The role of Foxo1 for intestinal epithelial cells during mucosal immune response
The role of Foxo1 for intestinal epithelial cells during mucosal immune response
批准号:
10262436
负责人:
Chuan Wu
金额:
$54.37万
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至
关键词:
Cell CommunicationCell physiologyCellsCytoplasmDataDendritic CellsEnvironmentEpithelial CellsEquilibriumExhibitsFOXO1A geneFOXP3 geneGoblet CellsHuman GeneticsImmuneImmune ToleranceImmune responseImmunologyImpairmentInflammatory Bowel DiseasesIntestinesMediatingMolecularMucinsMucosal Immune ResponsesMucous body substanceMusPathway interactionsPlayPredispositionProteinsRegulatory T-LymphocyteResearchRoleT cell responseT-LymphocyteTestingbaseeffector T cellgenetic linkagegenome wide association studygut microbeshigh riskinflammatory disease of the intestineintestinal epitheliumtranscription factor
中文摘要
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英文摘要
It is known that intestinal epithelial cells (IECs) interact with immune cells to modulate intestinal or systemic immune responses. Dendritic cells (DCs) are one crucial component in maintaining intestinal immune tolerance. However, how IECs and DCs collaborate to maintain the gut immune balance is still unclear. We further found that one transcription factor Foxo1, plays a critical role for IECs function. The loss of Foxo1 within IECs leads to altered mucus layer formation and DCs function. Consequently, mice without Foxo1 in IECs exhibit enhanced susceptibility to intestinal inflammation. We have hypothesized that IEC-derived Foxo1 regulates the IEC-DC interaction for intestinal tolerance via mucin protein. We are currently studying the cellular and molecular mechanisms of how Foxo1 regulates IECs interaction with DCs.
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海外基金