GRAIL:: An E3 ubiquitin ligase that inhibits cytokine gene transcription is expressed in anergic CD4+ T cells

被引:252
作者
Anandasabapathy, N
Ford, GS
Bloom, D
Holness, C
Paragas, V
Seroogy, C
Skrenta, H
Hollenhorst, M
Fathman, CG [1 ]
Soares, L
机构
[1] Stanford Univ, Sch Med, Dept Med, Div Rheumatol & Immunol, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Pathol, Stanford, CA 94305 USA
关键词
D O I
10.1016/S1074-7613(03)00084-0
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T cell anergy may serve to limit autoreactive T cell responses. We examined early changes in gene expression after antigen-TCR signaling in the presence (activation) or absence (anergy) of B7 costimulation. Induced expression of GRAIL (gene related to anergy in lymphocytes) was observed in anergic CD4(+) T cells. GRAIL is a type I transmembrane protein that localizes to the endocytic pathway and bears homology to RING zinc-finger proteins. Ubiquitination studies in vitro support GRAIL function as an E3 ubiquitin ligase. Expression of GRAIL in retrovirally transduced T cell hybridomas dramatically limits activation-induced IL-2 and IL-4 production. Additional studies suggest that GRAIL E3 ubiquitin ligase activity and intact endocytic trafficking are critical for cytokine transcriptional regulation. Expression of GRAIL after an anergizing stimulus may result in ubiquitin-mediated regulation of proteins essential for mitogenic cytokine expression, thus positioning GRAIL as a key player in the induction of the anergic phenotype.
引用
收藏
页码:535 / 547
页数:13
相关论文
共 62 条
[11]   Activation of the mitogen-activated protein kinase pathway by a Gq/11-coupled muscarinic receptor is independent of receptor internalization [J].
Budd, DC ;
Rae, A ;
Tobin, AB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (18) :12355-12360
[12]   Structural requirements for ligand binding by a probable plant vacuolar sorting receptor [J].
Cao, XF ;
Rogers, SW ;
Butler, J ;
Beevers, L ;
Rogers, JC .
PLANT CELL, 2000, 12 (04) :493-506
[13]   Endocytosis and signaling cascades: a close encounter [J].
Cavalli, V ;
Corti, M ;
Gruenberg, J .
FEBS LETTERS, 2001, 498 (2-3) :190-196
[14]   ACTIVATION-INDUCED UBIQUITINATION OF THE T-CELL ANTIGEN RECEPTOR [J].
CENCIARELLI, C ;
HOU, D ;
HSU, KC ;
RELLAHAN, BL ;
WIEST, DL ;
SMITH, HT ;
FRIED, VA ;
WEISSMAN, AM .
SCIENCE, 1992, 257 (5071) :795-797
[15]  
CHIANG YJ, 2002, NATURE, V403, P216
[16]  
Chuang E, 1997, J IMMUNOL, V159, P144
[17]   IMMUNOGLOBULIN SIGNAL-TRANSDUCTION GUIDES THE SPECIFICITY OF B-CELL T-CELL-INTERACTIONS AND IS BLOCKED IN TOLERANT SELF-REACTIVE B-CELLS [J].
COOKE, MP ;
HEATH, AW ;
SHOKAT, KM ;
ZENG, YJ ;
FINKELMAN, FD ;
LINSLEY, PS ;
HOWARD, M ;
GOODNOW, CC .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 179 (02) :425-438
[18]   The Rho-family GTP exchange factor Vav is a critical transducer of T cell receptor signals to the calcium, ERK, and NF-κB pathways [J].
Costello, PS ;
Walters, AE ;
Mee, PJ ;
Turner, M ;
Reynolds, LF ;
Prisco, A ;
Sarner, N ;
Zamoyska, R ;
Tybulewicz, VLJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (06) :3035-3040
[19]   Role of arrestins in endocytosis and signaling of α2-adrenergic receptor subtypes [J].
DeGraff, JL ;
Gagnon, AW ;
Benovic, JL ;
Orsini, MJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (16) :11253-11259
[20]   Anergic T cells are defective in both jun NH2-terminal kinase and mitogen-activated protein kinase signaling pathways [J].
DeSilva, DR ;
Feeser, WS ;
Tancula, EJ ;
Scherle, PA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (05) :2017-2023