Bacterial lipopolysaccharide increases prostaglandin production by rat astrocytes via inducible cyclo-oxygenase:: Evidence for the involvement of nuclear factor κB

被引:40
作者
Pistritto, G
Franzese, O
Pozzoli, G
Mancuso, C
Tringali, G
Preziosi, P
Navarra, P [1 ]
机构
[1] Univ Cattolica Sacro Cuore, Sch Med, Inst Pharmacol, I-00168 Rome, Italy
[2] Univ Roma Tor Vergata, Dept Expt Med & Biochem Sci, Rome, Italy
关键词
lipopolysaccharide; prostaglandin E2; inducible cyclo-oxygenase; nuclear factor kappa B; dexamethasone; aurothiomalate; diethyldithiocarbamate; astrocytes;
D O I
10.1006/bbrc.1999.1413
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
This study was set to investigate the mechanisms through which bacterial lipopolysaccharide (LPS) stimulates prostaglandin (PG) production in rat astrocytes. Primary cultures of rat hypothalamic astrocytes were established. Cells were treated with LPS alone or LPS plus antagonists of various pathways, and the subsequent changes in cyclo-oxygenase (COX) activity were monitored by measuring a COX end product, PGE2, released into the incubation medium. It was found that (i) LPS produced a concentration-dependent increase in PGE2 release from astrocytes. The potency of LPS was significantly increased by the addition of serum into the incubation medium; (ii) after 24 h of incubation, inducible COX (COX-2) accounts for most of the LPS-stimulated PG production, as the latter was markedly reduced by dexamethasone and the specific COX-2 inhibitor NS 398; and (iii) nuclear factor kappa B appears to play a role in the activation of COX-2 induced by LPS, since certain inhibitors of this transcription factor were able to antagonize, at least in part, the effects of LPS on PGE2 release. (C) 1999 Academic Press.
引用
收藏
页码:570 / 574
页数:5
相关论文
共 23 条
[1]   Mechanisms of disease - Nuclear factor-kappa b - A pivotal transcription factor in chronic inflammatory diseases [J].
Barnes, PJ ;
Larin, M .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 336 (15) :1066-1071
[2]  
Boumpas DT, 1996, BRIT J RHEUMATOL, V35, P709
[3]   DISTRIBUTION AND CHARACTERIZATION OF CYCLOOXYGENASE IMMUNOREACTIVITY IN THE OVINE BRAIN [J].
BREDER, CD ;
SMITH, WL ;
RAZ, A ;
MASFERRER, J ;
SEIBERT, K ;
NEEDLEMAN, P ;
SAPER, CB .
JOURNAL OF COMPARATIVE NEUROLOGY, 1992, 322 (03) :409-438
[4]  
BREDER CD, 1995, J COMP NEUROL, V355, P295
[5]   ACCURATE TRANSCRIPTION INITIATION BY RNA POLYMERASE-II IN A SOLUBLE EXTRACT FROM ISOLATED MAMMALIAN NUCLEI [J].
DIGNAM, JD ;
LEBOVITZ, RM ;
ROEDER, RG .
NUCLEIC ACIDS RESEARCH, 1983, 11 (05) :1475-1489
[6]   NS-398, A NEW ANTIINFLAMMATORY AGENT, SELECTIVELY INHIBITS PROSTAGLANDIN-G/H SYNTHASE CYCLOOXYGENASE (COX-2) ACTIVITY IN-VITRO [J].
FUTAKI, N ;
TAKAHASHI, S ;
YOKOYAMA, M ;
ARAI, I ;
HIGUCHI, S ;
OTOMO, S .
PROSTAGLANDINS, 1994, 47 (01) :55-59
[7]   CD14 mediates endotoxin induction of nitric oxide synthase in cultured brain glial cells [J].
Galea, E ;
Reis, DJ ;
Fox, ES ;
Xu, H ;
Feinstein, DL .
JOURNAL OF NEUROIMMUNOLOGY, 1996, 64 (01) :19-28
[8]   Neuroprotection by aspirin and sodium salicylate through blockade of NF-kappa B activation [J].
Grilli, M ;
Pizzi, M ;
Memo, M ;
Spano, P .
SCIENCE, 1996, 274 (5291) :1383-1385
[9]  
HEWETT JA, 1993, PHARMACOL REV, V45, P381
[10]   INTERLEUKIN-1-BETA INCREASES PROSTAGLANDIN-E2 IN RAT ASTROCYTE CULTURES - MODULATORY EFFECT OF NEUROPEPTIDES [J].
KATSUURA, G ;
GOTTSCHALL, PE ;
DAHL, RR ;
ARIMURA, A .
ENDOCRINOLOGY, 1989, 124 (06) :3125-3127