THE T-CELL RECEPTOR AS A MULTICOMPONENT SIGNALING MACHINE - CD4/CD8 CORECEPTORS AND CD45 IN T-CELL ACTIVATION

被引:366
作者
JANEWAY, CA [1 ]
机构
[1] HOWARD HUGHES MED INST, NEW HAVEN, CT 06510 USA
关键词
TYROSINE KINASE; TYROSINE PHOSPHATASE; IMMUNOLOGICAL MEMORY; T-CELL DEVELOPMENT; NEGATIVE SIGNALING;
D O I
10.1146/annurev.immunol.10.1.645
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 T cell receptor is a multicomponent signalling machine. The three main components are the hypervariable alpha:beta-heterodimer that confers specificity and its attendant invariant chains CD3 gamma, delta, and epsilon and the zeta:zeta or zeta:eta, the CD4 or CD8 coreceptor, and CD45. Each of these components is required for efficient signal transduction, and each has relevant enzymatic activity associated with it. The invariant part of T cell receptor is associated with the tyrosine kinase p59fyn, the coreceptors are associated with the tyrosine kinase p56lck, and the cytoplasmic domain of CD45 has tyrosine-specific phosphatase activity. Moreover, there is strong evidence that these components interact in the plane of the membrane, and that these interactions are relevant for signal transduction. Finally, changes in the structure of CD45 that occur during differentiation of T cells alter the interactions of these three components of the signal transducing machinery, perhaps accounting for changes in signal transduction that accompany T-cell development in the thymus and the development of immunological memory cells.
引用
收藏
页码:645 / 674
页数:30
相关论文
共 147 条
  • [31] Fleury S G, 1991, Semin Immunol, V3, P177
  • [32] MOLECULAR AND CELLULAR EVENTS OF T-CELL DEVELOPMENT
    FOWLKES, BJ
    PARDOLL, DM
    [J]. ADVANCES IN IMMUNOLOGY, 1989, 44 : 207 - 264
  • [33] DELETION OF SELF-REACTIVE THYMOCYTES OCCURS AT A CD4+8+ PRECURSOR STAGE
    FOWLKES, BJ
    SCHWARTZ, RH
    PARDOLL, DM
    [J]. NATURE, 1988, 334 (6183) : 620 - 623
  • [34] CD8 IS NEEDED FOR DEVELOPMENT OF CYTOTOXIC T-CELLS BUT NOT HELPER T-CELLS
    FUNGLEUNG, WP
    SCHILHAM, MW
    RAHEMTULLA, A
    KUNDIG, TM
    VOLLENWEIDER, M
    POTTER, J
    VANEWIJK, W
    MAK, TW
    [J]. CELL, 1991, 65 (03) : 443 - 449
  • [35] RECONSTITUTION OF MHC CLASS-I SPECIFICITY BY TRANSFER OF THE T-CELL RECEPTOR AND LYT-2 GENES
    GABERT, J
    LANGLET, C
    ZAMOYSKA, R
    PARNES, JR
    SCHMITTVERHULST, AM
    MALISSEN, B
    [J]. CELL, 1987, 50 (04) : 545 - 554
  • [36] FUNCTIONAL INTERACTION BETWEEN HUMAN T-CELL PROTEIN CD4 AND THE MAJOR HISTOCOMPATIBILITY COMPLEX HLA-DR ANTIGEN
    GAY, D
    MADDON, P
    SEKALY, R
    TALLE, MA
    GODFREY, M
    LONG, E
    GOLDSTEIN, G
    CHESS, L
    AXEL, R
    KAPPLER, J
    MARRACK, P
    [J]. NATURE, 1987, 328 (6131) : 626 - 629
  • [37] GAY D, 1986, J IMMUNOL, V136, P2026
  • [38] THE T-CELL ACCESSORY MOLECULE CD4 RECOGNIZES A MONOMORPHIC DETERMINANT ON ISOLATED IA
    GAY, D
    BUUS, S
    PASTERNAK, J
    KAPPLER, J
    MARRACK, P
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (15) : 5629 - 5633
  • [39] GILLITZER R, 1990, J IMMUNOL, V144, P66
  • [40] REQUIREMENT FOR ASSOCIATION OF P56LCK WITH CD4 IN ANTIGEN-SPECIFIC SIGNAL TRANSDUCTION IN T-CELLS
    GLAICHENHAUS, N
    SHASTRI, N
    LITTMAN, DR
    TURNER, JM
    [J]. CELL, 1991, 64 (03) : 511 - 520