Modulation of TNF-α mRNA production in rat C6 glioma cells by TNF-α, IL-1β, IL-6, and IFN-α:: In vitro analysis of cytokine-cytokine interactions

被引:23
作者
Gayle, D
Ilyin, SE
Miele, ME
Plata-Salamán, CR [1 ]
机构
[1] Univ Delaware, Sch Life & Hlth Sci, Div Mol Biol, Newark, DE 19716 USA
[2] Univ Delaware, Sch Life & Hlth Sci, Dept Med Technol, Newark, DE 19716 USA
基金
美国国家卫生研究院;
关键词
interleukin; tumor necrosis factor; interferon; growth factor; nervous system; brain cell; RNase protection;
D O I
10.1016/S0361-9230(98)00078-1
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Cytokines regulate the expression of other cytokines in the centrally derived rat C6 glioma cell line. However, the modulation of tumor necrosis factor-alpha (TNF-alpha, a pivotal proinflammatory cytokine) in C6 cells is unknown. Here we investigated the expression of TNF-alpha mRNA in C6 glioma cells in response to TNF-alpha, interleukin-1 beta (IL-1 beta), IL-1 receptor antagonist (IL-1Ra), interleukin-6 (IL-6), and interferon-alpha (IFN-alpha), The data show that (1) IL-1 beta induced a significant upregulation of TNF-LU mRNA; (2) the effect of IL-1 beta on TNF-alpha mRNA expression was completely blocked by the concomitant application of IL-1Ra, which suggests specificity of IL-1 beta action through the IL-l signaling receptor; (3) no detectable modulation of TNF-alpha mRNA expression was observed with the individual applications of TNF-alpha, IL-6, or IFN-alpha; (4) the concomitant treatments of TNF-alpha + IL-1 beta or TNF-alpha + IL-1 beta + IL-6 strongly upregulated TNF-alpha mRNA expression, whereas the concomitant application of TNF-alpha + IL-6 or IL-1 beta + IL-6 induced a moderate increase; and (5) IFN-alpha significantly attenuated induction of TNF-alpha mRNA by TNF-alpha + IL-1 beta + IL-6. Thus, IL-1 beta, TNF-alpha and IL-6 interact to upregulate TNF-alpha mRNA expression synergistically, and IFN-alpha acts as an inhibitory cytokine in C6 glioma cells. These findings also suggest that the rat C6 glioma cell line may be used as an in vitro model to characterize cytokine-cytokine interactions. (C) 1998 Elsevier Science Inc.
引用
收藏
页码:231 / 235
页数:5
相关论文
共 33 条
[1]   INTERFERON-ALPHA DOWN-REGULATES THE INTERLEUKIN-6 RECEPTOR IN A HUMAN MULTIPLE-MYELOMA CELL-LINE, U266 [J].
ANTHES, JC ;
ZHAN, ZR ;
GILCHREST, H ;
EGAN, RW ;
SIEGEL, MI ;
BILLAH, MM .
BIOCHEMICAL JOURNAL, 1995, 309 :175-180
[2]   EXPRESSION OF INTERLEUKIN-3 AND TUMOR NECROSIS FACTOR-BETA MESSENGER-RNAS IN CULTURED MICROGLIA [J].
APPEL, K ;
HONEGGER, P ;
GEBICKEHAERTER, PJ .
JOURNAL OF NEUROIMMUNOLOGY, 1995, 60 (1-2) :83-91
[3]   Nuclear factor kappa B [J].
Barnes, PJ .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 1997, 29 (06) :867-870
[4]   The role of nuclear factor-kappa B in cytokine gene regulation [J].
Blackwell, TS ;
Christman, JW .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1997, 17 (01) :3-9
[5]   The Tat protein of HIV-1 induces tumor necrosis factor-alpha production - Implications for HIV-1-associated neurological diseases [J].
Chen, PQ ;
Mayne, M ;
Power, C ;
Nath, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (36) :22385-22388
[6]   REGULATION OF TUMOR NECROSIS FACTOR-ALPHA TRANSCRIPTION IN MACROPHAGES - INVOLVEMENT OF 4 KAPPA-B-LIKE MOTIFS AND OF CONSTITUTIVE AND INDUCIBLE FORMS OF NF-KAPPA-B [J].
COLLART, MA ;
BAEUERLE, P ;
VASSALLI, P .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (04) :1498-1506
[7]   Biologic basis for interleukin-1 in disease [J].
Dinarello, CA .
BLOOD, 1996, 87 (06) :2095-2147
[8]  
Dobashi K, 1997, J NEUROCHEM, V68, P1896
[9]  
Drescher KM, 1996, INVEST OPHTH VIS SCI, V37, P2302