Hepatic expression of multiple acute phase proteins and down-regulation of nuclear receptors after acute endotoxin exposure

被引:67
作者
Fang, C
Yoon, SJ
Tindberg, N
Järveläinen, HA
Lindros, KO
Ingelman-Sundberg, M [1 ]
机构
[1] Karolinska Inst, Inst Environm Med, Div Mol Toxicol, S-17177 Stockholm, Sweden
[2] Natl Publ Hlth Inst, Dept Alcohol Res, Helsinki, Finland
关键词
liver gene expressions; lipopolysaccharide; nuclear receptors; acute-phase reaction; hepatic injury; microarrays;
D O I
10.1016/j.bcp.2003.12.012
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Acute systemic lipopolysaccharide (endotoxin, LPS) exposure, which can lead to septic shock, enhances the hepatic expression of inflammatory and acute-phase proteins (APPs). To better understand how LPS aggravates damage, changes in hepatic gene expression after a single LPS dose was screened by using microarrays for 1176 rat genes. We detected more than 20 new potential LPS-induced APPs. Following acute LPS challenge, significant up-regulation of the steady-state mRNA levels of several important early transcription factors, such as c-jun and STAT3, and cytokine-associated genes, was observed. In contrast, RT-PCR analysis revealed marked down-regulation of the nuclear receptors RXRalpha, PXR, FXR, LXR, PPARalpha and CAR. Also genes encoding lipolytic, antioxidant as well as drug- and alcohol-metabolizing enzymes were down-regulated. These data suggest that acute LPS treatment induces important early transcription factors and co-ordinately down-regulates nuclear receptors, and that this results in altered expression of a large number of downstream genes. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:1389 / 1397
页数:9
相关论文
共 43 条
  • [31] Altered inotropic response to IGF-I in diabetic rat heart:: influence of intracellular Ca2+ and NO
    Ren, J
    Walsh, MF
    Hamaty, M
    Sowers, JR
    Brown, RA
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1998, 275 (03): : H823 - H830
  • [32] Sambrook J, 1989, MOL CLONING LAB MANU
  • [33] COOPERATIVE TRANSCRIPTIONAL ACTIVITY OF JUN AND STAT3-BETA, A SHORT-FORM OF STAT3
    SCHAEFER, TS
    SANDERS, LK
    NATHANS, D
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (20) : 9097 - 9101
  • [34] INDUCTION OF THE ACYL-COENZYME-A SYNTHETASE GENE BY FIBRATES AND FATTY-ACIDS IS MEDIATED BY A PEROXISOME PROLIFERATOR RESPONSE ELEMENT IN THE C-PROMOTER
    SCHOONJANS, K
    WATANABE, M
    SUZUKI, H
    MAHFOUDI, A
    KREY, G
    WAHLI, W
    GRIMALDI, P
    STAELS, B
    YAMAMOTO, T
    AUWERX, J
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (33) : 19269 - 19276
  • [35] Sterols and gene expression: control of affluence
    Schoonjans, K
    Brendel, C
    Mangelsdorf, D
    Auwerx, J
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2000, 1529 (1-3): : 114 - 125
  • [36] Schumann RR, 1996, MOL CELL BIOL, V16, P3490
  • [37] Sewer MB, 1996, DRUG METAB DISPOS, V24, P401
  • [38] POTENTIATION AND SUPPRESSION OF MOUSE-LIVER CYTOCHROME-P-450 ISOZYMES DURING THE ACUTE-PHASE RESPONSE INDUCED BY BACTERIAL-ENDOTOXIN
    STANLEY, LA
    ADAMS, DJ
    LINDSAY, R
    MEEHAN, RR
    LIAO, W
    WOLF, CR
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1988, 174 (01): : 31 - 36
  • [39] Diverse roles of the nuclear orphan receptor CAR in regulating hepatic genes in response to phenobarbital
    Ueda, A
    Hamadeh, HK
    Webb, HK
    Yamamoto, Y
    Sueyoshi, T
    Afshari, CA
    Lehmann, JM
    Negishi, M
    [J]. MOLECULAR PHARMACOLOGY, 2002, 61 (01) : 1 - 6
  • [40] Rapid up-regulation of I kappa B beta and abrogation of NF-kappa B activity in peritoneal macrophages stimulated with lipopolysaccharide
    Velasco, M
    DiazGuerra, MJM
    MartinSanz, P
    Alvarez, A
    Bosca, L
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (37) : 23025 - 23030