Investigating the role of the R213G SOD3 polymorphism in lung disease
Investigating the role of the R213G SOD3 polymorphism in lung disease
批准号:
8371183
负责人:
RUSSELL Paul BOWLER
金额:
$27.16万
依托单位:
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:
2012-07-01 至 2016-04-30
关键词:
AcuteAffectAmino AcidsAnimal ModelAntioxidantsApoptoticArginineAttenuatedBase PairingBindingBiological AssayBreathingCandidate Disease GeneCardiovascular DiseasesCause of DeathCellsChronic Obstructive Airway DiseaseCigaretteCodeConfocal MicroscopyCytosineDataDevelopmentDiagnostic testsElementsEpithelialEpitheliumExcisionExtracellular FluidExtracellular MatrixExtracellular SpaceFunctional RNAGene ProteinsGenesGenetic PolymorphismGenetic Predisposition to DiseaseGenetic VariationGlycineGoalsGuanineHereditary DiseaseHeritabilityHumanHuman GeneticsIn VitroInflammationInjuryKnock-in MouseKnock-outKnockout MiceKnowledgeLaboratoriesLeadLength of StayLipopolysaccharidesLiquid substanceLungLung diseasesMacrophage ActivationMass Spectrum AnalysisMethodsMusMyocardial InfarctionNitric OxideObservational StudyOrganOxidantsOxidative StressPlasmaPopulationPredispositionProtein BindingProteinsPulmonary EmphysemaPulmonary Function Test/Forced Expiratory Volume 1ReportingResolutionResourcesRespiratory physiologyRiskRisk FactorsRoleSignal PathwaySingle Nucleotide PolymorphismSmokeSmokerSmokingStrokeStructure of parenchyma of lungSuperoxide DismutaseTestingTimeTissuesTobacco smokeToxinUnited StatesVariantWestern Blottingantioxidant therapybiobankcigarette smokingcytokineexperienceextracellulargenetic varianthuman DNAin vivolung injurymacrophagenovel diagnosticsoverexpressionpreventprotein distributionprotein functionresearch studyresponse
中文摘要
描述(由申请人提供):rs 1799895单核苷酸多态性(SNP)是SOD 3中的一种非同义碱基对变化,导致细胞外超氧化物歧化酶蛋白(EC-SOD)中的甘氨酸取代(R213 G)。该区域负责EC-SOD与细胞外基质的结合,使血浆水平增加10倍。R213 G SNP保护吸烟者免于发展慢性阻塞性肺疾病(COPD)和COPD急性加重。该提案的目的是阐明R213 G保护肺部免受烟草烟雾影响的机制。为了实现这一目标,我们创造了具有相同SNP的敲入小鼠。我们的方法将利用十多年研究EC-SOD基因和COPD的经验。
公共卫生相关性:慢性阻塞性肺疾病(COPD)是美国第四大常见死因。主要的风险因素是吸烟;然而,大多数吸烟者不会患上COPD。虽然COPD被认为是一种遗传性疾病,但只有少数基因变异与COPD反复相关。这些变异之一,细胞外超氧化物歧化酶基因(SOD 3)中的R213 G单核苷酸多态性,保护吸烟者免受COPD和COPD恶化。本研究将探讨R213 G保护肺免受哮喘诱导的肺损伤的机制。这些知识可能有助于开发新的诊断测试和治疗方法来预防和治疗COPD。
英文摘要
DESCRIPTION (provided by applicant): The rs1799895 single nucleotide polymorphism (SNP) is a non-synonymous base pair change in SOD3 that results in an arginine-to-glycine substitution (R213G) in extracellular superoxide dismutase protein (EC-SOD). This region is responsible for EC- SODs binding to extracellular matrix increases plasma levels 10-fold. The R213G SNP protects smokers from developing chronic obstructive pulmonary disease (COPD) and acute exacerbations of COPD. The goal of this proposal is to elucidate the mechanism by which the R213G protects the lung from tobacco smoke. To accomplish this aim, we have created a knock-in mouse with the identical SNP. Our methods will utilize more than a decade of experience studying the EC-SOD gene and COPD.
PUBLIC HEALTH RELEVANCE: Chronic obstructive pulmonary disease (COPD) is the fourth most common cause of death in the United States. The major risk factor is smoking; however, most smokers do not develop COPD. Although COPD is thought to be a genetic disease, there are only a few gene variants that have been repeatedly associated with COPD. One of these variants, the R213G single nucleotide polymorphism in the extracellular superoxide dismutase gene (SOD3), protects smokers from COPD and COPD exacerbations. This study will investigate the mechanisms by which R213G protects the lungs from cigarette-induced lung injury. This knowledge may help develop novel diagnostic tests and therapies to prevent and treat COPD.
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会议论文
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海外基金