Novel Effects of Gravity on Intestinal Epithelial Barrier Responses to Alcohol
Novel Effects of Gravity on Intestinal Epithelial Barrier Responses to Alcohol
批准号:
7942461
负责人:
Declan McCole
金额:
$22.33万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-09-01 至 2012-08-31
关键词:
3-DimensionalAcetaldehydeAddressAffectAlcohol consumptionAlcoholic Liver DiseasesAlcoholsApicalBacteriaBathingBehaviorBioreactorsCarbohydratesCause of DeathCell Culture SystemCell Culture TechniquesCell DeathCell LineCell modelCell surfaceCellsCenters for Disease Control and Prevention (U.S.)Cessation of lifeCollectionConsultationsCulture MediaCultured CellsD CellsDataDevelopmentDiffusionDimensionsDiseaseEndotoxinsEnvironmentEpithelialEpithelial CellsEventExhibitsExposure toFiberForce of GravityFormalinFunctional disorderGasesGelatinGrowthHealthHumanHuman bodyHypogravityImmune systemInjuryInternationalIntestinal ContentIntestinesInvestigationKnowledgeLaboratoriesLife StyleLipopolysaccharidesLiverMaintenanceMeasurementMeasuresMedicalMembraneMicrobeMicrogravityMicroscopyModelingMolecular TargetMonitorNutrientOrganPancreatitisPatientsPerfusionPermeabilityPhasePhosphorylationPhysiologicalPlayPost-Translational Protein ProcessingPrevention strategyProcessPropertyProteinsRegulationResistanceRoleScaffolding ProteinSeedsShapesSignaling MoleculeSimulateState of Zero GravityStructureSurfaceSystemTechnologyTemperatureTestingTight JunctionsTimeTissuesToxic ActionsToxinTubeUnited States National Aeronautics and Space AdministrationValidationVascular blood supplyWestern BlottingWidthalcohol abuse therapyalcohol effectalcohol responsealcohol use initiationbasecell fixationcell growthcellular microvilluschronic alcohol ingestiondensitydesignexperiencegastrointestinalgenetic regulatory proteinin vivoinsightintestinal epitheliummacromoleculemonolayerneuronal cell bodynovelnovel therapeuticsprogramsprotein expressionpublic health relevanceresearch studyresponsesolutethree dimensional structure
中文摘要
描述(申请人提供):酒精会增加胃肠道对细菌和细菌内毒素(内毒素)的通透性,这在酒精引起的组织/器官损伤,特别是酒精性肝病(ALD)的启动中起着主要作用。通透性增加似乎主要是通过有毒代谢物乙醛对形成肠屏障主要成分的上皮间紧密连接(TJ)的作用而发生的。因此,了解酒精促进肠上皮细胞(IEC)通透性的潜在机制对于制定预防或治疗酒精相关医学疾病的策略非常重要。在人体内,细胞通常生长在蛋白质和碳水化合物纤维的支架内,这些支架有助于创建三维(3D)结构,从而使器官保持其形状。在研究地球上的细胞时出现了困难,因为在体外,细胞往往生长在平板上,无法复制它们通常持有的结构。因此,三维微重力环境可能代表了体内更准确的上皮行为的细胞培养模型。此外,国际空间站上没有重力对上皮细胞屏障功能的基本物理作用力,这为研究重力对细胞特性的影响提供了一个独特的机会。我们假设,微重力对肠上皮细胞屏障特性的影响显著改变了酒精对上皮屏障功能的影响。我们将在UH2阶段通过(I)量化模拟微重力对肠上皮细胞紧密连接蛋白和上皮通透性的影响;(Ii)测试酒精对模拟微重力下IEC屏障特性的影响;(Iii)优化三维细胞培养系统,以研究国际空间站上的屏障功能。在UH3阶段,我们将(Iv)量化微重力对国际空间站上酒精诱导的IEC通透性的影响。这些研究将提供一个明确的答案,即重力在多大程度上影响上皮屏障功能,以及这如何影响上皮细胞对摄入毒素的反应。因此,我们将提供可能对人类健康产生重大积极影响的新的基础知识,并允许合理开发与饮酒和肠道屏障功能缺陷相关的疾病的新治疗策略。
与公共健康相关:从2001年到2005年,每年约有79,000人死于过度饮酒,这是美国每年与生活方式有关的第三大死因(疾病控制中心)。酒精引起的疾病的一个主要因素是酒精能够损害肠道上皮细胞的正常屏障功能。该项目将利用国际空间站(ISS)独特的零重力环境,对重力在调节肠道屏障特性中的作用以及重力缺失如何改变酒精对肠道上皮细胞屏障功能的有害影响产生新的基本见解。
英文摘要
DESCRIPTION (provided by applicant): Alcohol administration increases gastrointestinal permeability to bacteria and bacterial endotoxin (lipopolysaccharide (LPS)), and this plays a major role in the initiation of alcohol-induced tissue/organ damage in particular, alcoholic liver disease (ALD). Increased permeability appears to occur principally though the action of the toxic metabolite, acetaldehyde, on interepithelial tight junctions (TJ) that form a major component of the intestinal barrier. Therefore, understanding the underlying mechanisms by which alcohol promotes intestinal epithelial cell (IEC) permeability is important in designing strategies for the prevention or treatment of alcohol-associated medical disorders. In the human body, cells normally grow within a scaffolding of protein and carbohydrate fibers that help create a three dimensional (3-D) structure, thus allowing organs maintain their shape. Difficulties arise when studying cells on Earth as outside of the body, cells tend to grow in flat sheets and are not capable of duplicating the structure they normally hold. Therefore, a 3-D microgravity environment likely represents a more accurate cell culture model of epithelial behavior in vivo. Furthermore, the absence of the fundamental physical force of gravity on epithelial cell barrier function on board the ISS lends a unique opportunity to study the influence of gravity on cellular properties. We hypothesize that the influence of microgravity on the barrier properties of intestinal epithelial cells significantly modifies alcohol-induced effects on epithelial barrier function. We will test this hypothesis in the UH2 phase by (i) quantifying the effects of simulated microgravity on intestinal epithelial cell tight junction proteins and epithelial permeability; (ii) testing the effects of alcohol on barrier properties of IEC under simulated microgravity; (iii) optimizing a 3-dimensional cell culture system to study barrier function on board the ISS. In the UH3 phase we will (iv) quantify the effects of microgravity on IEC permeability induced by alcohol on board the ISS. These studies will provide a definitive answer as to what extent epithelial barrier function is influenced by gravity, and how this impacts upon epithelial responses to ingested toxins. As a result, we will provide new and fundamental knowledge that will likely have significant positive effects on human health, and allow the rational development of new therapeutic strategies for diseases associated with alcohol consumption and deficient intestinal barrier function.
PUBLIC HEALTH RELEVANCE: From 2001-2005, there were approximately 79,000 deaths annually attributable to excessive alcohol use, the 3rd leading lifestyle-related cause of death for people in the U.S. each year (Centers for Disease Control). A major contributor to alcohol-induced disease is the ability of alcohol to compromise the normal barrier function of intestinal epithelial cells that line the gut. This project will utilize the unique zero- gravity environment of the International Space Station (ISS) to generate novel fundamental insights into the role of gravity in regulating intestinal barrier properties, and how the absence of gravity modifies the detrimental influence of alcohol on intestinal epithelial cell barrier function.
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