POSITIVE AND NEGATIVE SELECTION OF TCRB-V6+ T-CELLS

被引:19
作者
TOMONARI, K
FAIRCHILD, S
机构
[1] Transplantation Biology Section, MRC Clinical Research Centre, Middlesex, HA1 3UJ, Watford Road, Harrow
关键词
D O I
10.1007/BF00215053
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Tcrb-V6+ T cells are deleted by an endogenous superantigen probably encoded by a mouse mammary tumor provirus (Mtv), Mtv-7, in association with major histocompatibility complex (MHC) class II molecules. In contrast, Tcrb-V6+CD4+ T cells are positively selected by MHC class II E molecules in Mtv-7- mice. We have examined the levels of Tcrb-V6+CD4+ and Tcrb-V6+CD8+ T cells from six combinations of backcross mice. In this paper we show that: 1) Tcrb-V6+CD8+ T cells can be positively selected by MHC class I molecules; 2) MHC class Il A molecules can also influence the levels of Tcrb-V6+CD4+ T cells; 3) Mtv-7- NZW mice have a new Mtv, Mtv-44, which cosegregates with a gene encoding the partial deletion ligand for Tcrb-V6+ T cells; 4) the remaining Tcrb-V6+ T cells from mice with partial deletion of these T cells appear not to be anergized in the periphery.
引用
收藏
页码:230 / 237
页数:8
相关论文
共 33 条
[11]   THE ANTIGEN-SPECIFIC, MAJOR HISTOCOMPATIBILITY COMPLEX-RESTRICTED RECEPTOR ON T-CELLS .6. AN ANTIBODY TO A RECEPTOR ALLOTYPE [J].
HASKINS, K ;
HANNUM, C ;
WHITE, J ;
ROEHM, N ;
KUBO, R ;
KAPPLER, J ;
MARRACK, P .
JOURNAL OF EXPERIMENTAL MEDICINE, 1984, 160 (02) :452-471
[12]   SELF-TOLERANCE ELIMINATES T-CELLS SPECIFIC FOR MLS-MODIFIED PRODUCTS OF THE MAJOR HISTOCOMPATIBILITY COMPLEX [J].
KAPPLER, JW ;
STAERZ, U ;
WHITE, J ;
MARRACK, PC .
NATURE, 1988, 332 (6159) :35-40
[13]   POSITIVE SELECTION DETERMINES T-CELL RECEPTOR V-BETA-14 GENE USAGE BY CD8+ T-CELLS [J].
LIAO, NS ;
MALTZMAN, J ;
RAULET, DH .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 170 (01) :135-143
[14]   POSITIVE SELECTION OF CD4+ THYMOCYTES CONTROLLED BY MHC CLASS-II GENE-PRODUCTS [J].
MACDONALD, HR ;
LEES, RK ;
SCHNEIDER, R ;
ZINKERNAGEL, RM ;
HENGARTNER, H .
NATURE, 1988, 336 (6198) :471-473
[15]   T-CELL RECEPTOR V-BETA USE PREDICTS REACTIVITY AND TOLERANCE TO MLSA-ENCODED ANTIGENS [J].
MACDONALD, HR ;
SCHNEIDER, R ;
LEES, RK ;
HOWE, RC ;
ACHAORBEA, H ;
FESTENSTEIN, H ;
ZINKERNAGEL, RM ;
HENGARTNER, H .
NATURE, 1988, 332 (6159) :40-45
[16]  
Maniatis T., 1982, MOL CLONING
[17]  
OZATO K, 1981, J IMMUNOL, V126, P317
[18]  
OZATO K, 1980, J IMMUNOL, V124, P533
[19]   LOWER RECEPTOR AVIDITY REQUIRED FOR THYMIC CLONAL DELETION THAN FOR EFFECTOR T-CELL FUNCTION [J].
PIRCHER, H ;
ROHRER, UH ;
MOSKOPHIDIS, D ;
ZINKERNAGEL, RM ;
HENGARTNER, H .
NATURE, 1991, 351 (6326) :482-485
[20]   THE OPEN READING FRAMES IN THE 3' LONG TERMINAL REPEATS OF SEVERAL MOUSE MAMMARY-TUMOR VIRUS INTEGRANTS ENCODE V-BETA-3-SPECIFIC SUPERANTIGENS [J].
PULLEN, AM ;
CHOI, YW ;
KUSHNIR, E ;
KAPPLER, J ;
MARRACK, P .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 175 (01) :41-47