Lipopolysaccharide downregulates the expression of p53 through activation of MDM2 and enhances activation of nuclear factor-kappa B

被引:18
作者
Odkhuu, Erdenezaya [1 ,2 ]
Mendjargal, Adilsaikhan [3 ]
Koide, Naoki [1 ]
Naiki, Yoshikazu [1 ]
Komatsu, Takayuki [1 ]
Yokochi, Takashi [1 ]
机构
[1] Aichi Med Univ, Sch Med, Dept Microbiol & Immunol, Nagakute, Aichi 4801195, Japan
[2] Mongolian Natl Univ Med Sci, Dept Anat, Ulaanbaatar 210648, Mongolia
[3] Mongolian Natl Univ Med Sci, Ulaanbaatar 210648, Mongolia
关键词
Lipopolysaccharide; MDM2; NF-kappa B; Nutlin-3; P53; TUMOR-SUPPRESSOR P53; UBIQUITINATION; DEGRADATION; GENE; PHOSPHORYLATION; PROMOTES; PATHWAY;
D O I
10.1016/j.imbio.2014.08.010
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The effect of lipopolysaccharide (LPS) on the expression of p53 protein in RAW 264.7 macrophage cells was examined. LPS downregulated the expression of p53 protein 4-24 h after the stimulation. LPS-induced p53 inhibition was restored with pharmacological inhibitors of c-jun N-terminal kinase (JNK) and phosphatidylinositol 3-kinase (PI3K). It was also restored by inhibitors of MDM2 activation and proteasome. LPS-induced p53 inhibition corresponded to activation of MDM2. LPS-induced MDM2 activation was prevented by inhibitors of JNK and PI3K. The expression of p65 NF-kappa B at a late stage after LPS stimulation was downregulated in the presence of a MDM2 inhibitor. Nutlin-3 as a MDM2 inhibitor reduced LPS-induced production of nitric oxide but not tumor necrosis factor-alpha. Administration of LPS into mice downregulated the in vivo expression of p53 in the livers. Taken together, LPS was suggested to downregulate the expression of p53 via activation of MDM2 and enhance the activation of NF-kappa B at a late stage. (C) 2014 Elsevier GmbH. All rights reserved.
引用
收藏
页码:136 / 141
页数:6
相关论文
共 32 条
[1]   p53 and NF-κB: different strategies for responding to stress lead to a functional antagonism [J].
Ak, Prashanth ;
Levine, Arnold J. .
FASEB JOURNAL, 2010, 24 (10) :3643-3652
[2]  
[Anonymous], CURR PROTOC TOXICOL
[3]  
BURNETTE WN, 1981, ANAL BIOCHEM, V112, P195, DOI 10.1016/0003-2697(81)90281-5
[4]   Toll-like receptor-4 mediates lipopolysaccharide-induced signal transduction [J].
Chow, JC ;
Young, DW ;
Golenbock, DT ;
Christ, WJ ;
Gusovsky, F .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (16) :10689-10692
[5]   A critical role for p53 in the control of NF-κB-dependent gene expression in TLR4-stimulated dendritic cells exposed to genistein [J].
Dijsselbloem, Nathalie ;
Goriely, Stanislas ;
Albarani, Valentina ;
Gerlo, Sarah ;
Francoz, Sarah ;
Marine, Jean-Christophe ;
Goldman, Michel ;
Haegeman, Guy ;
Vanden Berghe, Wim .
JOURNAL OF IMMUNOLOGY, 2007, 178 (08) :5048-5057
[6]   Increased expression of p53 enhances transcription-coupled repair and global genomic repair of a UVC-damaged reporter gene in human cells [J].
Dregoesc, Diana ;
Rybak, Adrian P. ;
Rainbow, Andrew J. .
DNA REPAIR, 2007, 6 (05) :588-601
[7]   Mdm2 is a RING finger-dependent ubiquitin protein ligase for itself and p53 [J].
Fang, SY ;
Jensen, JP ;
Ludwig, RL ;
Vousden, KH ;
Weissman, AM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (12) :8945-8951
[8]   Stabilization of Mdm2 via decreased ubiquitination is mediated by protein kinase B/Akt-dependent phosphorylation [J].
Feng, JH ;
Tamaskovic, R ;
Yang, ZZ ;
Brazil, DP ;
Merlo, A ;
Hess, D ;
Hemmings, BA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (34) :35510-35517
[9]  
FRITSCHE M, 1993, ONCOGENE, V8, P307
[10]   JNK targets p53 ubiquitination and degradation in nonstressed cells [J].
Fuchs, SY ;
Adler, V ;
Buschmann, T ;
Yin, ZM ;
Wu, XW ;
Jones, SN ;
Ronai, Z .
GENES & DEVELOPMENT, 1998, 12 (17) :2658-2663