottingadductage relatedbasecell typecholesterol biosynthesiscytotoxichuman diseaseimmunocytochemistryimprovedinhibitor/antagonistinsightisoprenoidlipid metabolismmouse modeloxidationoxidized lipidpostnatalprogramssex
中文摘要
该项目的长期目标是阐明胆固醇及其相关的生物学功能
英文摘要
The long-range goal of this project is to elucidate the biological functions of cholesterol and related
molecules in the retina. The RSH/Smith-Lemli-Opitz Syndrome (SLOS), involves defective conversion of 7-
dehydrocholesterol (7DHC) to cholesterol. The first discovered in a series of multiple congential anomalies
(MCA) syndromes and anabolic cholesterol pathway defects, it is estimated to be the fourth most common
human recessive disease. SLOS has an associated retinal degeneration, discovered only recently, but the
mechanism underlying the degeneration is unknown. Initial studies suggest the involvement of oxidized
lipids and proteins, as well as "metabolic cross-talk" between sterol metabolism and other pathways, likely
via transcriptional regulation. Treating rats with a selective inhibitor (AY9944) of the same enzyme that is
defective in SLOS affords an animal model that exhibits a progressive retinal degeneration affecting both
rods and cones. Using this model, in comparison with age- and sex-matched control rats, we will employ
three different, complimentary approaches to elucidating the disease mechanism: 1) Microarray analysis
(genomics) will reveal differential gene expression patterns in SLOS rat vs: control retinas, confirming targets
by real-time PCR and biochemical methods. 2) Lipidomics will reveal quantitative differences in the steady-
state levels of normal and oxidized lipids, while 3) proteomics will identify differences in the amounts and
types of specific oxidative modifications of retinal proteins in retinas of these animals. In addition, the
mechanism of photoreceptor cell death will be assessed using standard methods relevant to apoptosis. The
ability of biologically compatible antioxidants (alpha-lipoic acid and EPC-K1) to block lipid and protein
oxidation and to partially ameliorate the retinal degenerationln in SLOS rats will be assessed, under both
normal and "light-damage" conditions. In this way, fundamental new insights into the mechanism of retinal
degeneration associated with SLOS will be obtained. These studies also may provide support for the use of
antioxidants as adjuncts to cholesterol supplementation, the current (if imperfect) therapeutic strategy for
SLOS patient management. The latter has been shown to improve photoreceptor function in the SLOS rat
model. As such, this project supports the NEI's mission of developing sight-saving treatments, reducing
visual impairment and blindness, and improving the quality of life for people of all ages.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Cholesterol homeostasis in the vertebrate retina
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批准号:10580969
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项目类别:
-
资助金额:$39.0万
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财政年份:2023
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负责人:Steven J. Fliesler
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依托单位:
BLRD Research Career Scientist Award Application
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批准号:10512064
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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:2021
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负责人:Steven J. Fliesler
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依托单位:
BLRD Research Career Scientist Award Application
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批准号:10365821
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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:2021
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负责人:Steven J. Fliesler
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依托单位:
Development and characterization of mouse models of RP59 DHDDS deficiency
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批准号:10200065
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项目类别:
-
资助金额:$53.63万
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财政年份:2018
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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:8819205
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项目类别:
-
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:
Ocular Sequelae and Intervention in a Rat Model of Blast Overpressure Polytrauma
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批准号:10082421
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项目类别:
-
资助金额:$0.0万
-
财政年份:2015
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负责人:Steven J. Fliesler
-
依托单位:
Ocular Sequelae and Intervention in a Rat Model of Blast Overpressure Polytrauma
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批准号:10735867
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项目类别:
-
资助金额:$0.0万
-
财政年份:2015
-
负责人:Steven J. Fliesler
-
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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项目类别:
-
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:
-
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:
APOLIPOPROTEIN ISOFORMS AND RETINAL DEGENERATION
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批准号:7683534
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项目类别:
-
资助金额:$6.92万
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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:
-
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:
-
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:
-
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:
-
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
-
依托单位:
BIOMEDICAL RESEARCH SUPPORT GRANT
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批准号:3517644
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项目类别:
-
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:
-
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:
ISOPRENOID METABOLISM IN THE RETINA
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批准号:2838290
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项目类别:
-
资助金额:$31.77万
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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: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
-
负责人:Steven J. Fliesler
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依托单位:
海外基金