INSIDE THE THYMUS, MLS ANTIGEN IS EXCLUSIVELY PRESENTED BY LYMPHOCYTES-B

被引:13
作者
FARO, J
MARCOS, MAR
ANDREU, JL
MARTINEZ, C
COUTINHO, A
机构
[1] INST PASTEUR, UNITE IMMUNOBIOL, F-75724 PARIS 15, FRANCE
[2] UNIV AUTONOMA MADRID, CTR BIOL MOLEC, CSIC, E-28049 MADRID, SPAIN
[3] CNRS, URA 359, F-75005 PARIS, FRANCE
来源
RESEARCH IN IMMUNOLOGY | 1990年 / 141卷 / 08期
关键词
MIXED LYMPHOCYTE REACTION; THYMUS; MLS ANTIGEN; LYMPHOCYTE-B; MOUSE; PERITONEUM; SPLEEN; APC;
D O I
10.1016/0923-2494(90)90003-H
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 ability to stimulate an Mls-1 mixed lymphocyte reaction (MLR) is predominantly expressed by low density B lymphocytes in the spleen and peritoneal cavity of normal adult mice, and is absent in splenic B cells 1 month after lethal irradiation and reconstitution from autologous bone marrow. Coreconstitution of these mice with normal syngeneic peritoneal cells restores the stimulatory potential of splenic B cells, but sorted CD5 + or CD5 - IgM+ lymphocytes from peritoneum are equally good stimulators, suggesting that functional Mls-1 expression may require long life spans and selection. Bone-marrow-reconstituted DBA/2 mice that fail to express Mls-1 antigens in the periphery nevertheless maintain T-cell receptor V-beta-6 and 8.1 deletions among the newly formed T cells. These findings led us to directly investigate the Mls stimulatory ability of purified antigen-presenting cell populations inside the thymus. We report here that thymic B lymphocytes seem to represent the only intrathymic cell population able to stimulate Mls-1 MLR.
引用
收藏
页码:723 / 737
页数:15
相关论文
共 38 条
[1]   CYTO-TOXIC T-CELL CLONE-SPECIFIC MONOCLONAL-ANTIBODIES USED TO SELECT CLONOTYPIC ANTIGEN-SPECIFIC CYTO-TOXIC T-CELLS [J].
ACHAORBEA, H ;
ZINKERNAGEL, RM ;
HENGARTNER, H .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1985, 15 (01) :31-36
[2]   STUDIES ON NON-H-2-LINKED LYMPHOCYTE-ACTIVATING DETERMINANTS .4. ONTOGENY OF MLS PRODUCT ON MURINE B CELLS [J].
AHMED, A ;
SCHER, I ;
SELL, KW .
CELLULAR IMMUNOLOGY, 1977, 30 (01) :122-134
[3]  
AHMED A, 1976, J IMMUNOL, V117, P1922
[4]   ONTOGENIC CHARACTERIZATION OF THYMIC-B LYMPHOCYTES - ANALYSIS IN DIFFERENT MOUSE STRAINS [J].
ANDREUSANCHEZ, JL ;
FARO, J ;
ALONSO, JM ;
PAIGE, CJ ;
MARTINEZ, C ;
MARCOS, MAR .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1990, 20 (08) :1767-1773
[5]   THE MHC MOLECULE I-E IS NECESSARY BUT NOT SUFFICIENT FOR THE CLONAL DELETION OF V-BETA-11-BEARING T-CELLS [J].
BILL, J ;
KANAGAWA, O ;
WOODLAND, DL ;
PALMER, E .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 169 (04) :1405-1419
[6]   EXPRESSION OF M LOCUS DIFFERENCES BY B CELLS BUT NOT T-CELLS [J].
BOEHMER, HV ;
SPRENT, J .
NATURE, 1974, 249 (5455) :363-365
[7]  
BRUCE J, 1981, J IMMUNOL, V127, P2496
[8]  
CAZENAVE PA, 1989, J IMMUNOL, V142, P8
[9]   TOLERIZE ONE, TOLERIZE THEM ALL - TOLERANCE IS SELF-ASSERTION [J].
COUTINHO, A ;
BANDEIRA, A .
IMMUNOLOGY TODAY, 1989, 10 (08) :264-266
[10]   FINE-TUNING OF MHC CLASS-II GENE-EXPRESSION IN DEFINED MICROENVIRONMENTS [J].
FEHLING, HJ ;
VIVILLE, S ;
VANEWIJK, W ;
BENOIST, C ;
MATHIS, D .
TRENDS IN GENETICS, 1989, 5 (10) :342-347