Molecular Control of Gut Permeability in Trauma
Molecular Control of Gut Permeability in Trauma
批准号:
10663173
负责人:
MACK H WU
金额:
$0.0万
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:
2010-04-01 至 2023-12-31
关键词:
AccidentsAllergensAmerican soldierAnimalsBacterial TranslocationCellsCellular biologyChemical BurnsCirculationClinicalClinical ResearchCoupledCritical CareDataDevelopmentDiffusionDiseaseEndotheliumEpithelial AttachmentEpitheliumEvaluationExperimental DesignsFailureFire - disastersFocal Adhesion Kinase 1Focal AdhesionsFunctional disorderGeneticGoalsGut MucosaImageImmune System DiseasesImpairmentIn VitroIncidenceInflammationInflammatoryInflammatory ResponseInjuryIntercellular JunctionsInterventionIntestinal MucosaIntestinal permeabilityIntestinesIschemiaKnowledgeLeaky GutLength of StayLeukocytesLifeLinkLymphMediatingMediationMedicalMesenteryMicrocirculationModificationMolecularMorbidity - disease rateMucositisMucous MembraneMultiple Organ FailureNeutrophil InfiltrationOperative Surgical ProceduresOrganPathogenesisPathway interactionsPatientsPermeabilityPhosphotransferasesPhysiologicalPlayPropertyProtein Tyrosine KinaseProteinsRegulationResearchResearch DesignRoleSepsisSeveritiesSiteSyndromeTestingTherapeuticTight JunctionsTimeTissuesToxinTraumaTrauma patientVeteransWorkclinically relevantcombateffective therapyexperimental studygastrointestinalgastrointestinal epitheliumgenetic approachheat injuryimprovedin vitro Modelin vivoin vivo Modelinnovationintestinal barrierintravital microscopymortalitymouse modelnew therapeutic targetnovelorgan injurypharmacologicresponseseptic patientssevere burnssevere injurysolutesystemic inflammatory responsewound treatment
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Project Summary
Systemic inflammation and multiple organ failure associated with trauma are a major cause of
mortality and morbidity in American soldiers and veterans. Intestinal barrier dysfunction plays
an important role in the development of posttraumatic complications such as sepsis by
providing the major site for diffusion of toxins, allergens and bacterial translocation to the
circulation. Despite the well- recognized importance of gut dysfunction in the pathogenesis of
posttraumatic complications, the intestinal permeability response to severe burns, a major form
of trauma, has not been well characterized, and its cellular and molecular mechanisms have
not been fully understood. The goal of this study is to elucidate the cell-specific mechanisms of
leaky guts during thermal injury. The hypothesis to be tested is that thermal injury induced
inflammation in gut tissue activates focal adhesion kinase (FAK) activity in gut epithelium,
stimulates focal remodeling and epithelial junction disassociation, therefore impairing gut
epithelial barrier integrity. Two specific aims are developed in this proposal to: 1) characterize
functional role of FAK mediated intestinal barrier dysfunction and therapeutic potential of FAK
inhibition during thermal injury, and 2) explore the molecular mechanism of FAK mediated gut
epithelial barrier dysfunction. The study design employs complimentary in vivo, ex vivo, and in
vitro models that incorporate molecular and genetic approaches into physiological experiments
under clinically relevant trauma conditions. The significance of the study lies in its potential to
establish a new molecular mechanism in the regulation of gut epithelial barrier function. The data
derived from this project will enhance our understanding of pathophysiological mechanisms
involved in gut epithelial barrier function. More importantly, it will expand our knowledge of
gastrointestinal pathobiology and contribute to the development of effective therapies and
surgical interventions against gut barrier injury in patients suffered from trauma or inflammatory
diseases.
期刊论文(10)
专著(0)
科研奖励(0)
会议论文
登录
查看更多内容
DOI:
10.1371/journal.pone.0154351
发表时间:
2016
期刊:
PloS one
影响因子:
3.7
作者:
[Haines RJ, Beard RS Jr, Eitner RA, Chen L, Wu MH]
通讯作者:
Wu MH
DOI:
10.3389/fimmu.2020.586685
发表时间:
2020
期刊:
Frontiers in immunology
影响因子:
7.3
作者:
[Ma Y, Zabell T, Creasy A, Yang X, Chatterjee V, Villalba N, Kistler EB, Wu MH, Yuan SY]
通讯作者:
Yuan SY
DOI:
10.1097/shk.0b013e318268c731
发表时间:
2012-10
期刊:
Shock (Augusta, Ga.)
影响因子:
--
作者:
[Guo M, Yuan SY, Frederich BJ, Sun C, Shen Q, McLean DL, Wu MH]
通讯作者:
Wu MH
DOI:
10.1007/s10620-016-4145-y
发表时间:
2016-08
期刊:
Digestive diseases and sciences
影响因子:
3.1
作者:
[Haines RJ, Beard RS Jr, Chen L, Eitnier RA, Wu MH]
通讯作者:
Wu MH
DOI:
10.1161/jaha.116.003336
发表时间:
2016-04-05
期刊:
Journal of the American Heart Association
影响因子:
5.4
作者:
[Breslin JW, Daines DA, Doggett TM, Kurtz KH, Souza-Smith FM, Zhang XE, Wu MH, Yuan SY]
通讯作者:
Yuan SY
共 6 条
Extracellular Histones in Burn-induced Microvascular Hyperpermeability
-
批准号:10609034
-
项目类别:
-
资助金额:$31.17万
-
财政年份:2022
-
负责人:MACK H WU
-
依托单位:
Extracellular Histones in Burn-induced Microvascular Hyperpermeability
-
批准号:10443933
-
项目类别:
-
资助金额:$31.1万
-
财政年份:2022
-
负责人:MACK H WU
-
依托单位:
Endothelial glycocalyx shedding in septic injury
-
批准号:10374295
-
项目类别:
-
资助金额:$47.07万
-
财政年份:2021
-
负责人:MACK H WU
-
依托单位:
Endothelial glycocalyx shedding in septic injury
-
批准号:10532364
-
项目类别:
-
资助金额:$46.58万
-
财政年份:2021
-
负责人:MACK H WU
-
依托单位:
BLRD Research Career Scientist Award Application
-
批准号:9899092
-
项目类别:
-
资助金额:$0.0万
-
财政年份:2018
-
负责人:MACK H WU
-
依托单位:
BLRD Research Career Scientist Award Application
-
批准号:10693575
-
项目类别:
-
资助金额:$0.0万
-
财政年份:2018
-
负责人:MACK H WU
-
依托单位:
BLRD Research Career Scientist Award Application
-
批准号:9553000
-
项目类别:
-
资助金额:$0.0万
-
财政年份:2018
-
负责人:MACK H WU
-
依托单位:
BLRD Research Career Scientist Award Application
-
批准号:10265422
-
项目类别:
-
资助金额:$0.0万
-
财政年份:2018
-
负责人:MACK H WU
-
依托单位:
BLRD Research Career Scientist Award Application
-
批准号:10454207
-
项目类别:
-
资助金额:$0.0万
-
财政年份:2018
-
负责人:MACK H WU
-
依托单位:
Endothelial focal adhesions in microvascular barrier dysfunction during ischemia-
-
批准号:8767044
-
项目类别:
-
资助金额:$37.38万
-
财政年份:2014
-
负责人:MACK H WU
-
依托单位:
Endothelial focal adhesions in microvascular barrier dysfunction during ischemia-
-
批准号:9276101
-
项目类别:
-
资助金额:$37.38万
-
财政年份:2014
-
负责人:MACK H WU
-
依托单位:
Endothelial focal adhesions in microvascular barrier dysfunction during ischemia-
-
批准号:8900330
-
项目类别:
-
资助金额:$36.81万
-
财政年份:2014
-
负责人:MACK H WU
-
依托单位:
Endothelial focal adhesions in microvascular barrier dysfunction during ischemia-
-
批准号:9099933
-
项目类别:
-
资助金额:$37.38万
-
财政年份:2014
-
负责人:MACK H WU
-
依托单位:
Molecular Control of Gut Permeability in Trauma
-
批准号:7932507
-
项目类别:
-
资助金额:$0.0万
-
财政年份:2010
-
负责人:MACK H WU
-
依托单位:
Molecular Control of Gut Permeability in Trauma
-
批准号:10084211
-
项目类别:
-
资助金额:$0.0万
-
财政年份:2010
-
负责人:MACK H WU
-
依托单位:
Molecular Control of Gut Permeability in Trauma
-
批准号:8259082
-
项目类别:
-
资助金额:$0.0万
-
财政年份:2010
-
负责人:MACK H WU
-
依托单位:
Molecular Control of Gut Permeability in Trauma
-
批准号:8397572
-
项目类别:
-
资助金额:$0.0万
-
财政年份:2010
-
负责人:MACK H WU
-
依托单位:
Molecular Control of Gut Permeability in Trauma
-
批准号:8734716
-
项目类别:
-
资助金额:$0.0万
-
财政年份:2010
-
负责人:MACK H WU
-
依托单位:
Molecular Control of Gut Permeability in Trauma
-
批准号:8195838
-
项目类别:
-
资助金额:$0.0万
-
财政年份:2010
-
负责人:MACK H WU
-
依托单位:
Microvascular Permeability and Matrix Fibrinogen Degradation in Trauma
-
批准号:7696289
-
项目类别:
-
资助金额:$38.25万
-
财政年份:2009
-
负责人:MACK H WU
-
依托单位:
海外基金