NFIL3/E4BP4 controls type 2 T helper cell cytokine expression

被引:81
作者
Kashiwada, Masaki [1 ]
Cassel, Suzanne L. [1 ]
Colgan, John D. [1 ]
Rothman, Paul B. [1 ]
机构
[1] Univ Iowa, Dept Internal Med, Roy J & Lucille A Carver Coll Med, Iowa City, IA 52242 USA
基金
美国国家卫生研究院;
关键词
helper T-cell differentiation; IL-13; IL-4; transcriptional regulation; TRANSCRIPTION FACTOR; GENE-EXPRESSION; IL-4; EXPRESSION; TGF-BETA; IDENTIFICATION; DIFFERENTIATION; CHROMATIN; PROMOTES; E4BP4; INTERLEUKIN-13;
D O I
10.1038/emboj.2011.111
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Type 2 T helper (T(H)2) cells are critical for the development of allergic immune responses; however, the molecular mechanism controlling their effector function is still largely unclear. Here, we report that the transcription factor NFIL3/E4BP4 regulates cytokine production and effector function by T(H)2 cells. NFIL3 is highly expressed in T(H)2 cells but much less in T(H)1 cells. Production of interleukin (IL)-13 and IL-5 is significantly increased in Nfil3(-/-) T(H)2 cells and is decreased by expression of NFIL3 in wild-type T(H)2 cells. NFIL3 directly binds to and negatively regulates the Il13 gene. In contrast, IL-4 production is decreased in Nfil3(-/-) T(H)2 cells. Increased IL-13 and IL-5 together with decreased IL-4 production by antigen-stimulated splenocytes from the immunized Nfil3(-/-) mice was also observed. The ability of NFIL3 to alter T(H)2 cytokine production is a T-cell intrinsic effect. Taken together, these data indicate that NFIL3 is a key regulator of T(H)2 responses. The EMBO Journal (2011) 30, 2071-2082. doi: 10.1038/emboj.2011.111; Published online 15 April 2011
引用
收藏
页码:2071 / 2082
页数:12
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