Cutting edge:: Gab2 mediates an inhibitory phosphatidylinositol 3′-kinase pathway in T cell antigen receptor signaling

被引:56
作者
Pratt, JC
Igras, VE
Maeda, H
Baksh, S
Gelfand, EW
Burakoff, SJ
Neel, BG
Gu, HH
机构
[1] Beth Israel Deaconess Med Ctr, Dept Med, Div Hematol Oncol, Canc Biol Program, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Dept Pediat Oncol, Boston, MA 02115 USA
[3] Natl Jewish Med & Res Ctr, Dept Pediat, Div Cell Biol, Denver, CO 80206 USA
关键词
D O I
10.4049/jimmunol.165.8.4158
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Phosphatidylinositol 3'-kinase (PI3K) is a key component of multiple signaling pathways, where it typically promotes survival, proliferation, and/or adhesion. Here, we show that in TCR signaling, the scaffolding adapter Gab2 delivers an inhibitory signal via PI3K. Overexpression of Gab2 in T cell lines inhibits TCR-evoked activation of the IL-2 promoter, blocking NF-AT- and NF-kappa B-directed transcription. Inhibition is abrogated by mutating the Gab2 p85-binding sites, by treatment with PI3K inhibitors or by cotransfection of phosphatase homolog of tensin, Our findings provide the first evidence of a negative function for a scaffolding adapter in T cells and identify Gab2/PI3K-containing complexes as novel regulators of TCR signaling.
引用
收藏
页码:4158 / 4163
页数:6
相关论文
共 20 条
[1]   The small GTP-binding protein rho potentiates AP-1 transcription in T cells [J].
Chang, JH ;
Pratt, JC ;
Sawasdikosol, S ;
Kapeller, R ;
Burakoff, SJ .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (09) :4986-4993
[2]   Phosphoinositide 3-kinase regulation of T cell receptor-mediated interleukin-2 gene expression in normal T cells [J].
Eder, AM ;
Dominguez, L ;
Franke, TF ;
Ashwell, JD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (43) :28025-28031
[3]  
Gadina M, 2000, J BIOL CHEM, V275, P26959
[4]   Cloning of p97/Gab2, the major SHP2-binding protein in hematopoietic cells, reveals a novel pathway for cytokine-induced gene activation [J].
Gu, HH ;
Pratt, JC ;
Burakoff, SJ ;
Neel, BG .
MOLECULAR CELL, 1998, 2 (06) :729-740
[5]   RAS-DEPENDENT INDUCTION OF CELLULAR-RESPONSES BY CONSTITUTIVELY ACTIVE PHOSPHATIDYLINOSITOL-3 KINASE [J].
HU, QJ ;
KLIPPEL, A ;
MUSLIN, AJ ;
FANTL, WJ ;
WILLIAMS, LT .
SCIENCE, 1995, 268 (5207) :100-102
[6]   Transcriptional regulation of the interleukin-2 gene in normal human peripheral blood T cells - Convergence of costimulatory signals and differences from transformed T cells [J].
Hughes, CCW ;
Pober, JS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (10) :5369-5377
[7]   TRANSCRIPTIONAL REGULATION OF THE IL-2 GENE [J].
JAIN, J ;
LOH, C ;
RAO, A .
CURRENT OPINION IN IMMUNOLOGY, 1995, 7 (03) :333-342
[8]   A lipid-anchored Grb2-binding protein that links FGF-receptor activation to the Ras/MAPK signaling pathway [J].
Kouhara, H ;
Hadari, YR ;
SpivakKroizman, T ;
Schilling, J ;
BarSagi, D ;
Lax, I ;
Schlessinger, J .
CELL, 1997, 89 (05) :693-702
[9]   The tumor suppressor, PTEN/MMAC1, dephosphorylates the lipid second messenger, phosphatidylinositol 3,4,5-trisphosphate [J].
Maehama, T ;
Dixon, JE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (22) :13375-13378
[10]   A conserved inositol phospholipid binding site within the pleckstrin homology domain of the Gab1 docking protein is required for epithelial morphogenesis [J].
Maroun, CR ;
Moscatello, DK ;
Naujokas, MA ;
Holgado-Madruga, M ;
Wong, AJ ;
Park, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (44) :31719-31726