GATA-3 suppresses Th1 development by downregulation of Stat4 and not through effects on IL-12Rβ2 chain or T-bet

被引:214
作者
Usui, T [1 ]
Nishikomori, R [1 ]
Kitani, A [1 ]
Strober, W [1 ]
机构
[1] NIAID, Mucosal Immun Sect, Clin Invest Lab, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1016/S1074-7613(03)00057-8
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To further understand the interaction among GATA-3, Stat4, and T-bet in helper T cell development, we first showed that retroviral expression of GATA-3 in developing Th1 cells suppresses Th1 development through downregulation of Stat4 rather through downregulation of the IL-12Rbeta2 chain. Correspondingly, Stat4 levels are greatly suppressed during physiological Th2 development. Then, using cells doubly infected with GFP- and YFP-expressing retroviruses, we showed that retroviral GATA-3 expression in developing Th1 cells does not block Th1 development in cells coexpressing Stat4 but does so in cells coexpressing T-bet. Finally, we showed that retroviral Stat4 expression could facilitate Th2-->Th1 conversion in cells bearing an IL-12Rbeta2 transgene, even in cells lacking T-bet. These findings reassert that Stat4 signaling is a central element of Th1/Th2 development.
引用
收藏
页码:415 / 428
页数:14
相关论文
共 35 条
[1]   T-bet is a STAT1-induced regulator of IL-12R expression in naive CD4+ T cells [J].
Afkarian, M ;
Sedy, JR ;
Yang, J ;
Jacobson, NG ;
Cereb, N ;
Yang, SY ;
Murphy, TL ;
Murphy, KM .
NATURE IMMUNOLOGY, 2002, 3 (06) :549-557
[2]   Gene microarrays reveal extensive differential gene expression in both CD4+ and CD8+ type 1 and type 2 T cells [J].
Chtanova, T ;
Kemp, RA ;
Sutherland, APR ;
Ronchese, F ;
Mackay, CR .
JOURNAL OF IMMUNOLOGY, 2001, 167 (06) :3057-3063
[3]   GATA-3 significantly downregulates IFN-γ production from developing Th1 cells in addition to inducing IL4-and IL-5 levels [J].
Ferber, IA ;
Lee, HJ ;
Zonin, F ;
Heath, V ;
Mui, A ;
Arai, N ;
O'Garra, A .
CLINICAL IMMUNOLOGY, 1999, 91 (02) :134-144
[4]  
Glimcher LH, 2000, GENE DEV, V14, P1693
[5]   Early transcription and silencing of cytokine genes underlie polarization of T helper cell subsets [J].
Grogan, JL ;
Mohrs, M ;
Harmon, B ;
Lacy, DA ;
Sedat, JW ;
Locksley, RM .
IMMUNITY, 2001, 14 (03) :205-215
[6]   Cutting edge:: Ectopic expression of the IL-12 receptor-β2 in developing and committed Th2 cells does not affect the production of IL-4 or induce the production of IFN-γ [J].
Heath, VL ;
Showe, L ;
Crain, C ;
Barrat, FJ ;
Trinchieri, G ;
O'Garra, A .
JOURNAL OF IMMUNOLOGY, 2000, 164 (06) :2861-2865
[7]   DEVELOPMENT OF TH1 CD4+ T-CELLS THROUGH IL-12 PRODUCED BY LISTERIA-INDUCED MACROPHAGES [J].
HSIEH, CS ;
MACATONIA, SE ;
TRIPP, CS ;
WOLF, SF ;
OGARRA, A ;
MURPHY, KM .
SCIENCE, 1993, 260 (5107) :547-549
[8]   DIFFERENTIAL REGULATION OF T-HELPER PHENOTYPE DEVELOPMENT BY INTERLEUKIN-4 AND INTERLEUKIN-10 IN AN ALPHA-BETA-T-CELL-RECEPTOR TRANSGENIC SYSTEM [J].
HSIEH, CS ;
HEIMBERGER, AB ;
GOLD, JS ;
OGARRA, A ;
MURPHY, KM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (13) :6065-6069
[9]   INTERLEUKIN-12 SIGNALING IN T-HELPER TYPE-1 (TH1) CELLS INVOLVES TYROSINE PHOSPHORYLATION OF SIGNAL TRANSDUCER AND ACTIVATOR OF TRANSCRIPTION (STAT)3 AND STAT4 [J].
JACOBSON, NG ;
SZABO, SJ ;
WEBERNORDT, RM ;
ZHONG, Z ;
SCHREIBER, RD ;
DARNELL, JE ;
MURPHY, KM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 181 (05) :1755-1762
[10]   Stat6 is required for mediating responses to IL-4 and for the development of Th2 cells [J].
Kaplan, MH ;
Schindler, U ;
Smiley, ST ;
Grusby, MJ .
IMMUNITY, 1996, 4 (03) :313-319