DICER1 deficiency in aberrant chorioretinal neovascularization - Administrative Supplement OKT Request
DICER1 deficiency in aberrant chorioretinal neovascularization - Administrative Supplement OKT Request
批准号:
10647413
负责人:
Bradley David Gelfand
金额:
$6.02万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2021
资助国家:
美国
项目状态:
未结题
起止时间:
2021-06-01 至 2025-05-31
关键词:
Administrative SupplementAge related macular degenerationAgingAnimalsBlindnessBypassChoroidal NeovascularizationDICER1 geneDevelopmentDiabetic RetinopathyExudative age-related macular degenerationFoundationsGene SilencingGoalsHumanInterventionKnowledgeMediator of activation proteinMedicalMicroRNAsModelingMusOutcomePancreatic ribonucleasePathogenesisPathologicPathologyPathway interactionsProcessPublishingRNARetinaRetinal DiseasesRetinopathy of PrematurityRoleSeveritiesShort Interspersed Nucleotide ElementsTestingage relatedagedimprovedneovascularneovascularizationnovelocular neovascularization
中文摘要
摘要/文摘
英文摘要
SUMMARY/ABSTRACT
Aberrant ocular neovascularization contribute to blindness in numerous conditions including age-related macular
degeneration (AMD), diabetic retinopathy, and retinopathy of prematurity. DICER1 is a RNase that processes
micro-RNAs and SINE RNAs. Deficiency of DICER1 is implicated in outer retinal pathologies, including choroidal
neovascularization. This claim is supported by recently published studies finding that multiple models of DICER1
deficiency develop aberrant choroidal neovascularization in mice, and new evidence that DICER1 expression is
significantly reduced in human neovascular AMD. However, major gaps in knowledge persist with respect to the
relative contributions of major DICER1 substrate classes micro-RNA and SINE RNA imbalances as contributors
to choroidal neovascularization. In addition, whether DICER1 deficiency impedes conventional gene silencing
strategies, and the role of DICER1 in age-related neovascular pathologies are unknown. The overall hypothesis
of this project is that age-related DICER1 deficiency drives chorioretinal neovascularization via SINE RNA
accumulation and impedes conventional gene silencing strategies. We will test this hypothesis in three specific
aims. 1) We will distinguish between the contributions of micro-RNA and SINE RNA-dependent processing
activities of DICER1 with respect to development and severity of CNV. 2) We will adapt DICER1-independent
gene silencing strategies and compare them to traditional DICER1-dependent strategies in models of CNV. 3)
We will quantify DICER1 in aging retina, and determine whether ectopic DICER1 expression improves CNV
outcomes in aged animals. Collectively, these thematically related, but independent aims will establish new
foundational and translationally relevant knowledge about the mediators and consequences of DICER1
deficiency in pathological choroidal neovascularization. These studies may thereby open new interventional
avenues for prevalent blinding conditions.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Mechanistic basis of sexual dimorphism in antigen-independent IgG1 angiogenesis regulation
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批准号:10660051
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项目类别:
-
资助金额:$68.99万
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财政年份:2023
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负责人:Bradley David Gelfand
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依托单位:
DICER1 deficiency in aberrant chorioretinal neovascularization
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批准号:10407583
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项目类别:
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资助金额:$49.5万
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财政年份:2021
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负责人:Bradley David Gelfand
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依托单位:
DICER1 deficiency in aberrant chorioretinal neovascularization
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批准号:10624267
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项目类别:
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资助金额:$51.04万
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财政年份:2021
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负责人:Bradley David Gelfand
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依托单位:
DICER1 deficiency in aberrant chorioretinal neovascularization
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批准号:10183845
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项目类别:
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资助金额:$52.57万
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财政年份:2021
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负责人:Bradley David Gelfand
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依托单位:
海外基金