COMPARISON OF THE INDUCTION OF CYCLOOXYGENASE AND NITRIC-OXIDE SYNTHASE BY ENDOTOXIN IN ENDOTHELIAL-CELLS AND MACROPHAGES

被引:82
作者
AKARASEREENONT, P [1 ]
MITCHELL, JA [1 ]
BAKHLE, YS [1 ]
THIEMERMANN, C [1 ]
VANE, JR [1 ]
机构
[1] UNIV LONDON ST BARTHOLOMEWS HOSP & MED COLL,WILLIAM HARVEY RES INST,LONDON EC1M 6BQ,ENGLAND
关键词
CYTOKINE; LIPOPOLYSACCHARIDE; MITOGEN; NITRIC OXIDE (NO); PROSTAGLANDIN;
D O I
10.1016/0014-2999(94)00680-6
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Endotoxin causes the expression of inducible nitric oxide (NO) synthase and cyclooxygenase-2. We have compared the ability of endotoxin to increase the activities of these enzymes in bovine aortic endothelial cells and the macrophage cell line (J774.2). Endotoxin (1 mu g ml(-1); for 24 h) caused a time-dependent increase in the accumulation of cyclooxygenase metabolites from endogenous arachidonic acid, in both cell types. Cyclooxygenase activity towards exogenous arachidonic acid (30 mu M; for 15 min) was also increased in both cell types. Endothelial cells and macrophages also contained comparable amounts of cyclooxygenase-2 protein after incubation with endotoxin for 24 h which was prevented by pretreatment with cycloheximide (10 mu g ml(-1); 30 min prior to endotoxin). Endotoxin for 24 h caused a time-dependent increase in nitrite accumulation in macrophages, but not in endothelial cells. Thus, endotoxin increased cyclooxygenase activity and induced cyclooxygenase-2 protein in endothelial cells and macrophages. Endotoxin also increased NO synthase activity in macrophages, but not in endothelial cells.
引用
收藏
页码:121 / 128
页数:8
相关论文
共 40 条
[1]  
AKARASEREENONT P, 1994, BRIT J PHARMACOL, V111, pP33
[2]   SELECTIVE-INHIBITION BY DEXAMETHASONE OF INDUCTION OF NO SYNTHASE, BUT NOT OF INDUCTION OF L-ARGININE TRANSPORT, IN ACTIVATED MURINE MACROPHAGE J774 CELLS [J].
BAYDOUN, AR ;
BOGLE, RG ;
PEARSON, JD ;
MANN, GE .
BRITISH JOURNAL OF PHARMACOLOGY, 1993, 110 (04) :1401-1406
[3]   ENDOTOXIN-INDUCED ARTERIAL ENDOTHELIAL BARRIER DYSFUNCTION ASSESSED BY AN IN-VITRO MODEL [J].
BERMAN, RS ;
FREW, JD ;
MARTIN, W .
BRITISH JOURNAL OF PHARMACOLOGY, 1993, 110 (04) :1282-1284
[4]   GROWTH-FACTORS IN DEVELOPMENT, TRANSFORMATION, AND TUMORIGENESIS [J].
CROSS, M ;
DEXTER, TM .
CELL, 1991, 64 (02) :271-280
[5]  
DENUCCI G, 1988, P NATL ACAD SCI USA, V85, P2334
[6]   GLUCOCORTICOIDS INHIBIT THE INDUCTION OF NITRIC-OXIDE SYNTHASE IN MACROPHAGES [J].
DIROSA, M ;
RADOMSKI, M ;
CARNUCCIO, R ;
MONCADA, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 172 (03) :1246-1252
[7]   PHOSPHOLIPASE-A2 ENZYMES - REGULATION AND INHIBITION [J].
GLASER, KB ;
MOBILIO, D ;
CHANG, JY ;
SENKO, N .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1993, 14 (03) :92-98
[8]   CYTOKINE-ACTIVATED ENDOTHELIAL-CELLS EXPRESS AN ISOTYPE OF NITRIC-OXIDE SYNTHASE WHICH IS TETRAHYDROBIOPTERIN-DEPENDENT, CALMODULIN-INDEPENDENT AND INHIBITED BY ARGININE ANALOGS WITH A RANK-ORDER OF POTENCY CHARACTERISTIC OF ACTIVATED MACROPHAGES [J].
GROSS, SS ;
JAFFE, EA ;
LEVI, R ;
KILBOURN, RG .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 178 (03) :823-829
[9]  
GROSS SS, 1992, J BIOL CHEM, V267, P25722
[10]   BIOASSAY OF PROSTACYCLIN AND ENDOTHELIUM-DERIVED RELAXING FACTOR (EDRF) FROM PORCINE AORTIC ENDOTHELIAL-CELLS [J].
GRYGLEWSKI, RJ ;
MONCADA, S ;
PALMER, RMJ .
BRITISH JOURNAL OF PHARMACOLOGY, 1986, 87 (04) :685-694