Počet záznamů: 1  

Epigenetic changes at Il12rb2 and Tbx21 in relation to plasticity behavior of Th17 cells

  1. 1.
    SYSNO ASEP0375132
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevEpigenetic changes at Il12rb2 and Tbx21 in relation to plasticity behavior of Th17 cells
    Tvůrce(i) Bending, D. (GB)
    Newland, S. (GB)
    Krejčí, Alena (BC-A) RID, ORCID
    Phillips, J. M. (GB)
    Bray, S. (GB)
    Cooke, A. (GB)
    Celkový počet autorů6
    Zdroj.dok.Journal of Immunology. - : American Association of Immunologists - ISSN 0022-1767
    Roč. 186, č. 6 (2011), s. 3373-3382
    Poč.str.10 s.
    Jazyk dok.eng - angličtina
    Země vyd.US - Spojené státy americké
    Klíč. slovaepigenetic change
    Vědní obor RIVEB - Genetika a molekulární biologie
    CEZAV0Z50070508 - ENTU-I, BC-A (2005-2011)
    UT WOS000287923500013
    DOI10.4049/jimmunol.1003216
    AnotacePlasticity within Th cell populations may play a role in enabling site-specific immune responses to infections while limiting tissue destruction. Epigenetic processes are fundamental to such plasticity; however, to date, most investigations have focused on in vitrogenerated T cells. In this study, we have examined the molecular mechanisms underpinning murine Th17 plasticity in vivo by assessing H3K4 and H3K27 trimethylation marks at Tbx21, Rorc, Il17a, Ifng, and Il12rb2 loci in purified ex vivo-isolated and in vitro-generated Th17 cells. Although both populations had largely comparable epigenetic signatures, including bivalent marks at Tbx21, freshly isolated ex vivo Th17 cells displayed restricted expression from Il12rb2 due to the presence of repressive chromatin modifications. This receptor, however, could be upregulated on isolated ex vivo Th17 cells after in vitro activation or by in vivo immunization and was augmented by the presence of IFN-g. Such activated cells could then be deviated toward a Th1-like profile. We show that IL-12 stimulation removes H3K27 trimethylation modifications at Tbx21/T-bet leading to enhanced T-bet expression with in vitro Th17 cells. Our study reveals important potential phenotypic differences between ex vivo- and in vitro-generated Th17 cells and provides mechanistic insight into Th17 cell plasticity.
    PracovištěBiologické centrum (od r. 2006)
    KontaktDana Hypšová, eje@eje.cz, Tel.: 387 775 214
    Rok sběru2012
Počet záznamů: 1  

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