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Modulation of phenotypic and functional maturation of dendritic cells by intestinal bacteria and gliadin: relevance for celiac disease

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    SYSNO ASEP0387751
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleModulation of phenotypic and functional maturation of dendritic cells by intestinal bacteria and gliadin: relevance for celiac disease
    Author(s) De Palma, G. (ES)
    Kamanová, Jana (MBU-M) ORCID, RID
    Cinová, Jana (MBU-M)
    Olivares, M. (ES)
    Drašarová, Hana (MBU-M) RID
    Tučková, Ludmila (MBU-M) RID
    Sanz, Y. (ES)
    Source TitleJournal of Leukocyte Biology. - : Wiley - ISSN 0741-5400
    Roč. 92, č. 5 (2012), s. 1043-1054
    Number of pages12 s.
    Languageeng - English
    CountryUS - United States
    Keywordsbifidobacteria ; enterobacteria ; cell index
    Subject RIVEC - Immunology
    R&D ProjectsIAA500200801 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    GA310/07/0414 GA ČR - Czech Science Foundation (CSF)
    GD310/08/H077 GA ČR - Czech Science Foundation (CSF)
    GA310/09/1640 GA ČR - Czech Science Foundation (CSF)
    2B06155 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    Institutional supportMBU-M - RVO:61388971
    UT WOS000310584500015
    DOI10.1189/jlb.111581
    AnnotationDC maturation and functions are influenced by microbial and environmental stimuli, which could contribute to immune dysfunction. Here, we have investigated the role of enterobacteria ( Escherichia coli CBL2 and Shigella CBD8) isolated from CD patients, bifidobacteria ( Bifidobacterium longum CECT 7347 and Bifidobacterium bifidum CECT 7365), and gliadins on phenotypic and functional features of MDDCs and in coculture with Caco-2 cells. The ultimate goal of our study is to understand the roles played by specific components of the gut microbiota in CD. Enterobacteria induced marked alterations in MDDC morphology, inducing podosome dissolution and dendrites, and activated MDDC adhesion and spreading. Enterobacteria also induced inflammatory cytokine production (IFN-gamma, TNF-alpha, and IL-12), partially resembling the gliadin-induced Th1-type cytokine profile. B. longum CECT 7347 and B. bifidum CECT 7365 induced minor MDDC morphological changes and activated adhesion and spreading and inflammatory cytokine production to a lesser extent compared with enterobacteria. B. longum CECT 7347 also induced lower CD86 and CD40 expression on MDDCs than the two enterobacteria. The aforementioned bifidobacterial strain also reduced gliadin-induced IFN-gamma production and increased IL-10 secretion when both stimuli were combined. Similar trends were detected for MDDCs cocultured with Caco-2 cells. B. longum CECT 7347 reversed the gliadin-reduced ZO-1 expression in Caco-2 cells. Thus, our results suggest that specific components of the gut microbiota may influence phenotypic and functional maturation of DCs differently and their interactions with epithelial cells. This could ultimately define the role of DCs in CD progression
    WorkplaceInstitute of Microbiology
    ContactEliška Spurná, eliska.spurna@biomed.cas.cz, Tel.: 241 062 231
    Year of Publishing2013
Number of the records: 1  

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