THE ROLE OF ICSBP IN MUCOSAL IMMUNE RESPONSE
THE ROLE OF ICSBP IN MUCOSAL IMMUNE RESPONSE
批准号:
7484982
负责人:
HUABAO XIONG
金额:
$19.95万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-09-01 至 2011-08-31
关键词:
AgreementAntibodiesAutomobile DrivingBindingCellsChronicColitisColonControlled StudyCrohn&aposs diseaseDendritic CellsDevelopmentDiseaseDisruptionEnvironmentFamilyGene ExpressionGenerationsGenus ColaGerm-FreeGoalsHost DefenseHumanIFN consensus sequence binding proteinIL10 geneImmuneImmune responseImmunologicsIndividualInflammationInflammatoryInflammatory ResponseInflammatory disease of the intestineInterferonsInterleukin-10Interleukin-12Knockout MiceLamina PropriaLigandsMediatingMessenger RNAModelingMolecularMononuclearMucosal Immune ResponsesMucositisMusPathway interactionsPatientsPeptidesPlayProductionProteinsReagentRegulationReportingRoleSignal PathwaySignal TransductionSiteStructureSulfonic AcidsT-LymphocyteTLR4 geneTNF receptor-associated factor 6TRAF6 geneTherapeutic EffectToll-like receptorsTrinitrobenzenesUbiquitinUbiquitinationcytokinein vivomacrophagemicrobialmouse modelmulticatalytic endopeptidase complexpathogenpromotertherapeutic targettranscription factorubiquitin-protein ligase
中文摘要
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英文摘要
The IFN consensus sequence binding protein (ICSBP/IRF-8), which belongs to the interferon
regulatory factor family of transcription factors, is essential for a Thl immune response.
ICSBP plays an important role in the host defense against microbial pathogens, but the exact
roles of ICSBP in inflammation and chronic inflammatory diseases are still not clear. IL-10-/-
mice, which develop colitis characterized by increased Thl cytokines, mimic many aspects of
human Crohn's disease (CD). The importance of ICSBP in the development of colitis is shown
by the lack of disease in ICSBP and IL-10 double knockout mice. In addition, ICSBP mRNA
and protein are highly expressed in the colons of IL-10-/- mice with colitis, while expression
of IL-12 and iNOS is significantly compromised in ICSBP/IL-10 double KO mice. In agreement
with these results, patients with CD have significantly higher ICSBP expression than normal
individuals. ICSBP is active in several loci. ICSBP interacts with TRAF6 in the TLR4 pathway,
and binds to ISRE sites in the iNOS and IL-12 p40 promoters, activating the expression of
these genes. In addition, we find that ICSBP is ubiquitinated by the E3 ligase Cbl, resulting in
its degradation by the proteasome. To expore ICSBP as a suitable target for therapy in CD,
this proposal is structured around three aims: 1) We will analyze the regulation of ICSBP
expression in macrophages and dendritic cells activated with various TLR and NOD2 ligands.
In addition, we will define the role of ICSBP in the generation of regulatory T cells. 2) We will
define the function of Cbl in the control of Thl immune immune response and analyze the
role of Cbl in the development of colitis. 3) We will define the therapeutic effects of TLR4 and
ICSBP inhibition by cell-permeable peptide reagent in vivo in murine colitis models. These
studies will advance our understanding the role of ICSBP in the mucosal immune response,
and may identify ICSBP as a new target for therapy in CD.
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资助金额:$42.38万
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财政年份:--
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THE ROLE OF ICSBP IN MUCOSAL IMMUNE RESPONSE
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批准号:7683157
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资助金额:$20.21万
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依托单位:
THE ROLE OF ICSBP IN MUCOSAL IMMUNE RESPONSE
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批准号:7921633
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项目类别:
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资助金额:$21.99万
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财政年份:--
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负责人:HUABAO XIONG
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依托单位:
海外基金