Antibodies to rat soluble IL-6 receptor stimulate B9 hybridoma cell proliferation

被引:4
作者
Thibault, V [1 ]
Richards, CD [1 ]
Botelho, F [1 ]
Gauldie, J [1 ]
机构
[1] MCMASTER UNIV,HLTH SCI CTR,DEPT PATHOL,HAMILTON,ON L8N 3Z5,CANADA
关键词
IL-6; receptor; B9; hybridoma; signalling; STAT;
D O I
10.1016/S0014-5793(97)00417-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Interleukin-6 mediates its pleiotropic effects by interacting with its membrane bound receptor (gp80) or the soluble counterpart gp54, resulting in activation of a complex that includes the transducer protein gp130, We have generated a polyclonal antibody against the rat soluble IL-6 receptor (anti-rat sIL-6R) in rabbits, By Western blot analysis we show that purified anti-rat sIL-6R IgG antibody reacts specifically with recombinant rat sIL-6R generated from E, coli, baculovirus or adenovirus expression systems. Anti-rat sIL-6R inhibited IL-6-induced acute phase protein synthesis in rat (H35) but not human (HepG2) hepatoma cells, and did not affect stimulation of those cells by Oncostatin-M, Conversely, on the mouse hybridoma B9 cell line, IgG anti-rat sIL-6R showed a dose-dependent stimulation of proliferation, Fab fragments of this antibody did not stimulate, but abrogated IL-6-mediated hepatoma cell stimulation and B9 cell proliferation, Gel shift analysis of STAT nuclear factors showed activation of STAT DNA binding in nuclei of B9 cells treated with IgG anti-rat sIL-6R, whereas in H35, NIH-3T3 and M1 cells, only IL-6 could trigger a similar STAT activation. Our data suggest that mechanisms of IL-6 receptor activation and signalling in mouse B9 hybridoma cells show subtle but important differences from other IL-6-responsive cells. (C) 1997 Federation of European Biochemical Societies.
引用
收藏
页码:182 / 186
页数:5
相关论文
共 33 条
  • [11] JAKS AND STATS IN SIGNALING BY THE CYTOKINE RECEPTOR SUPERFAMILY
    IHLE, JN
    KERR, IM
    [J]. TRENDS IN GENETICS, 1995, 11 (02) : 69 - 74
  • [12] Ihle JN, 1995, ADV IMMUNOL, V60, P1, DOI 10.1016/S0065-2776(08)60582-9
  • [13] INTERLEUKIN-6 FAMILY OF CYTOKINES AND GP130
    KISHIMOTO, T
    AKIRA, S
    NARAZAKI, M
    TAGA, T
    [J]. BLOOD, 1995, 86 (04) : 1243 - 1254
  • [14] KISHIMOTO T, 1994, STEM CELLS, V12, P44
  • [15] KUMAR G, 1994, J IMMUNOL, V153, P4436
  • [16] INTERLEUKIN-6-INDUCED SERINE PHOSPHORYLATION OF TRANSCRIPTION FACTOR APRF - EVIDENCE FOR A ROLE IN INTERLEUKIN-6 TARGET GENE INDUCTION
    LUTTICKEN, C
    COFFER, P
    YUAN, JP
    SCHWARTZ, C
    CALDENHOVEN, E
    SCHINDLER, C
    KRUIJER, W
    HEINRICH, PC
    HORN, F
    [J]. FEBS LETTERS, 1995, 360 (02) : 137 - 143
  • [17] ASSOCIATION OF TRANSCRIPTION FACTOR APRF AND PROTEIN-KINASE JAK1 WITH THE INTERLEUKIN-6 SIGNAL TRANSDUCER GP130
    LUTTICKEN, C
    WEGENKA, UM
    YUAN, JP
    BUSCHMANN, J
    SCHINDLER, C
    ZIEMIECKI, A
    HARPUR, AG
    WILKS, AF
    YASUKAWA, K
    TAGA, T
    KISHIMOTO, T
    BARBIERI, G
    PELLEGRINI, S
    SENDTNER, M
    HEINRICH, PC
    HORN, F
    [J]. SCIENCE, 1994, 263 (5143) : 89 - 92
  • [18] MACKIEWICZ A, 1992, J IMMUNOL, V149, P2021
  • [19] MATSUDA T, 1994, BLOOD, V83, P3457
  • [20] Dual oncostatin M (OSM) receptors - Cloning and characterization of an alternative signaling subunit conferring OSM-specific receptor activation
    Mosley, B
    DeImus, C
    Friend, D
    Boiani, N
    Thoma, B
    Park, LS
    Cosman, D
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (51) : 32635 - 32643