Inhibition of inducible nitric oxide synthase gene expression by glucocorticoid-induced protein(s) in lipopolysaccharide-stimulated J774 cells

被引:11
作者
D'Acquisto, F
Cicatiello, L
Iuvone, T
Ialenti, A
Ianaro, A
Esumi, H
Weisz, A
Carnuccio, R
机构
[1] Univ Naples Federico II, Dept Expt Pharmacol, I-80131 Naples, Italy
[2] Univ Naples 2, Inst Gen Pathol & Oncol, Naples, Italy
[3] Natl Canc Ctr, Res Inst E, Invest Canc Treatment Div, Chiba, Japan
关键词
glucocorticoid; nitric oxide (NO); nitric oxide (NO) synthase; inducible; lipocortin; J774; macrophage; lipopolysaccharide;
D O I
10.1016/S0014-2999(97)01361-7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Glucocorticoids inhibit inducible-type NO synthase activity in a Variety of cell types. We report here that proteins recovered from the medium of dexamethasone-treated J774 macrophages (1, 10, 100 mu g/ml) inhibited lipopolysaccharide-stimulated nitrite generation by 10.0 +/- 3.0%, 32.3 +/- 5.3% and 55.0 +/- 6.0%, respectively, and inducible NO synthase mRNA expression in these cells. Immunoblotting analysis of crude and partially purified glucocorticoid-induced proteins with an anti-lipocortin-1 polyclonal antiserum revealed the presence of lipocortin-1-like immunoreactive species with a molecular mass of 35-37 kDa. Furthermore, inhibition of lipopolysaccharide-induced nitrite production by glucocorticoid-induced proteins in J774 cells was reversed by addition of anti-lipocortin-1 neutralizing polyclonal antibody (1:60 dilution; 4 h before lipopolysaccharide). Comparison of glucocorticoid-induced proteins inhibition of both nitrite production and inducible NO synthase mRNA expression suggests that these effects result mainly from inhibition of lipopolysaccharide-mediated inducible NO synthase gene expression. These results indicate that negative regulation of inducible NO synthase by glucocorticoids is, at least in part, mediated by glucocorticoid-induced proteins that involve also members of the lipocortin-like superfamily. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:87 / 95
页数:9
相关论文
共 24 条
[1]   MOLECULAR-CLONING OF A CDNA-ENCODING AN INDUCIBLE CALMODULIN-DEPENDENT NITRIC-OXIDE SYNTHASE FROM RAT-LIVER AND ITS EXPRESSION IN COS-1 CELLS [J].
ADACHI, H ;
IIDA, S ;
OGUCHI, S ;
OHSHIMA, H ;
SUZUKI, H ;
NAGASAKI, K ;
KAWASAKI, H ;
SUGIMURA, T ;
ESUMI, H .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1993, 217 (01) :37-43
[2]  
COHEN JJ, 1989, ANTIINFLAMMATORY STE, P111
[3]   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
[4]   LIPOCORTIN-1 - CELLULAR MECHANISMS AND CLINICAL RELEVANCE [J].
FLOWER, RJ ;
ROTHWELL, NJ .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1994, 15 (03) :71-76
[6]   ANALYSIS OF NITRATE, NITRITE, AND [N-15]-LABELED NITRATE IN BIOLOGICAL-FLUIDS [J].
GREEN, LC ;
WAGNER, DA ;
GLOGOWSKI, J ;
SKIPPER, PL ;
WISHNOK, JS ;
TANNENBAUM, SR .
ANALYTICAL BIOCHEMISTRY, 1982, 126 (01) :131-138
[7]   NG-METHYL-L-ARGININE INHIBITS TUMOR NECROSIS FACTOR-INDUCED HYPOTENSION - IMPLICATIONS FOR THE INVOLVEMENT OF NITRIC-OXIDE [J].
KILBOURN, RG ;
GROSS, SS ;
JUBRAN, A ;
ADAMS, J ;
GRIFFITH, OW ;
LEVI, R ;
LODATO, RF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (09) :3629-3632
[8]   NITRIC-OXIDE SYNTHASES IN MAMMALS [J].
KNOWLES, RG ;
MONCADA, S .
BIOCHEMICAL JOURNAL, 1994, 298 :249-258
[9]   LIPOPOLYSACCHARIDE TREATMENT IN-VIVO INDUCES WIDESPREAD TISSUE EXPRESSION OF INDUCIBLE NITRIC-OXIDE SYNTHASE MESSENGER-RNA [J].
LIU, SF ;
ADCOCK, IM ;
OLD, RW ;
BARNES, PJ ;
EVANS, TW .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 196 (03) :1208-1213
[10]   CLONING OF CDNA SEQUENCES OF HORMONE-REGULATED GENES FROM THE MCF-7 HUMAN-BREAST CANCER CELL-LINE [J].
MASIAKOWSKI, P ;
BREATHNACH, R ;
BLOCH, J ;
GANNON, F ;
KRUST, A ;
CHAMBON, P .
NUCLEIC ACIDS RESEARCH, 1982, 10 (24) :7895-7963