T-cell receptor signal transmission: who gives an ITAM?

被引:142
作者
Pitcher, LA
van Oers, NSC
机构
[1] Univ Texas, SW Med Ctr, Ctr Immunol, Dallas, TX 75390 USA
[2] Univ Texas, SW Med Ctr, Dept Microbiol, Dallas, TX 75390 USA
关键词
D O I
10.1016/j.it.2003.08.003
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 cells have an amazing ability to discern and differentially respond to MHC-embedded peptides that can differ by only a single amino acid. This potential involves a combination of the precise ligand-binding specificities of the T-cell receptor (TCR) and the distinct intracellular signaling processes it transmits. Signaling processes are controlled by the ten immunoreceptor tyrosine-based activation motifs (ITAMs) present in the invariant chains of the TCR complex (TCR zeta and CD3-gamma, -delta and -epsilon). Here, we discuss recent studies of the functions of TCR invariant chains and the contribution of the ten ITAMs to T-cell signal transmission. We incorporate these results into two non-exclusive models of TCR signal transduction: the ITAM multiplicity model, which describes a functional redundancy within the TCR zeta and CD3 ITAMs; and the differential signaling model, which proposes distinct functions for the CD3-gamma, -delta and -epsilon and TCR zeta modules.
引用
收藏
页码:554 / 560
页数:7
相关论文
共 58 条
[31]   Critical relationship between TCR signaling potential and TCR affinity during thymocyte selection [J].
Love, PE ;
Lee, J ;
Shores, EW .
JOURNAL OF IMMUNOLOGY, 2000, 165 (06) :3080-3087
[32]   ZETA-PHOSPHORYLATION WITHOUT ZAP-70 ACTIVATION-INDUCED BY TCR ANTAGONISTS OR PARTIAL AGONISTS [J].
MADRENAS, J ;
WANGE, RL ;
WANG, JL ;
ISAKOV, N ;
SAMELSON, LE ;
GERMAIN, RN .
SCIENCE, 1995, 267 (5197) :515-518
[33]   AN INTEGRAL MEMBRANE-PROTEIN (LMP2) BLOCKS REACTIVATION OF EPSTEIN-BARR-VIRUS FROM LATENCY FOLLOWING SURFACE-IMMUNOGLOBULIN CROSS-LINKING [J].
MILLER, CL ;
LEE, JH ;
KIEFF, E ;
LONGNECKER, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (02) :772-776
[34]   The protein interactions of the immunoglobulin receptor family tyrosine-based activation motifs present in the T cell receptor zeta subunits and the CD3 gamma, delta and epsilon chains [J].
Osman, N ;
Turner, H ;
Lucas, S ;
Reif, K ;
Cantrell, DA .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1996, 26 (05) :1063-1068
[35]   A novel Src homology 2 domain-containing molecule, Src-like adapter protein-2 (SLAP-2), which negatively regulates T cell receptor signaling [J].
Pandey, A ;
Ibarrola, N ;
Kratchmarova, I ;
Fernandez, MM ;
Constantinescu, SN ;
Ohara, O ;
Sawasdikosol, S ;
Lodish, HF ;
Mann, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (21) :19131-19138
[36]   T cell antagonism is functionally uncoupled from the 21- and 23-kDa tyrosine-phosphorylated TCR ζ subunits [J].
Pitcher, LA ;
Ohashi, PS ;
van Oers, NSC .
JOURNAL OF IMMUNOLOGY, 2003, 171 (02) :845-852
[37]   The formation and functions of the 21- and 23-kDa tyrosine-phosphorylated TCRζ subunits [J].
Pitcher, LA ;
Young, JA ;
Mathis, MA ;
Wrage, PC ;
Bartók, B ;
van Oers, NSC .
IMMUNOLOGICAL REVIEWS, 2003, 191 (01) :47-61
[38]   INTERACTION OF SHC WITH THE ZETA-CHAIN OF THE T-CELL RECEPTOR UPON T-CELL ACTIVATION [J].
RAVICHANDRAN, KS ;
LEE, KK ;
ZHOU, SY ;
CANTLEY, LC ;
BURN, P ;
BURAKOFF, SJ .
SCIENCE, 1993, 262 (5135) :902-905
[39]   SEQUENCE REQUIREMENTS FOR INDUCTION OF CYTOLYSIS BY THE T-CELL ANTIGEN/FC RECEPTOR ZETA-CHAIN [J].
ROMEO, C ;
AMIOT, M ;
SEED, B .
CELL, 1992, 68 (05) :889-897
[40]   CELLULAR-IMMUNITY TO HIV ACTIVATED BY CD4 FUSED TO T-CELL OR FC RECEPTOR POLYPEPTIDES [J].
ROMEO, C ;
SEED, B .
CELL, 1991, 64 (05) :1037-1046