SURFACE EXPRESSION OF ONLY GAMMA-DELTA AND OR ALPHA-BETA-T-CELL RECEPTOR HETERODIMERS BY CELLS WITH 4 (ALPHA, BETA, GAMMA, DELTA) FUNCTIONAL RECEPTOR CHAINS

被引:50
作者
SAITO, T
HOCHSTENBACH, F
MARUSICGALESIC, S
KRUISBEEK, AM
BRENNER, M
GERMAIN, RN
机构
[1] NCI, BIOL RESPONSE MODIFIERS PROGRAM, BETHESDA, MD 20892 USA
[2] HARVARD UNIV, SCH MED, DANA FARBER CANC INST, DIV TUMOR VIROL, BOSTON, MA 02115 USA
[3] HARVARD UNIV, BRIGHAM & WOMENS HOSP, SCH MED, DEPT RHEUMATOL & IMMUNOL, BOSTON, MA 02115 USA
关键词
D O I
10.1084/jem.168.3.1003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Surface expression of TCR dimers by cells synthesizing three or four distinct types of receptor chains was analyzed. Cells containing intact .gamma., .alpha., and .beta. chains had only .gamma..delta. dimers on the cell surface. In human PEER cells, addition of a functional .alpha. chain led to the loss of .gamma..delta. dimer expression and expression of only .alpha..beta. dimers. This result was not due to transcriptional down-regulation of the .gamma. or .delta. loci. In murine cells expressing all four chains, both .gamma..delta. and .alpha..beta. dimers could be demonstrated on a single cell. No other chain combinations (.alpha..gamma., .alpha..delta., .beta..gamma., or .beta..delta.) were detected. Thus, there is stringent control of assembly and/or transport of TCR heterodimers, such that functional receptors consist only of .alpha..beta. and .gamma..delta. pairs, and no additional repertoire diversity is generated by cross pairing.
引用
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页码:1003 / 1020
页数:18
相关论文
共 53 条
[1]   DIVERSITY AND STRUCTURE OF GENES OF THE ALPHA-FAMILY OF MOUSE T-CELL ANTIGEN RECEPTOR [J].
ARDEN, B ;
KLOTZ, JL ;
SIU, G ;
HOOD, LE .
NATURE, 1985, 316 (6031) :783-787
[2]   IMMUNOCHEMICAL PROOF THAT A NOVEL REARRANGING GENE ENCODES THE T-CELL RECEPTOR-DELTA SUBUNIT [J].
BAND, H ;
HOCHSTENBACH, F ;
MCLEAN, J ;
HATA, S ;
KRANGEL, MS ;
BRENNER, MB .
SCIENCE, 1987, 238 (4827) :682-684
[3]   A FUNCTIONAL T3 MOLECULE ASSOCIATED WITH A NOVEL HETERODIMER ON THE SURFACE OF IMMATURE HUMAN THYMOCYTES [J].
BANK, I ;
DEPINHO, RA ;
BRENNER, MB ;
CASSIMERIS, J ;
ALT, FW ;
CHESS, L .
NATURE, 1986, 322 (6075) :179-181
[4]   THE MURINE T-CELL RECEPTOR USES A LIMITED REPERTOIRE OF EXPRESSED V-BETA GENE SEGMENTS [J].
BARTH, RK ;
KIM, BS ;
LAN, NC ;
HUNKAPILLER, T ;
SOBIECK, N ;
WINOTO, A ;
GERSHENFELD, H ;
OKADA, C ;
HANSBURG, D ;
WEISSMAN, IL ;
HOOD, L .
NATURE, 1985, 316 (6028) :517-523
[5]   CHARACTERIZATION OF MURINE THYMOCYTES WITH CD3-ASSOCIATED T-CELL RECEPTOR STRUCTURES [J].
BLUESTONE, JA ;
PARDOLL, D ;
SHARROW, SO ;
FOWLKES, BJ .
NATURE, 1987, 326 (6108) :82-84
[6]   FILM DETECTION METHOD FOR TRITIUM-LABELED PROTEINS AND NUCLEIC-ACIDS IN POLYACRYLAMIDE GELS [J].
BONNER, WM ;
LASKEY, RA .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1974, 46 (01) :83-88
[7]   SYNCHRONIZED REARRANGEMENT OF T-CELL GAMMA-CHAIN AND BETA-CHAIN GENES IN FETAL THYMOCYTE DEVELOPMENT [J].
BORN, W ;
RATHBUN, G ;
TUCKER, P ;
MARRACK, P ;
KAPPLER, J .
SCIENCE, 1986, 234 (4775) :479-482
[9]  
BRENNER MB, 1987, J IMMUNOL, V138, P1502
[10]   2 FORMS OF THE T-CELL RECEPTOR GAMMA-PROTEIN FOUND ON PERIPHERAL-BLOOD CYTOTOXIC T-LYMPHOCYTES [J].
BRENNER, MB ;
MCLEAN, J ;
SCHEFT, H ;
RIBERDY, J ;
ANG, SL ;
SEIDMAN, JG ;
DEVLIN, P ;
KRANGEL, MS .
NATURE, 1987, 325 (6106) :689-694