CROSS-LINKING OF OX40 LIGAND, A MEMBER OF THE TNF/NGF CYTOKINE FAMILY, INDUCES PROLIFERATION AND DIFFERENTIATION IN MURINE SPLENIC B-CELLS

被引:355
作者
STUBER, E [1 ]
NEURATH, M [1 ]
CALDERHEAD, D [1 ]
FELL, HF [1 ]
STROBER, W [1 ]
机构
[1] BRISTOL MYERS SQUIBB PHARMACEUT RES INST,DEPT MOLEC IMMUNOL,SEATTLE,WA 98121
关键词
D O I
10.1016/1074-7613(95)90031-4
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
OX40 is a member of the TNF/NGF-receptor family expressed on activated T cells, whose ligand is found on activated T and a cells. in the present study, we show that cross-linking of OX40L on CD40L-stimulated B cells, alpha lgD dextran-stimulated B cells, or both results in a significantly enhanced proliferative response with no change in the cell survival rate. Furthermore, OX40 stimulation increases immunoglobulin heavy chain mRNA levels and immunoglobulin secretion, which could not be blocked by anti-cytokine antibodies. In additional molecular studies, we show that OX40L cross-linking results in the down-regulation of the transcription factor BSAP. This, in turn, leads to a change in the in vivo binding pattern of the immuno-globulin heavy chain gene 3' alpha enhancer, suggesting its activation. This effect may thus be one mechanism for OX40-induced increase in immunoglobulin secretion. in conclusion, our data suggest that the OX40-OX40L interaction is a novel pathway in T cell-dependent B cell proliferation and differentiation.
引用
收藏
页码:507 / 521
页数:15
相关论文
共 49 条
[21]   INSITU STUDIES OF THE ANTIGEN-DRIVEN SOMATIC HYPERMUTATION OF IMMUNOGLOBULIN GENES [J].
JACOB, J ;
MILLER, C ;
KELSOE, G .
IMMUNOLOGY AND CELL BIOLOGY, 1992, 70 :145-152
[22]   INSITU STUDIES OF THE PRIMARY IMMUNE-RESPONSE TO (4-HYDROXY-3-NITROPHENYL)ACETYL .1. THE ARCHITECTURE AND DYNAMICS OF RESPONDING CELL-POPULATIONS [J].
JACOB, J ;
KASSIR, R ;
KELSOE, G .
JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 173 (05) :1165-1175
[23]   STRUCTURE OF TUMOR NECROSIS FACTOR [J].
JONES, EY ;
STUART, DI ;
WALKER, NPC .
NATURE, 1989, 338 (6212) :225-228
[24]   SITES OF B-CELL ACTIVATION INVIVO [J].
KELSOE, G ;
ZHENG, B .
CURRENT OPINION IN IMMUNOLOGY, 1993, 5 (03) :418-422
[25]   THE PROMOTER OF THE CD19 GENE IS A TARGET FOR THE B-CELL-SPECIFIC TRANSCRIPTION FACTOR BSAP [J].
KOZMIK, Z ;
WANG, S ;
DORFLER, P ;
ADAMS, B ;
BUSSLINGER, M .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (06) :2662-2672
[26]   HIGH-LEVEL PRODUCTION OF MURINE INTERLEUKIN-5 (IL-5) UTILIZING RECOMBINANT BACULOVIRUS EXPRESSION - PURIFICATION OF THE RIL-5 AND ITS USE IN ASSESSING THE BIOLOGIC ROLE OF IL-5 GLYCOSYLATION [J].
KUNIMOTO, DY ;
ALLISON, KC ;
WATSON, C ;
FUERST, T ;
ARMSTRONG, GD ;
PAUL, W ;
STROBER, W .
CYTOKINE, 1991, 3 (03) :224-230
[27]   ACTIVATED HUMAN T-CELLS EXPRESS A LIGAND FOR THE HUMAN-B CELL-ASSOCIATED ANTIGEN CD40 WHICH PARTICIPATES IN T-CELL-DEPENDENT ACTIVATION OF LYMPHOCYTES-B [J].
LANE, P ;
TRAUNECKER, A ;
HUBELE, S ;
INUI, S ;
LANZAVECCHIA, A ;
GRAY, D .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1992, 22 (10) :2573-2578
[28]   SOLUBLE CD40 LIGAND CAN REPLACE THE NORMAL T-CELL-DERIVED CD40 LIGAND SIGNAL TO B-CELLS IN T-CELL-DEPENDENT ACTIVATION [J].
LANE, P ;
BROCKER, T ;
HUBELE, S ;
PADOVAN, E ;
LANZAVECCHIA, A ;
MCCONNELL, F .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 177 (04) :1209-1213
[29]   THE HUMAN OX40 HOMOLOG - CDNA STRUCTURE, EXPRESSION AND CHROMOSOMAL ASSIGNMENT OF THE ACT35 ANTIGEN [J].
LATZA, U ;
DURKOP, H ;
SCHNITTGER, S ;
RINGELING, J ;
EITELBACH, F ;
HUMMEL, M ;
FONATSCH, C ;
STEIN, H .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1994, 24 (03) :677-683