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中文摘要
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描述(由申请方提供):上皮紧密连接完整性的建立和维持对上皮器官的正常功能至关重要;最重要的是,肠上皮在吸收营养物质的同时作为抗原和病原体的选择性屏障的能力是肠功能的基础。此外,紧密连接以及相关的极性复合物对于维持上皮极性至关重要。我们对上皮细胞的发育和极性的研究主要集中在内体蛋白,内管蛋白。内管蛋白是一种存在于极化上皮细胞顶端内体的膜蛋白。它在发育中的肠中以高水平表达,特别是当肠细胞建立极性时。此外,内管蛋白可能通过与aPKC和Rab 14相互作用调节连接完整性和上皮极性。在这个建议中,我们将阐明的作用机制,内皮素和Rab 14在建立和维持上皮紧密连接和极性。本提案中概述的实验将定义内管蛋白和Rab 14在靶向连接和顶端蛋白中的作用,并阐明内管蛋白对上皮连接的建立和维持至关重要的基序。我们的假设是,内管蛋白作为一个支架蛋白组织和目标的连接和极性蛋白从顶端内体。内管蛋白功能的丧失可能导致屏障功能和/或顶-基底外侧极性的丧失,导致新生儿免疫力受损,增加对炎症性肠病和/或癌症的易感性。
英文摘要
DESCRIPTION (provided by applicant): The establishment and maintenance of epithelial tight junction integrity is essential to the normal function of epithelial organs; above all, the ability of the intestinal epithelium to serve as a selective barrier to antigens and pathogens while absorbing nutrients is fundamental to intestinal function. Also, tight junctions together with associated polarity complexes are critical for the maintenance of epithelial polarity. Our investigations of epithelial development and polarity have focused on the endosomal protein, endotubin. Endotubin is an integral membrane protein that is resident in apical endosomes of polarized epithelial cells. It is expressed at high levels in developing intestine, particularly when the enterocytes are establishing polarity. Moreover, endotubin regulates junctional integrity and epithelial polarity, possibly through interaction with aPKC and Rab14. In this proposal, we will elucidate the mechanism of action of endotubin and Rab14 in the establishment and maintenance of epithelial tight junctions and polarity. Experiments outlined in this proposal will define the role of endotubin and Rab14 in targeting of junctional and apical proteins and elucidate the motifs of endotubin critical for the establishment and maintenance of epithelial junctions. Our hypothesis is that endotubin serves as a scaffolding protein to organize and target junctional and polarity proteins from the apical endosomes. Loss of endotubin function could result in loss of barrier function and/or apical-basolateral polarity, leading to compromised immunity in the newborn, increased susceptibility to inflammatory bowel disease, and/or cancer.
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Autophagy and LC3-associated phagocytosis in intestinal epithelial cells
  • 批准号:
    10538801
  • 项目类别:
  • 资助金额:
    $45.09万
  • 财政年份:
    2022
  • 负责人:
    Jean M Wilson
  • 依托单位:
Autophagy and LC3-associated phagocytosis in intestinal epithelial cells
  • 批准号:
    10671568
  • 项目类别:
  • 资助金额:
    $45.09万
  • 财政年份:
    2022
  • 负责人:
    Jean M Wilson
  • 依托单位:
Endocytic Regulation of Intestinal Development
  • 批准号:
    9262626
  • 项目类别:
  • 资助金额:
    $41.47万
  • 财政年份:
    2017
  • 负责人:
    Jean M Wilson
  • 依托单位:
Regulation of Intestinal Tight Junction Structure by Membrane Traffic
  • 批准号:
    8212059
  • 项目类别:
  • 资助金额:
    $32.95万
  • 财政年份:
    2011
  • 负责人:
    Jean M Wilson
  • 依托单位:
国内基金
海外基金
Neo-antigens暴露对肾移植术后体液性排斥反应的影响及其机制研究
  • 批准号:
    2022J011295
  • 项目类别:
    省市级项目
  • 资助金额:
    10.0万元
  • 批准年份:
    2022
  • 负责人:
    王亚伟
  • 依托单位:
结核分枝杆菌持续感染期抗原(latency antigens)的重组BCG疫苗研究