Molecular Genetics of Dominant Neovascular Inflammatory Vitreoretinopathy
Molecular Genetics of Dominant Neovascular Inflammatory Vitreoretinopathy
批准号:
8420512
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 retinopathypublic health relevance
中文摘要
描述(由申请人提供):该资助旨在确定与视网膜退行性疾病相关的基因和研究炎症性眼病的NEI研究重点。眼睛是一个具有免疫特权的部位,其局部免疫机制的分子基础尚不清楚。我们描述了一个大家庭,严重的眼内炎症,没有全身特征。基于许多独特的临床特征及其遗传模式,将其命名为常染色体显性新血管炎性玻璃体视网膜病变(ADNIV)。在这种眼睛特有的炎症条件下,基因缺陷触发眼内细胞因子的释放,募集炎症细胞。进行性疾病阶段导致ERG b波丧失、进行性视网膜色素变性、外周视野丧失,最终导致视网膜新生血管形成、视网膜脱离和青光眼。这项资助的具体目的是应用先进的分子遗传学技术来发现ADNIV的致病基因,并应用蛋白质组学技术来识别下游细胞因子信号。我们将利用各种遗传标记策略来缩小连锁间隔,然后通过DNA测序来测试候选基因的突变。眼液样本将用于筛选免疫抑制后疾病各个阶段的细胞因子,并与其他炎症性眼病进行比较。ADNIV基因的发现是非常重要的,因为没有已知的基因专门引起炎症性眼病。此外,ADNIV基因及其效应细胞因子可能与更常见的炎症性眼病有关,如糖尿病视网膜病变、增殖性玻璃体视网膜病变等。确定ADNIV的特定基因突变将是了解眼睛免疫学基本机制的重要一步。这将为炎症性眼病患者提供更有针对性的治疗。ADNIV基因将代表第一个已知的只对眼睛有免疫作用的基因。
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.
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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:8044370
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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