课题基金 / 基金详情

Molecular Control of Gut Permeability in Trauma

Molecular Control of Gut Permeability in Trauma
创伤中肠道通透性的分子控制
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

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中文摘要
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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)
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会议论文
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
6
    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:
    海外基金