Negative regulation of LPS-stimulated expression of inducible nitric oxide synthase by AP-1 in macrophage cell line J774A.1

被引:15
作者
Kizaki, T
Suzuki, K
Hitomi, Y
Iwabuchi, K
Onoé, K
Haga, S
Ishida, H
Ookawara, T
Suzuki, K
Ohno, H
机构
[1] Kyorin Univ, Sch Med, Dept Mol Predict Med & Sport Sci, Tokyo 1818611, Japan
[2] Hokkaido Univ, Inst Med Genet, Res Sect Pathophysiol, Div Immunobiol, Sapporo, Hokkaido, Japan
[3] Univ Tsukuba, Inst Hlth & Sport Sci, Tsukuba, Ibaraki 305, Japan
[4] Kyorin Univ, Sch Med, Dept Internal Med 3, Mitaka, Tokyo 181, Japan
[5] Hyogo Med Univ, Dept Biochem, Nishinomiya, Hyogo 663, Japan
关键词
macrophage; NOSII; negative regulation; AP-1;
D O I
10.1006/bbrc.2001.6123
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
The level of NOS 11 mRNA was markedly increased during 24 h lipopolysaccharide (LPS) stimulation, but showed no further increase thereafter. On the other hand, the level of NOS 11 mRNA in J774A.1 cells transfected with an expression vector containing the rat csk cDNA (J.Csk) was significantly increased during 3 h LPS stimulation, but rather decreased thereafter. Although no significant difference was observed in the activation of NF-kappaB by LPS among parental J774A.1, J774A.1 transfected with promoterless vector (J.pBK), and J.Csk cells, activity of c-Jun N-terminal kinase (JNK) and nuclear translocation of nuclear factor activator protein-1 (AP-1) were markedly upregulated in the J.Csk cells. Then luciferase reporter vectors containing NOS 11 promoter with mutations in two AP-1-like sites (U site, -1126similar to-1120; L site, -524similar to-518) were transiently transfected in J774A.1 cells. The promoter activity following LPS stimulation for 24 h was significantly increased by mutation at the L site, but not by mutation at the U site, suggesting that NOS 11 expression is negatively regulated, at least in part, through the AP-1-like L site in response to LPS. (C) 2001 Elsevier Science.
引用
收藏
页码:1031 / 1038
页数:8
相关论文
共 39 条
[1]   LIPOPOLYSACCHARIDE-INDUCED CYTOKINE PRODUCTION IN HUMAN MONOCYTES - ROLE OF TYROSINE PHOSPHORYLATION IN TRANSMEMBRANE SIGNAL-TRANSDUCTION [J].
BEATY, CD ;
FRANKLIN, TL ;
UEHARA, Y ;
WILSON, CB .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1994, 24 (06) :1278-1284
[2]  
BOULET I, 1992, ONCOGENE, V7, P703
[3]   ONCOGENES AND SIGNAL TRANSDUCTION [J].
CANTLEY, LC ;
AUGER, KR ;
CARPENTER, C ;
DUCKWORTH, B ;
GRAZIANI, A ;
KAPELLER, R ;
SOLTOFF, S .
CELL, 1991, 64 (02) :281-302
[4]  
Chen CC, 1999, MOL PHARMACOL, V55, P481
[5]  
Chen CC, 1998, J IMMUNOL, V161, P6206
[6]   NEGATIVE REGULATION OF T-CELL RECEPTOR SIGNALING BY TYROSINE PROTEIN-KINASE P50(CSK) [J].
CHOW, LML ;
FOURNEL, M ;
DAVIDSON, D ;
VEILLETTE, A .
NATURE, 1993, 365 (6442) :156-160
[7]   Analysis of the cytokine-stimulated human inducible nitric oxide synthase (iNOS) gene: Characterization of differences between human and mouse iNOS promoters [J].
Chu, SC ;
Marks-Konczalik, J ;
Wu, HP ;
Banks, TC ;
Moss, J .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 248 (03) :871-878
[8]   Modulation of immune complex-induced inflammation in vivo by the coordinate expression of activation and inhibitory Fc receptors [J].
Clynes, R ;
Maizes, JS ;
Guinamard, R ;
Ono, M ;
Takai, T ;
Ravetch, JV .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 189 (01) :179-185
[9]   THE WHEN AND HOW OF SRC REGULATION [J].
COOPER, JA ;
HOWELL, B .
CELL, 1993, 73 (06) :1051-1054
[10]  
CORBETT JA, 1991, J BIOL CHEM, V266, P21351