IL-4-activated STAT-6 inhibits IFN-γ-induced CD40 gene expression in macrophages/microglia

被引:65
作者
Nguyen, VT [1 ]
Benveniste, EN [1 ]
机构
[1] Univ Alabama Birmingham, Dept Cell Biol, Birmingham, AL 35294 USA
关键词
D O I
10.4049/jimmunol.165.11.6235
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The antagonism between the cytokines IFN-gamma and IL-4 is well documented, but the mechanism by which IL-4 inhibits IFN-gamma -induced gene expression is not clearly understood. CD40 is a type I transmembrane protein that is critical for proper functioning of the immune system. We have previously shown that IFN-gamma is the most potent inducer of CD40 expression by macrophages and microglia, In this report, we describe the molecular mechanisms by which IL-4 inhibits IFN-gamma -induced CD40 expression. IL-4 suppresses IFN-gamma -induced CD40 gene expression in both macrophages and microglia, and such inhibition is dependent on the activation of STAT-6. Nuclear run-on and transfection studies indicate that IL-4-mediated repression is at the transcriptional level. Furthermore, IL-4 inhibition of IFN-gamma induced CD40 expression is specific, since IL-4 does not inhibit IFN-gamma -induced IFN-responsive factor-1 gene expression. Site directed mutagenesis studies demonstrate that two STAT binding sites, named proximal and distal IFN-gamma -activated sequences, in the human CD40 promoter are important for IL-4 inhibition of IFN-gamma -induced CD40 promoter activity, Moreover, EMSAs indicate that IL-4-activated STAT-6 binds to these two STAT binding sites. These results suggest that IL-4 inhibition of IFN-gamma -induced CD40 gene expression is mediated by direct STAT-6 binding to the CD40 promoter.
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页码:6235 / 6243
页数:9
相关论文
共 65 条
[51]   ROLE OF IRS-2 IN INSULIN AND CYTOKINE SIGNALING [J].
SUN, XJ ;
WANG, LM ;
ZHANG, YT ;
YENUSH, L ;
MYERS, MG ;
GLASHEEN, E ;
LANE, WS ;
PIERCE, JH ;
WHITE, MF .
NATURE, 1995, 377 (6545) :173-177
[52]   Regulation of the interleukin (IL)-12R beta 2 subunit expression in developing T helper 1 (Th1) and Th2 cells [J].
Szabo, SJ ;
Dighe, AS ;
Gubler, U ;
Murphy, KM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (05) :817-824
[53]   Essential role of Stat6 in IL-4 signalling [J].
Takeda, K ;
Tanaka, T ;
Shi, W ;
Matsumoto, M ;
Minami, M ;
Kashiwamura, S ;
Nakanishi, K ;
Yoshida, N ;
Kishimoto, T ;
Akira, S .
NATURE, 1996, 380 (6575) :627-630
[54]  
TEVELDE AA, 1990, BLOOD, V76, P1392
[55]  
VELDE AAT, 1990, J IMMUNOL, V144, P3046
[56]   DNA binding of in vitro activated Stat1 alpha, Stat1 beta and truncated Stat1: Interaction between NH2-terminal domains stabilizes binding of two dimers to tandem DNA sites [J].
Vinkemeier, U ;
Cohen, SL ;
Moarefi, I ;
Chait, BT ;
Kuriyan, J ;
Darnell, JE .
EMBO JOURNAL, 1996, 15 (20) :5616-5626
[57]   CD40 and its crucial role as a member of the TNFR family [J].
Vogel, LA ;
Noelle, RJ .
SEMINARS IN IMMUNOLOGY, 1998, 10 (06) :435-442
[58]   Mouse microglial cell lines differing in constitutive and interferon-gamma-inducible antigen-presenting activities for naive and memory CD4(+) and CD8(+) T cells [J].
Walker, WS ;
Gatewood, J ;
Olivas, E ;
Askew, D ;
Havenith, CEG .
JOURNAL OF NEUROIMMUNOLOGY, 1995, 63 (02) :163-174
[59]   Neurotrophins and the anti-inflammatory agents interleukin-4 (IL-4), IL-10, IL-11 and transforming growth factor-β1 (TGF-β1) down-regulate T cell costimulatory molecules B7 and CD40 on cultured rat microglia [J].
Wei, RT ;
Jonakait, GM .
JOURNAL OF NEUROIMMUNOLOGY, 1999, 95 (1-2) :8-18
[60]   MAXIMAL ACTIVATION OF TRANSCRIPTION BY STAT1 AND STAT3 REQUIRES BOTH TYROSINE AND SERINE PHOSPHORYLATION [J].
WEN, ZL ;
ZHONG, Z ;
DARNELL, JE .
CELL, 1995, 82 (02) :241-250