Mechanisms of retinal neuronal injury
Mechanisms of retinal neuronal injury
批准号:
9126561
负责人:
Wenbo Zhang
金额:
$38.25万
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-09-30 至 2018-08-31
关键词:
AddressAnimal ModelAnimalsApoptosisAttenuatedBlindnessBlood VesselsBlood flowBone MarrowButyric AcidsCXCL10 geneCXCL11 geneCXCL9 geneCXCR3 geneCell DeathCellsCellular biologyClinicalDataDevelopmentDiabetic RetinopathyDiseaseEndoplasmic ReticulumExtravasationFunctional disorderGene DeletionGeneticGlaucomaHealthcare SystemsIn VitroInflammationInflammatoryInjuryIschemiaLeukocytesLife StressLigandsLinkMediatingMicrogliaModelingMolecularMonitorMusNeuronal InjuryNeuronsOptic Nerve InjuriesOptical Coherence TomographyOutcome StudyOxidative StressOxidative Stress InductionPathway interactionsPatientsPhase I Clinical TrialsPhysiologic Intraocular PressureProductionProteinsQuality ControlQuality of lifeReactionReperfusion TherapyReportingRetinalRetinal DiseasesRetinal Ganglion CellsRetinal Vascular OcclusionRoleSignal TransductionSiteTestingTherapeuticThickTissuesUp-RegulationVisionantiangiogenesis therapycell injurychemokine receptorclinical Diagnosisclinical practicecytokinedesigndiabetic patientendoplasmic reticulum stressin vivo Modelinnovationmonocytemouse modelneovascularizationneuron lossneuroprotectionnovelnovel strategiespreventretinal ischemiaretinal neurontauroursodeoxycholic acid
中文摘要
描述(由申请人提供):视网膜神经元死亡是许多视力威胁疾病的常见病理特征,如糖尿病视网膜病变、视网膜血管阻塞、青光眼、创伤性视神经病变等。这些疾病会导致失明,损害患者的生活质量,并给我们的医疗保健系统带来压力。视网膜神经元损伤是这些疾病的共同病理特征。本研究旨在阐明视网膜病变中神经元损伤的常见机制,并确定新的策略来限制损伤和保护视力。我们将使用不同的视网膜神经元损伤模型来检验我们的新假设,即内质网(ER)应激诱导的CXCL 10表达在视网膜病变期间由于CXCR 3介导的炎症反应和氧化应激诱导引起的视网膜神经元损伤中具有关键作用。我们将使用遗传学和药理学方法来解决以下具体目标:1)确定ER应激在视网膜病变期间增加CXCL 10表达和视网膜神经元损伤中的作用。2)研究CXCL 10/CXCR 3在视网膜病变过程中视网膜神经元损伤中的作用。3)评价通过药物阻断ER应激或CXCR 3的神经保护的治疗益处。这项研究的结果将提供视网膜神经元损伤的新的共同机制,并可能很容易投入到视网膜病变的临床实践。
英文摘要
DESCRIPTION (provided by applicant): Retinal neuronal death is a common pathological feature of many vision threatening diseases, such as diabetic retinopathy, retinal vascular occlusion, glaucoma, traumatic optic neuropathy, and others. These diseases can cause blindness, impair patients' quality of life, and stress our health care system. Retinal neuronal injury is a common pathological feature of these diseases. This study is to delineate the common mechanisms of neuronal injury during retinopathy and identify novel strategies to limit injury and preserve vision. We will use different models of retinal neuronal injury to test our novel hypothesis that endoplasmic reticulum (ER) stress- induced expression of CXCL10 has a key role in retinal neuronal damage due to CXCR3-mediated inflammatory reactions and induction of oxidative stress during retinopathy. We will use genetic and pharmacological approaches to address the following specific aims: 1) Determine the role of ER stress in increasing CXCL10 expression and retinal neuronal injury during retinopathy. 2) Investigate the role of CXCL10/CXCR3 in retinal neuronal injury during retinopathy. 3) Evaluate therapeutic benefits of neuroprotection by pharmacological blockade of ER stress or CXCR3. Outcomes from this study will provide novel common mechanisms of retinal neuronal injury and may be readily put into clinical practice for retinopathy.
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负责人:Wenbo Zhang
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依托单位:
海外基金