Repression of interferon-γ-induced inducible nitric oxide synthase (iNOS) gene expression in microglia by sodium butyrate is mediated through specific inhibition of ERK signaling pathways

被引:52
作者
Park, JS
Woo, MS
Kim, SY
Kim, WK
Kim, HS
机构
[1] Ewha Womans Univ, Sch Med, Ewha Inst Neurosci, Dept Neurosci, Seoul 110783, South Korea
[2] Ewha Womans Univ, Sch Med, Ewha Inst Neurosci, Dept Pharmacol, Seoul, South Korea
关键词
microglia; sodium butyrate; iNOS; ERK; NF-kappa B; IRF-1;
D O I
10.1016/j.jneuroim.2005.07.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We have reported recently that sodium butyrate suppressed IFN-gamma, but not the LPS-mediated induction of nitric oxide and TNF-alpha in microglia via the specific inhibition of NF-kappa B. In order to further determine the upstream signaling mechanism involved in the IFN-gamma-specific down-regulation of iNOS by sodium butyrate in microglia, this study investigated the effect of sodium butyrate on the MAP kinase activities, Sodium butyrate significantly repressed the phosphorylation of ERK induced by IFN-gamma, but had little effect on that induced by LPS. This suggests that sodium butyrate suppresses the IFN-gamma-induced iNOS expression by inhibiting the ERK to NF-kappa B pathway. In addition, it was found that sodium butyrate suppressed the IFN-gamma-induced interferon regulatory factor 1 (IRF-1) expression via the inhibition of ERK. Therefore, the ERK signaling pathway appears to play a key role in the sodium butyrate-mediated down-regulation of iNOS in the IFN-gamma-stimulated microglia. (C) 2005 Elsevier B.V All rights reserved.
引用
收藏
页码:56 / 64
页数:9
相关论文
共 31 条
[1]  
Bhat NR, 1998, J NEUROSCI, V18, P1633
[2]   AN IMMORTALIZED CELL-LINE EXPRESSES PROPERTIES OF ACTIVATED MICROGLIAL CELLS [J].
BOCCHINI, V ;
MAZZOLLA, R ;
BARLUZZI, R ;
BLASI, E ;
SICK, P ;
KETTENMANN, H .
JOURNAL OF NEUROSCIENCE RESEARCH, 1992, 31 (04) :616-621
[3]   MICROGLIAL-PRODUCED NITRIC-OXIDE AND REACTIVE NITROGEN-OXIDES MEDIATE NEURONAL CELL-DEATH [J].
BOJE, KM ;
ARORA, PK .
BRAIN RESEARCH, 1992, 587 (02) :250-256
[4]   Butyrate enema therapy stimulates mucosal repair in experimental colitis in the rat [J].
Butzner, JD ;
Parmar, R ;
Bell, CJ ;
Dalal, V .
GUT, 1996, 38 (04) :568-573
[5]   The inhibitory action of butyrate on lipopolysaccharide-induced nitric oxide production in RAW 264.7 murine macrophage cells [J].
Chakravortty, D ;
Koide, N ;
Kato, Y ;
Sugiyama, T ;
Mu, MM ;
Yoshida, T ;
Yokochi, T .
JOURNAL OF ENDOTOXIN RESEARCH, 2000, 6 (03) :243-247
[6]   Interleukin-1 and tumor necrosis factor-alpha synergistically mediate neurotoxicity: Involvement of nitric oxide and of N-methyl-D-aspartate receptors [J].
Chao, CC ;
Hu, SX ;
Ehrlich, L ;
Peterson, PK .
BRAIN BEHAVIOR AND IMMUNITY, 1995, 9 (04) :355-365
[7]   IFN-γ and IL-4 differently regulate inducible NO synthase gene expression through IRF-1 modulation [J].
Coccia, EM ;
Stellacci, E ;
Marziali, G ;
Weiss, G ;
Battistini, A .
INTERNATIONAL IMMUNOLOGY, 2000, 12 (07) :977-985
[8]   An interferon-gamma-activated site (GAS) is necessary for full expression of the mouse iNOS gene in response to interferon-gamma and lipopolysaccharide [J].
Gao, JJ ;
Morrison, DC ;
Parmely, TJ ;
Russell, SW ;
Murphy, WJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (02) :1226-1230
[9]   P2X7 nucleotide receptor activation enhances IFNγ-induced type II nitric oxide synthase activity in BV-2 microglial cells [J].
Gendron, FP ;
Chalimoniuk, M ;
Strosznajder, J ;
Shen, SM ;
González, FA ;
Weisman, GA ;
Sun, GY .
JOURNAL OF NEUROCHEMISTRY, 2003, 87 (02) :344-352
[10]   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