CHARACTERIZATION OF THYMUS-DERIVED LYMPHOCYTES EXPRESSING TI-ALPHA-BETA-CD3-GAMMA-DELTA-EPSILON-ZETA-ZETA, TI-ALPHA-BETA-CD3-GAMMA-DELTA-EPSILON-ETA-ETA OR TI-ALPHA-BETA-CD3-GAMMA-DELTA-EPSILON-ZETA-ZETA-ZETA-ETA ANTIGEN RECEPTOR ISOFORMS - ANALYSIS BY GENE TRANSFECTION

被引:36
作者
CLAYTON, LK
BAUER, A
JIN, YJ
DADAMIO, L
KOYASU, S
REINHERZ, EL
机构
[1] HARVARD UNIV,SCH MED,DEPT PATHOL,BOSTON,MA 02115
[2] HARVARD UNIV,SCH MED,DEPT MED,BOSTON,MA 02115
关键词
D O I
10.1084/jem.172.4.1243
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To characterize the function of the CD3η subunit of the T cell receptor (TCR), we have used cDNAs encoding CD3ζ, CD3η, or both to reconstitute a variant of a cytochrome c-specific, I-Ek-restricted murine T cell hybridoma, termed MA5.8, which lacks CD3ζ and CD3η proteins. We provide direct evidence that assembly and surface expression of TCRs can be mediated by either of these subunits separately or together. However, the level of TCR expression on ζ transfectants is up to one order of magnitude greater than that on η transfectants, implying that CD3η is weakly associated with the pentameric Tiα-βCD3γδe complex and/or inefficient at salvaging the incomplete TCR from lysosomal degradation. As a component of the TCR, the CD3η subunit preferentially forms a heterodimer with CD3ζ, but is also able to form a CD3η-η homodimer. Crosslinking of Tiα-βCD3γδeζ-ζ, Tiα-βCD3γδeη-η, or Tiα-βCD3γδeζ-ζ/ζ-η-TCR isotypes with anti-CD3e monoclonal antibody or a cytochrome c peptide epitope on I-Ek antigen-presenting cells mediates signal transduction resulting in reversible cell-cycle arrest of transfected clones. Given the potential for diversity of signals generated by these functional TCR isotypes and the expression of the CD3 η gene product in the thymus, CD3η is likely to play a role in selection and/or activation of thymocytes during development. © 1990, Rockefeller University Press., All rights reserved.
引用
收藏
页码:1243 / 1253
页数:11
相关论文
共 33 条
  • [1] GENETIC AND MUTATIONAL ANALYSIS OF THE T-CELL ANTIGEN RECEPTOR
    ASHWELL, JD
    KLAUSNER, RD
    [J]. ANNUAL REVIEW OF IMMUNOLOGY, 1990, 8 : 139 - 167
  • [2] CELL-GROWTH CYCLE BLOCK OF T-CELL HYBRIDOMAS UPON ACTIVATION WITH ANTIGEN
    ASHWELL, JD
    CUNNINGHAM, RE
    NOGUCHI, PD
    HERNANDEZ, D
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1987, 165 (01) : 173 - 194
  • [3] BANIYASH M, 1989, J BIOL CHEM, V264, P13252
  • [4] BANIYASH M, 1988, J BIOL CHEM, V263, P9874
  • [5] SELECTIVE DEGRADATION OF T-CELL ANTIGEN RECEPTOR CHAINS RETAINED IN A PRE-GOLGI COMPARTMENT
    CHEN, C
    BONIFACINO, JS
    YUAN, LC
    KLAUSNER, RD
    [J]. JOURNAL OF CELL BIOLOGY, 1988, 107 (06) : 2149 - 2161
  • [6] THE T-CELL RECEPTOR/CD3 COMPLEX - A DYNAMIC PROTEIN ENSEMBLE
    CLEVERS, H
    ALARCON, B
    WILEMAN, T
    TERHORST, C
    [J]. ANNUAL REVIEW OF IMMUNOLOGY, 1988, 6 : 629 - 662
  • [7] T-CELL ANTIGEN RECEPTOR GENES AND T-CELL RECOGNITION
    DAVIS, MM
    BJORKMAN, PJ
    [J]. NATURE, 1988, 334 (6181) : 395 - 402
  • [8] MATHEMATICAL-ANALYSIS OF DNA DISTRIBUTIONS DERIVED FROM FLOW MICROFLUOROMETRY
    DEAN, PN
    JETT, JH
    [J]. JOURNAL OF CELL BIOLOGY, 1974, 60 (02) : 523 - 527
  • [9] A TECHNIQUE FOR RADIOLABELING DNA RESTRICTION ENDONUCLEASE FRAGMENTS TO HIGH SPECIFIC ACTIVITY
    FEINBERG, AP
    VOGELSTEIN, B
    [J]. ANALYTICAL BIOCHEMISTRY, 1983, 132 (01) : 6 - 13
  • [10] THE GENE ENCODING THE EPSILON-SUBUNIT OF THE T3 T-CELL RECEPTOR COMPLEX MAPS TO CHROMOSOME-11 IN HUMANS AND TO CHROMOSOME-9 IN MICE
    GOLD, DP
    VANDONGEN, JJM
    MORTON, CC
    BRUNS, GAP
    VANDENELSEN, P
    VANKESSEL, AHMG
    TERHORST, C
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (06) : 1664 - 1668