CCAAT/Enhancer-Binding Protein α Negatively Regulates IFN-γ Expression in T Cells
Author(s) -
Shinya Tanaka,
Kentaro Tanaka,
Fay Magnusson,
Yeonseok Chung,
Gustavo Martínez,
Yi-Hong Wang,
Roza Nurieva,
Tomohiro Kurosaki,
Chen Dong
Publication year - 2014
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1303422
Subject(s) - germinal center , transcription factor , biology , ccaat enhancer binding proteins , cebpa , microbiology and biotechnology , t cell , somatic hypermutation , transcription (linguistics) , leucine zipper , enhancer , b cell , gene , immune system , dna binding protein , antibody , immunology , genetics , linguistics , philosophy
Humoral immunity, including Ab switching and somatic hypermutation, is critically regulated by CD4(+) T cells. T follicular helper (Tfh) cells have been recently shown to be a distinct T cell subset important in germinal center reactions. The transcriptional regulation of Tfh cell development and function has not been well understood. In this study, we report that C/EBPα, a basic region/leucine zipper transcription factor, is highly expressed in Tfh cells. Cebpa-deficient CD4(+) T cells exhibit enhanced IFN-γ expression in vitro and in vivo. T cell-specific Cebpa knockout mice, although not defective in Tfh cell generation, produce significantly increased levels of IgG2a/b and IgG3 following immunization with a protein Ag. Moreover, C/EBPα binds to the Ifng gene and inhibits T-bet-driven Ifng transcription in a DNA binding-dependent manner. Our study thus demonstrates that C/EBPα restricts IFN-γ expression in T cells to allow proper class switching by B cells.
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