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Blimp-1 attenuates Th1 differentiation by direct repression of ifng, tbx21 and bcl6 gene expression.

  • Erna Magnúsdóttir
  • , Luisa Cimmino
  • , G. A. Martins
  • , J. Liao
  • , G. Grunig
  • , K. R. Perez
  • , K. Calame
  • , Rocio K. Perez

Rannsóknarafurð: Framlag til fræðitímaritsGreinritrýni

Útdráttur

T cell-specific deletion of Blimp-1 causes abnormal T cell homeostasis and function, leading to spontaneous, fatal colitis in mice. Herein we explore the role of Blimp-1 in Th1/Th2 differentiation. Blimp-1 mRNA and protein are more highly expressed in Th2 cells compared with Th1 cells, and Blimp-1 attenuates IFN-γ production in CD4 cells activated under nonpolarizing conditions. Although Blimp-1-deficient T cells differentiate normally to Th2 cytokines in vitro, Blimp-1 is required in vivo for normal Th2 humoral responses to NP-KLH (4-hydroxy-3-nitrophenylacetyl/keyhole lymphocyte hemocyanin) immunization. Lack of Blimp-1 in CD4 T cells causes increased IFN-γ, T-bet, and Bcl-6 mRNA. By chromatin immunoprecipitation we show that Blimp-1 binds directly to a distal regulatory region in the ifng gene and at multiple sites in tbx21 and bcl6 genes. Our data provide evidence that Blimp-1 functions in Th2 cells to reinforce Th2 differentiation by repressing critical Th1 genes.

Upprunalegt tungumálEnska
Síður (frá-til)2338-2347
Síðufjöldi10
FræðitímaritJournal of Immunology
Bindi181
Númer tölublaðs4
DOI
ÚtgáfustaðaÚtgefið - 15 ágú. 2008

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