The GTPase Rac-1 controls cell fate in the thymus by diverting thymocytes from positive to negative selection

被引:45
作者
Gomez, M
Kioussis, D
Cantrell, DA
机构
[1] Imperial Canc Res Fund, Lymphocyte Activat Lab, London WC2A 3PX, England
[2] Natl Inst Med Res, London NW7 1AA, England
关键词
D O I
10.1016/S1074-7613(01)00235-7
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 positive selection of CD4 or CD8 single-positive mature peripheral T lymphocytes and the deletion of self-reactive cells are crucial for central tolerance in the peripheral immune system. Previously, the guanine nucleotide binding protein Rac-1 has been shown to control pre-T cell development. The present report now describes the actions of Rac-1 in thymocyte selection. The study reveals that this molecule has the striking and unique ability to efficiently divert cells from positive selection into a pathway of negative selection and deletion. The ability of Rac-1 to switch thymocytes from a destiny of positive to negative selection identifies this molecule as a critical regulator of the developmental processes in T cells that are essential for immune homeostasis.
引用
收藏
页码:703 / 713
页数:11
相关论文
共 73 条
[41]   A BRAIN SERINE THREONINE PROTEIN-KINASE ACTIVATED BY CDC42 AND RAC1 [J].
MANSER, E ;
LEUNG, T ;
SALIHUDDIN, H ;
ZHAO, ZS ;
LIM, L .
NATURE, 1994, 367 (6458) :40-46
[42]   Bcl-2 can rescue T lymphocyte development in interleukin-7 receptor-deficient mice but not in mutant rag-1(-/-) mice [J].
Maraskovsky, E ;
OReilly, LA ;
Teepe, M ;
Corcoran, LM ;
Peschon, JJ ;
Strasser, A .
CELL, 1997, 89 (07) :1011-1019
[43]   Maturation versus death of developing double-positive thymocytes reflects competing effects on Bcl-2 expression and can be regulated by the intensity of CD28 costimulation [J].
McKean, DJ ;
Huntoon, CJ ;
Bell, MP ;
Tai, XG ;
Sharrow, S ;
Hedin, KE ;
Conley, A ;
Singer, A .
JOURNAL OF IMMUNOLOGY, 2001, 166 (05) :3468-3475
[44]   CD28 utilizes Vav-1 to enhance TCR-proximal signaling and NF-AT activation [J].
Michel, F ;
Mangino, G ;
Attal-Bonnefoy, G ;
Tuosto, L ;
Alcover, A ;
Roumier, A ;
Olive, D ;
Acuto, O .
JOURNAL OF IMMUNOLOGY, 2000, 165 (07) :3820-3829
[45]   SELECTIVE ACTIVATION OF THE JNK SIGNALING CASCADE AND C-JUN TRANSCRIPTIONAL ACTIVITY BY THE SMALL GTPASES RAC AND CDC42HS [J].
MINDEN, A ;
LIN, AN ;
CLARET, FX ;
ABO, A ;
KARIN, M .
CELL, 1995, 81 (07) :1147-1157
[46]   ESSENTIAL ROLE FOR ZAP-70 IN BOTH POSITIVE AND NEGATIVE SELECTION OF THYMOCYTES [J].
NEGISHI, I ;
MOTOYAMA, N ;
NAKAYAMA, K ;
NAKAYAMA, K ;
SENJU, S ;
HATAKEYAMA, S ;
ZHANG, Q ;
CHAN, AC ;
LOH, DY .
NATURE, 1995, 376 (6539) :435-438
[47]   RHO, RAC, AND CDC42 GTPASES REGULATE THE ASSEMBLY OF MULTIMOLECULAR FOCAL COMPLEXES ASSOCIATED WITH ACTIN STRESS FIBERS, LAMELLIPODIA, AND FILOPODIA [J].
NOBES, CD ;
HALL, A .
CELL, 1995, 81 (01) :53-62
[48]   THE ROLE OF P21(RAS) IN CD28 SIGNAL-TRANSDUCTION - TRIGGERING OF CD28 WITH ANTIBODIES, BUT NOT THE LIGAND B7-1, ACTIVATES P21(RAS) [J].
NUNES, JA ;
COLLETTE, Y ;
TRUNEH, A ;
OLIVE, D ;
CANTRELL, DA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (03) :1067-1076
[49]   DISTINCT SEQUENCE OF NEGATIVE OR POSITIVE SELECTION IMPLIED BY THYMOCYTE T-CELL RECEPTOR DENSITIES [J].
OHASHI, PS ;
PIRCHER, H ;
BURKI, K ;
ZINKERNAGEL, RM ;
HENGARTNER, H .
NATURE, 1990, 346 (6287) :861-863
[50]  
Page DM, 1999, J IMMUNOL, V163, P3577