Number of the records: 1  

Gliadin fragments promote migration of dendritic cells

  1. 1.
    SYSNO ASEP0361617
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleGliadin fragments promote migration of dendritic cells
    Author(s) Chládková, Barbara (MBU-M) RID
    Kamanová, Jana (MBU-M) ORCID, RID
    Palová-Jelínková, Lenka (MBU-M) RID
    Cinová, Jana (MBU-M)
    Šebo, Peter (MBU-M) RID, ORCID
    Tučková, Ludmila (MBU-M) RID
    Source TitleJournal of Cellular and Molecular Medicine. - : Wiley - ISSN 1582-1838
    Roč. 15, č. 4 (2011), 938-948
    Number of pages11 s.
    Languageeng - English
    CountryUS - United States
    Keywordsceliac disease ; gliadin ; dendritic cell
    Subject RIVEC - Immunology
    R&D ProjectsGA310/07/0414 GA ČR - Czech Science Foundation (CSF)
    GD310/08/H077 GA ČR - Czech Science Foundation (CSF)
    GA310/08/0447 GA ČR - Czech Science Foundation (CSF)
    IAA500200801 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    IAA500200914 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    CEZAV0Z50200510 - MBU-M (2005-2011)
    UT WOS000290312700019
    DOI10.1111/j.1582-4934.2010.01066.x
    AnnotationThis study provides a new insight into pathogenic features of gliadin fragments by demonstrating their ability to promote DC migration, which is a prerequisite for efficient priming of naive T cells, contributing to celiac disease pathology. In genetically predisposed individuals, ingestion of wheat gliadin provokes a T-cell-mediated enteropathy, celiac disease. Gliadin fragments were previously reported to induce phenotypic maturation and Th1 cytokine production by human dendritic cells (DCs) and to boost their capacity to stimulate allogeneic T cells. Here, we monitor the effects of gliadin on migratory capacities of DCs. Using transwell assays, we show that gliadin peptic digest stimulates migration of human DCs and their chemotactic responsiveness to the lymph node-homing chemokines CCL19 and CCL21
    WorkplaceInstitute of Microbiology
    ContactEliška Spurná, eliska.spurna@biomed.cas.cz, Tel.: 241 062 231
    Year of Publishing2012
Number of the records: 1  

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