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Role of the chloride channel ClC-2 in intestinal tight junction barrier recovery

氯离子通道 ClC-2 在肠道紧密连接屏障恢复中的作用

基本信息

批准号：
9755739
负责人：
Prashant Nighot
金额：
$ 8.16万
依托单位：
PENNSYLVANIA STATE UNIV HERSHEY MED CTR
依托单位国家：
美国
项目类别：
财政年份：
2014
资助国家：
美国
起止时间：
2014-04-01 至 2020-03-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/9755739
关键词：
Address Animal Model Antigens Apical Applications Grants CLC-2 protein Caveolae Cell Culture Techniques Clinical Colitis Complex Data Epithelial Epithelial Cells Epithelium Event Functional disorder Gastrointestinal Diseases Impairment In Vitro Inflammatory Inflammatory Bowel Diseases Injury Intestinal Mucosa Intestines Ions Ischemia Lateral Mediating Membrane Methods Molecular Biology Monomeric GTP-Binding Proteins Mucous Membrane Pathologic Patients Penetration Permeability Play Process Proteins Recovery Regulation Role Scaffolding Protein Structure Testing Therapeutic Tight Junctions Tissues Transmembrane Transport Ulcerative Colitis Villous Villus base caveolin 1 cellular imaging in vivo inflammatory disease of the intestine insight intestinal epithelium novel occludin prevent public health relevance recruit repaired restoration success trafficking

项目摘要

DESCRIPTION (provided by applicant): The apically located inter-cellular tight junctions (TJ) within the intestinal epithelium act as a paracellular barrier and prevent permeation of noxious luminal antigens. Loss of TJ barrier function is a key pathologic factor in intestinal disorders an inflammatory bowel diseases. Emerging evidence shows that intracellular vesicular membrane transport including caveolar transport is a key process in the formation of tight junction domains. Our preliminary studies indicated that the intestinal barrier recovery in the event of epithelial injury is impaired in the absence of ClC-2 chloride channel protein. Our preliminary studies also suggested that ClC-2 plays a vital role in the intestinal barrier recovery by modulation of intracellular trafficking of key tight junction protein occludin via its interaction with caveolae. Based on preliminary studies, we hypothesize that ClC-2 plays an integral role in the intestinal mucosal repair process by promoting recruitment of tight junction protein occludin via caveolin-1 dependent process. In specific aim 1, we plan to elucidate the role of ClC-2 in caveolar trafficking of occludin, and in aim 2, we intend to define the mechanisms of ClC-2 mediated enhancement of intestinal epithelial TJ barrier. Specific aim 3 is dedicated to testing our hypothesis in-vivo and defining the role of ClC-2 in intestinal barrier recovery. Clinically, repai of mucosal barrier in intestine is imperative for preventing further intestinal mucosal damage, and for therapeutic success. This study will provide a novel insight into the crucial role ClC-2 plays n intestinal barrier recovery. The proposed studies will provide us with mechanistic and potentially therapeutic information on how chloride channel ClC-2 enhances the gut barrier function.

描述（由申请人提供）：位于肠上皮顶端的细胞间紧密连接（TJ）作为细胞旁屏障，防止有害腔内抗原的渗透。TJ屏障功能的丧失是肠道疾病和炎症性肠病的关键病理因素。越来越多的证据表明，细胞内的囊泡膜运输包括小泡运输是紧密连接域形成的关键过程。