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Protection of Intestine by the Bile Acid Receptor FXR

Protection of Intestine by the Bile Acid Receptor FXR
胆汁酸受体 FXR 对肠道的保护
批准号:
7013657
负责人:
STEVEN A. KLIEWER
金额:
$26.81万
依托单位国家:
美国
项目类别:
财政年份:
2004
资助国家:
美国
项目状态:
已结题
起止时间:
2004-03-01 至 2009-02-28

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中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The nuclear hormone receptors comprise a superfamily of ligand-activated transcription factors that regulate crucial aspects of human physiology. The study of these receptors has led to the identification of many unexpected and medically-important signaling pathways. Among the erstwhile "orphan" nuclear receptors for which physiological ligands have been discovered is the farnesoid X receptor (FXR), which is activated by bile acids. FXR is expressed in liver, where it regulates a program of genes involved in bile acid and lipid homeostasis. FXR is also highly expressed along the length of the small and large intestine; however, its function in the intestine is poorly understood. In this proposal, we hypothesize that FXR and its target gene, fibroblast growth factor (FGF)- 15, are components of a biological signal cascade that protects the mucosal layer of the intestine from the strong detergent effects of bile acids. This hypothesis is based on the following data: (i) FXR is strongly expressed in the villus epithelium and crypts; (ii) FXR-KO mice have a pronounced phenotype in the small intestine that includes blunted and dysmorphic villi and decreased number and/or size of mucus-secreting goblet cells; and, (iii) FXR dramatically induces expression of fibroblast growth factor (FGF)-15 in the villus epithelium of the small intestine. In Specific Aim 1, we will determine in which intestinal cell types FXR is expressed and whether it protects the intestine against chemical damage in vivo. In Specific Aim 2, we will characterize the expression pattern and actions of FGF-15 in the intestine and determine whether it is enteroprotective in vivo. In Specific Aim 3, the actions of FXR and FGF-15 on proliferation, apoptosis and intracellular signaling pathways will be studied in intestinal cell lines. This research will provide fundamental insights into the biology of the intestine and may have important implications for the treatment of inflammatory bowel diseases and other pathologic conditions that affect the intestinal mucosa.
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Coordinate Regulation of an Alcohol Protective Response by the Liver-derived Hormone FGF21
  • 批准号:
    10029530
  • 项目类别:
  • 资助金额:
    $36.78万
  • 财政年份:
    2020
  • 负责人:
    STEVEN A. KLIEWER
  • 依托单位:
Coordinate Regulation of an Alcohol Protective Response by the Liver-derived Hormone FGF21
  • 批准号:
    10453571
  • 项目类别:
  • 资助金额:
    $36.9万
  • 财政年份:
    2020
  • 负责人:
    STEVEN A. KLIEWER
  • 依托单位:
Coordinate Regulation of an Alcohol Protective Response by the Liver-derived Hormone FGF21
  • 批准号:
    10674919
  • 项目类别:
  • 资助金额:
    $36.9万
  • 财政年份:
    2020
  • 负责人:
    STEVEN A. KLIEWER
  • 依托单位:
The PPARgamma-FGF21 Signaling Pathway: Its Role in Thiazolidinedione Drug Action
  • 批准号:
    8074147
  • 项目类别:
  • 资助金额:
    $23.78万
  • 财政年份:
    2010
  • 负责人:
    STEVEN A. KLIEWER
  • 依托单位:
国内基金
海外基金
“肠—肝轴”PPARα/CYP8B1胆汁酸合成信号通路在减重手术改善糖脂代谢中的作用与机制
  • 批准号:
    82370902
  • 项目类别:
    面上项目
  • 资助金额:
    49.00万元
  • 批准年份:
    2023
  • 负责人:
    田景琰
  • 依托单位:
以胆酸为载体的肝靶向阿德福韦前体药物的研究