MULTIPLE CYTOKINE INTERACTIONS REGULATE LY-6E ANTIGEN EXPRESSION - COOPERATIVE LY-6E INDUCTION BY IFNS, TNF, AND IL-1 IN A T-CELL LYMPHOMA AND IN ITS INDUCTION-DEFICIENT VARIANTS

被引:7
作者
ALTMEYER, A
STARUCH, MJ
COFANO, F
LANDOLFO, S
DUMONT, FJ
机构
[1] MERCK SHARP & DOHME RES INST,DEPT IMMUNOL,POB 2000,RAHWAY,NJ 07065
[2] UNIV TURIN,INST MICROBIOL,I-10124 TURIN,ITALY
关键词
D O I
10.1016/0008-8749(91)90135-X
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The cell surface Ly-6E antigen, known to play a role in T cell activation, is up-regulated by IFNs. In the present study, we investigated the possible interactions between IFNs and other cytokines in this regulation. As a model system, we used the YAC T cell lymphoma, in which Ly-6E is normally absent but can be highly induced both at the mRNA and surface protein levels by IFN-γ or IFN- α β. The combination of the two IFNs was found to result in markedly synergistic Ly-6E induction in this cell line. Moreover, mutants of YAC cells were isolated that did not respond to the Ly-6E-inducing action of IFN-γ or IFN- α β alone but did respond to their combination. Such a synergistic interaction is consistent with the notion that the two IFN types utilize different intracellular mechanisms to induce Ly-6E expression. Ly-6E induction mediated by IFN-γ or IFN- α β was also enhanced by cotreatment with TNF-α or IL-1α, which by themselves had no detectable Ly-6E-inducing effect. These two cytokines similarly synergized with IFNs to trigger a response in several Ly-6E-induction-deficient mutants. However, their action could be dissociated in one mutant (B54) where the response to IFN- α β was enhanced by TNF-α, but not by IL-1α. Altogether, these data indicate that Ly-6E antigen expression is regulated by the interaction of several inflammatory cytokines, which may provide a mechanism for the local modulation of T cell activation. The YAC cell mutants described here should facilitate further analysis of the molecular bases of Ly-6E regulation. © 1991.
引用
收藏
页码:94 / 107
页数:14
相关论文
共 47 条
[1]   EVIDENCE THAT TYPE-I AND TYPE-II INTERFERONS HAVE DIFFERENT RECEPTORS [J].
BRANCA, AA ;
BAGLIONI, C .
NATURE, 1981, 294 (5843) :768-770
[2]  
CHANG RJ, 1986, J IMMUNOL, V137, P2853
[3]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[4]  
CODIAS EK, 1990, J IMMUNOL, V145, P1407
[5]   BINDING OF MURINE I-125 LABELED NATURAL INTERFERON-GAMMA TO MURINE CELL RECEPTORS [J].
COFANO, F ;
FASSIO, A ;
CAVALLO, G ;
LANDOLFO, S .
JOURNAL OF GENERAL VIROLOGY, 1986, 67 :1205-1209
[6]   MOLECULAR-CLONING OF MURINE INTERFERON GAMMA (MUIFN-GAMMA) CDNA AND ITS EXPRESSION IN HETEROLOGOUS MAMMALIAN-CELLS [J].
DIJKMANS, R ;
VOLCKAERT, G ;
VANDAMME, J ;
DELEY, M ;
BILLIAU, A ;
DESOMER, P .
JOURNAL OF INTERFERON RESEARCH, 1985, 5 (03) :511-520
[7]  
DOMONT FJ, 1991, CELL IMMUNOL, V132, P466
[8]   BIOCHEMISTRY OF MUTAGENESIS [J].
DRAKE, JW ;
BALTZ, RH .
ANNUAL REVIEW OF BIOCHEMISTRY, 1976, 45 :11-37
[9]   AN INTERFERON GAMMA-REGULATED PROTEIN THAT BINDS THE INTERFERON-INDUCIBLE ENHANCER ELEMENT OF MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-I GENES [J].
DRIGGERS, PH ;
ENNIST, DL ;
GLEASON, SL ;
MAK, WH ;
MARKS, MS ;
LEVI, BZ ;
FLANAGAN, JR ;
APPELLA, E ;
OZATO, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (10) :3743-3747
[10]  
DUMONT FJ, 1987, J IMMUNOL, V139, P4088