Generation of inflammatory cytokines in zymosan-induced pleurisy in rats: TNF induces IL-6 and cytokine-induced neutrophil chemoattractant (CINC) in vivo

被引:47
作者
Utsunomiya, I [1 ]
Ito, M [1 ]
Oh-ishi, S [1 ]
机构
[1] Kitasato Univ, Sch Pharmaceut Sci, Dept Pharmacol, Minato Ku, Tokyo 108, Japan
关键词
cytokines; neutrophils; pleurisy; T-kininogen; CINC;
D O I
10.1006/cyto.1998.0376
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
Levels of inflammatory cytokines tumour necrosis factor (TNF), interleukin 1 (LL-l), IL-6, and cytokine-induced neutrophil chemoattractant (CINC), which is a member of the alpha-chemokine family in rats, were measured in the pleural exudates during zymosan-induced pleurisy to examine the relationship between the local production of cytokines and the inflammatory reaction. All four cytokine levels in the pleural exudate began to increase after 1-2 h, preceding the influx of neutrophils, and peaked after 4-5 h, Thereafter, these cytokine levels declined after 24 h, whereas the exudate volume still continued to increase and leukocyte number reached a plateau, Concomitant injection of actinomycin D (10 mu g) with zymosan markedly suppressed the neutrophil infiltration, parallel with CINC production in the pleural exudate at 4 h, A transient elevation of IL-6 level, peaking at 5 h, and subsequent rise in the level of an acute-phase protein, T-kininogen, were also observed in the plasma. When recombinant human TNF-alpha (rhTNF-alpha) (20 000 U) was intrapleurally injected a rapid increase in pleural: CINC level, followed by neutrophil infiltration, and a sharp rise in IL-6 level in the plasma, followed by an increase in T-kininogen, were demonstrated. These results suggest that CINC produced in the pleural exudate may participate in neutrophil infiltration, that IL-6 induced in the plasma stimulates T-kininogen production, and that endogenous TNF may be partly involved in the induction of CINC and IL-6 in this zymosan inflammation. (C) 1998 Academic Press.
引用
收藏
页码:956 / 963
页数:8
相关论文
共 43 条
[21]   ESTABLISHMENT OF AN INTERLEUKIN 6 (IL 6)/B-CELL STIMULATORY FACTOR 2-DEPENDENT CELL-LINE AND PREPARATION OF ANTI-IL-6 MONOCLONAL-ANTIBODIES [J].
MATSUDA, T ;
HIRANO, T ;
KISHIMOTO, T .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1988, 18 (06) :951-956
[22]   MOLECULAR-CLONING OF A HUMAN MONOCYTE-DERIVED NEUTROPHIL CHEMOTACTIC FACTOR (MDNCF) AND THE INDUCTION OF MDNCF MESSENGER-RNA BY INTERLEUKIN-1 AND TUMOR NECROSIS FACTOR [J].
MATSUSHIMA, K ;
MORISHITA, K ;
YOSHIMURA, T ;
LAVU, S ;
KOBAYASHI, Y ;
LEW, W ;
APPELLA, E ;
KUNG, HF ;
LEONARD, EJ ;
OPPENHEIM, JJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 167 (06) :1883-1893
[23]  
MIZEL SB, 1978, J IMMUNOL, V120, P1497
[24]  
MOVAT HZ, 1985, INFLAMMATORY REACTIO, P77
[25]  
MULLIGAN MS, 1992, J IMMUNOL, V149, P331
[26]   MOLECULAR-CLONING AND EXPRESSION OF RAT INTERLEUKIN-1-ALPHA CDNA [J].
NISHIDA, T ;
NISHINO, N ;
TAKANO, M ;
SEKIGUCHI, Y ;
KAWAI, K ;
MIZUNO, K ;
NAKAI, S ;
MASUI, Y ;
HIRAI, Y .
JOURNAL OF BIOCHEMISTRY, 1989, 105 (03) :351-357
[27]   ISOLATION AND STRUCTURE OF T-KININ [J].
OKAMOTO, H ;
GREENBAUM, LM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1983, 112 (02) :701-708
[28]   PROPERTIES OF THE NOVEL PROINFLAMMATORY SUPERGENE INTERCRINE CYTOKINE FAMILY [J].
OPPENHEIM, JJ ;
ZACHARIAE, COC ;
MUKAIDA, N ;
MATSUSHIMA, K .
ANNUAL REVIEW OF IMMUNOLOGY, 1991, 9 :617-648
[29]   REQUIREMENT OF TUMOR-NECROSIS-FACTOR FOR DEVELOPMENT OF SILICA-INDUCED PULMONARY FIBROSIS [J].
PIGUET, PF ;
COLLART, MA ;
GRAU, GE ;
SAPPINO, AP ;
VASSALLI, P .
NATURE, 1990, 344 (6263) :245-247
[30]   PREVENTION OF LUNG REPERFUSION INJURY IN RABBITS BY A MONOCLONAL-ANTIBODY AGAINST INTERLEUKIN-8 [J].
SEKIDO, N ;
MUKAIDA, N ;
HARADA, A ;
NAKANISHI, I ;
WATANABE, Y ;
MATSUSHIMA, K .
NATURE, 1993, 365 (6447) :654-657