Role of the chloride channel ClC-2 in intestinal tight junction barrier recovery
Role of the chloride channel ClC-2 in intestinal tight junction barrier recovery
批准号:
9242021
负责人:
Prashant Nighot
金额:
$14.79万
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-04-01 至 2019-03-31
关键词:
AddressAnimal ModelAntigensApicalApplications GrantsCLC-2 proteinCaveolaeCell Culture TechniquesClinicalColitisComplexDataEpithelialEpithelial CellsEpitheliumEventFunctional disorderGastrointestinal DiseasesImpairmentIn VitroInflammatoryInflammatory Bowel DiseasesInflammatory disease of the intestineInjuryIntestinesIonsIschemiaLateralMediatingMembraneMethodsMolecular BiologyMonomeric GTP-Binding ProteinsPathologicPatientsPenetrationPermeabilityPlayProcessProteinsRecoveryRecruitment ActivityRegulationRoleScaffolding ProteinStructureTestingTherapeuticTight JunctionsTissuesTransmembrane TransportUlcerative ColitisVillousVillusbasecaveolin 1cellular imagingin vivoinsightintestinal epitheliumnoveloccludinpreventpublic health relevancerepairedrestorationsuccesstrafficking
中文摘要
描述(申请人提供):位于肠上皮顶端的细胞间紧密连接(TJ)起到细胞旁屏障的作用,阻止有害管腔抗原的渗透。TJ屏障功能的丧失是肠道疾病-炎症性肠病的关键病理因素。新的证据表明,细胞内的囊泡膜转运,包括空泡转运,是紧密连接结构域形成的关键过程。
我们的初步研究表明,在缺乏ClC-2氯通道蛋白的情况下,肠上皮损伤时肠屏障的恢复会受到损害。我们的初步研究还表明,ClC-2通过与小窝的相互作用来调节关键紧密连接蛋白occludin的细胞内转运,从而在肠屏障的恢复中发挥重要作用。
在初步研究的基础上,我们假设ClC-2通过小窝蛋白-1依赖的过程促进紧密连接蛋白occludin的募集,从而在肠粘膜修复过程中发挥不可或缺的作用。在特定的目标1中,我们计划阐明ClC-2在封闭素空泡运输中的作用,在目标2中,我们打算确定ClC-2介导的增强肠上皮TJ屏障的机制。具体目标3致力于在体内测试我们的假说,并确定ClC-2在肠道屏障恢复中的作用。临床上,肠粘膜屏障的修复对于预防进一步的肠粘膜损伤和治疗的成功是必不可少的。这项研究将为ClC-2在肠道屏障恢复中的关键作用提供新的见解。这些拟议的研究将为我们提供氯离子通道ClC-2如何增强肠道屏障功能的机制和潜在的治疗信息。
英文摘要
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.
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会议论文
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项目类别:
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资助金额:$14.79万
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财政年份:2014
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负责人:Prashant Nighot
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依托单位:
海外基金