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Disruption of E-cadherin-mediated adhesion induces a functionally distinct pathway of dendritic cell maturation.

Disruption of E-cadherin-mediated adhesion induces a functionally distinct pathway of dendritic cell maturation. Research Abstract Details 

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  • Disruption of E-cadherin-mediated adhesion induces a functionally distinct pathway of dendritic cell maturation. Abstract Text:

    aimin jiangAimin Jiang,ona bloomOna Bloom,satoru onoSatoru Ono,weiguo cuiWeiguo Cui,juli unternaehrerJuli Unternaehrer,shan jiangShan Jiang,j andrew whitneyJ Andrew Whitney,john connollyJohn Connolly,jacques banchereauJacques Banchereau,ira mellmanIra Mellman,aimin jiangAimin Jiang,ona bloomOna Bloom,satoru onoSatoru Ono,weiguo cuiWeiguo Cui,juli unternaehrerJuli Unternaehrer,shan jiangShan Jiang,j andrew whitneyJ Andrew Whitney,john connollyJohn Connolly,jacques banchereauJacques Banchereau,ira mellmanIra Mellman,

    The maturation of dendritic cells (DCs) after exposure to microbial products or inflammatory mediators plays a critical role in initiating the immune response. We found that maturation can also occur under steady-state conditions, triggered by alterations in E-cadherin-mediated DC-DC adhesion. Selective disruption of these interactions induced the typical features of DC maturation including the upregulation of costimulatory molecules, MHC class II, and chemokine receptors. These events were triggered at least in part by activation of the beta-catenin pathway. However, unlike maturation induced by microbial products, E-cadherin-stimulated DCs failed to release immunostimulatory cytokines, exhibiting an entirely different transcriptional profile. As a result, E-cadherin-stimulated DCs elicited an entirely different T cell response in vivo, generating T cells with a regulatory as opposed to an effector phenotype. These DCs induced tolerance in vivo and may thus contribute to the elusive steady-state "tolerogenic DCs."

    Disruption of E-cadherin-mediated adhesion induces a functionally distinct pathway of dendritic cell maturation. Publishing Authors By Initials

    a jiangA Jiang,o bloomO Bloom,s onoS Ono,w cuiW Cui,j unternaehrerJ Unternaehrer,s jiangS Jiang,ja whitneyJA Whitney,j connollyJ Connolly,j banchereauJ Banchereau,i mellmanI Mellman,a jiangA Jiang,o bloomO Bloom,s onoS Ono,w cuiW Cui,j unternaehrerJ Unternaehrer,s jiangS Jiang,ja whitneyJA Whitney,j connollyJ Connolly,j banchereauJ Banchereau,i mellmanI Mellman,

    For similar abstracts research abstracts see: abstracts research

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    Disruption of E-cadherin-mediated adhesion induces a functionally distinct pathway of dendritic cell maturation. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Immunity

    VOLUME: 27

    Page Numbers: 610-24

    Journal Abbreviation: Immunity

    ISSN: 1074-7613

    DAY: 11

    MONTH: 10

    YEAR: 2007

    Disruption of E-cadherin-mediated adhesion induces a functionally distinct pathway of dendritic cell maturation. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9432918

    Disruption of E-cadherin-mediated adhesion induces a functionally distinct pathway of dendritic cell maturation. Keywords Mesh Terms:

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    Grant and Affiliation Information for Disruption of E-cadherin-mediated adhesion induces a functionally distinct pathway of dendritic cell maturation.

    AFFILIATION: Department of Cell Biology, Ludwig Institute for Cancer Research, Yale University School of Medicine, 333 Cedar Street, PO Box 208002, New Haven, CT 06520, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIAID

    GRANT: U19AI057234

    ACRONYM: AI

    MEDLINETA: Immunity

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