Molecular Genetics of Dominant Neovascular Inflammatory Vitreoretinopathy
Molecular Genetics of Dominant Neovascular Inflammatory Vitreoretinopathy
批准号:
8044370
负责人:
Vinit B Mahajan
金额:
$22.79万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-02-01 至 2016-01-31
关键词:
11q13AddressAffectBlindnessCandidate Disease GeneCataractCellsChromosomesClinicalCopy Number PolymorphismCystoid Macular EdemaCytokine SignalingDNADNA SequenceDefectDegenerative DisorderDiabetic RetinopathyDiseaseDisease modelDominant Genetic ConditionsEyeEye diseasesFamilyFeedbackFibrosisGene DeletionGene MutationGenesGenetic MarkersGenetic PolymorphismGenetic TechniquesGlaucomaGrantHaplotypesImmuneImmunologyImmunosuppressionInflammationInflammatoryInheritance PatternsInheritedIowaIrisLaboratory FindingLeadLeukocytesLinkLiquid substanceMapsMediatingMolecular GeneticsNamesPatientsPeripheral Retinal DegenerationPhenotypePosterior UveitisProgressive DiseaseProliferative VitreoretinopathyProteomicsRecruitment ActivityResearch PriorityRetinalRetinal DegenerationRetinal DetachmentRetinal EdemasRetinal NeovascularizationRetinitis PigmentosaSamplingShort Tandem RepeatSignal TransductionSingle Nucleotide PolymorphismStagingTechniquesTestingTranslatingUniversitiesUveitisVitreous Hemorrhageadvanced diseasebasecytokinedisease-causing mutationextracellulargene discoverygenetic pedigreemembermolecular siteneovascularneovascularizationproliferative diabetic retinopathy
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): This grant addresses NEI research priorities to identify the genes involved in retinal degenerative diseases and study inflammatory eye disease. The eye is an immune privileged site where the molecular basis of local immunological mechanisms is poorly understood. We characterized a large family with severe intraocular inflammation and no systemic features. Based on a number of unique clinical features and its pattern of inheritance, it was named Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy (ADNIV). In this eye-specific, inflammatory condition, a gene defect triggers the release of intraocular cytokines that recruit inflammatory cells. Progressive disease stages lead to loss of the ERG b-wave, progressive pigmentary retinal degeneration, peripheral field loss, and eventually retinal neovascularization, retinal detachment, and glaucoma. The specific aims of this grant are to apply advanced molecular genetic techniques to discover the causative gene for ADNIV and proteomic techniques to identify downstream cytokine signals. We will utilize a variety of genetic marker strategies to narrow the linkage interval and then test candidate genes for mutations by DNA sequencing. Eye fluid samples will be used to screen for cytokines at various stages of disease, following immunosuppression, and in comparison to other inflammatory eye diseases. Discovery of the ADNIV gene is highly significant, since there are no known genes that exclusively cause inflammatory eye disease. Moreover, the ADNIV gene and its effector cytokines may be linked to more common inflammatory eye diseases, such as diabetic retinopathy, proliferative vitreoretinopathy, and Relevance. Identifying the specific gene mutation for ADNIV will represent an important step towards understanding the basic mechanisms of eye immunology. This will allow for more targeted therapy for patients with inflammatory eye disease. The ADNIV gene will represent the first known gene with immunological effects exclusive to the eye.
PUBLIC HEALTH RELEVANCE: ADNIV is an inherited eye disease that shares a number of features with more common eye diseases such as diabetic retinopathy, intraocular inflammation, and retinal detachment, and retinal detachment. Discovery of the gene and downstream signals in this disease will help to understand and treat these blinding diseases.
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会议论文
FASEB SRC: The Biology of Calpains in Health and Disease
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批准号:10463281
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项目类别:
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资助金额:$3.0万
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财政年份:2022
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负责人:Vinit B Mahajan
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依托单位:
Mechanism-based therapies for photoreceptor degeneration
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批准号:9262938
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项目类别:
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资助金额:$11.92万
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财政年份:2015
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负责人:Vinit B Mahajan
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依托单位:
Mechanism-based therapies for photoreceptor degeneration
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批准号:8856737
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项目类别:
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资助金额:$31.69万
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财政年份:2015
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负责人:Vinit B Mahajan
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依托单位:
Molecular Genetics of Dominant Neovascular Inflammatory Vitreoretinopathy
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批准号:8212205
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项目类别:
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资助金额:$22.79万
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财政年份:2011
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负责人:Vinit B Mahajan
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依托单位:
Molecular Genetics of Dominant Neovascular Inflammatory Vitreoretinopathy
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批准号:8420512
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项目类别:
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资助金额:$22.79万
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财政年份:2011
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负责人:Vinit B Mahajan
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依托单位:
Signal Transduction Mechanisms in Ocular Albinism
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批准号:6718310
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项目类别:
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资助金额:$9.41万
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财政年份:2004
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负责人:Vinit B Mahajan
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依托单位:
海外基金