PREFERENTIAL POSITIVE SELECTION OF V-ALPHA-2+CD8+ T-CELLS IN MOUSE STRAINS EXPRESSING BOTH H-2K AND T-CELL RECEPTOR V-ALPHA-A HAPLOTYPES - DETERMINATION WITH A V-ALPHA-2-SPECIFIC MONOCLONAL-ANTIBODY

被引:94
作者
PIRCHER, H
REBAI, N
GROETTRUP, M
GREGOIRE, C
SPEISER, DE
HAPP, MP
PALMER, E
ZINKERNAGEL, RM
HENGARTNER, H
MALISSEN, B
机构
[1] CNRS,INSERM,CTR IMMUNOL,MARSEILLE,FRANCE
[2] NATL JEWISH CTR IMMUNOL & RESP MED,DEPT PEDIAT,DENVER,CO
关键词
D O I
10.1002/eji.1830220217
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A monoclonal antibody, B20.1, was generated by fusing spleen cells from a Lou rat immunized with a soluble alpha/beta-T cell receptor (TcR; V(alpha)2/V(beta)2) to mouse myeloma cells. Analysis of a panel of V(alpha)2 mRNA-expressing T cell lines, hybridomas and transfectants revealed that the B20.1 antibody was specific for murine TcR V(alpha)2 chains. The V(alpha)2+ T cell population was examined in various inbred strains by two-color immunofluorescence using B20.1 and CD4- and CD8-specific antibodies with the following results: (a) the B20.1 antibody detected most members of the TcR V(alpha)2 subfamily in the four TcR V(alpha) haplotypes tested; (b) in most strains examined, TcR V(alpha)2 expression was biased to the CD4 subset (7.4%-17.4% V(alpha)2+ T cells) as compared to the CD8 compartment (3.8%-13.3%); (c) TcR V(alpha)2 expression was not influenced by Mls gene products and (d) increased positive selection of V(alpha)2+ CD8+ T cells by H-2k major histocompatibility complex molecules occurred in all murine strains tested of the TcR V(alpha)a, but not in those bearing the TcR V(alpha)b haplotype.
引用
收藏
页码:399 / 404
页数:6
相关论文
共 32 条
[1]   INTERACTIONS BETWEEN MHC-ENCODED PRODUCTS AND CLONED T-CELLS .1. FINE SPECIFICITY OF INDUCTION OF PROLIFERATION AND LYSIS [J].
ALBERT, F ;
BUFERNE, M ;
BOYER, C ;
SCHMITTVERHULST, AM .
IMMUNOGENETICS, 1982, 16 (06) :533-549
[2]   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
[3]   AN ANALYSIS OF T-CELL RECEPTOR VARIABLE REGION GENE-EXPRESSION IN MAJOR HISTOCOMPATIBILITY COMPLEX DISPARATE MICE [J].
BILL, J ;
APPEL, VB ;
PALMER, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (23) :9184-9188
[4]   THE T-CELL REPERTOIRE MAY BE BIASED IN FAVOR OF MHC RECOGNITION [J].
BLACKMAN, M ;
YAGUE, J ;
KUBO, R ;
GAY, D ;
COLECLOUGH, C ;
PALMER, E ;
KAPPLER, J ;
MARRACK, P .
CELL, 1986, 47 (03) :349-357
[5]   INFLUENCE OF THE MAJOR HISTOCOMPATIBILITY COMPLEX ON POSITIVE THYMIC SELECTION OF V-BETA-17A+ T-CELLS [J].
BLACKMAN, MA ;
MARRACK, P ;
KAPPLER, J .
SCIENCE, 1989, 244 (4901) :214-217
[6]   T-CELL ANTIGEN RECEPTOR GENES AND T-CELL RECOGNITION [J].
DAVIS, MM ;
BJORKMAN, PJ .
NATURE, 1988, 334 (6181) :395-402
[7]  
ELLIOTT JF, 1988, NATURE, V331, P627
[8]   RECONSTITUTION OF MHC CLASS-I SPECIFICITY BY TRANSFER OF THE T-CELL RECEPTOR AND LYT-2 GENES [J].
GABERT, J ;
LANGLET, C ;
ZAMOYSKA, R ;
PARNES, JR ;
SCHMITTVERHULST, AM ;
MALISSEN, B .
CELL, 1987, 50 (04) :545-554
[9]   LIMITED RECEPTOR REPERTOIRE IN A MYCOBACTERIA-REACTIVE SUBSET OF GAMMA-DELTA-LYMPHOCYTES [J].
HAPP, MP ;
KUBO, RT ;
PALMER, E ;
BORN, WK ;
OBRIEN, RL .
NATURE, 1989, 342 (6250) :696-698
[10]  
HUA C, 1986, J IMMUNOL, V136, P1927