Redox regulation of cytokine expression in Kupffer cells

被引:70
作者
Tsukamoto, H
机构
[1] Univ So Calif, USC UCLA Res Ctr Alcohol Liver & Pancreat Dis, Los Angeles, CA 90033 USA
[2] Univ So Calif, Keck Sch Med, USC Res Ctr Liver Dis, Los Angeles, CA 90033 USA
[3] VA Greater Los Angeles Healthcare Syst, Los Angeles, CA 90033 USA
关键词
D O I
10.1089/152308602760598882
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
Kupffer cells, resident macrophages in the liver, play a central role in the homeostatic response to liver injury. Ironically, this defensive mechanism, if dysregulated, also works against the liver in acute and chronic liver damage. Central to this response is activation of nuclear factor-kappaB (NF-kappaB), a redox-sensitive transcription factor that transactivates promoters of many inflammatory genes, including cytokines. Much research has been devoted to identification of upstream signaling for activation of NF-kappaB, but the precise mechanism by which oxidant stress participates in this signaling is yet to be determined. Clues to this key question may be attained through studies on the mechanisms of sustained and/or accentuated NF-kappaB activation in hepatic macrophages in chronic liver diseases. This article reviews the literature on redox regulation of cytokine gene expression by Kupffer cells.
引用
收藏
页码:741 / 748
页数:8
相关论文
共 66 条
[1]   REDOX REGULATION OF FOS AND JUN DNA-BINDING ACTIVITY INVITRO [J].
ABATE, C ;
PATEL, L ;
RAUSCHER, FJ ;
CURRAN, T .
SCIENCE, 1990, 249 (4973) :1157-1161
[2]  
ADACHI Y, 1994, HEPATOLOGY, V20, P453, DOI 10.1002/hep.1840200227
[3]   SEPARATION OF OXIDANT-INITIATED AND REDOX-REGULATED STEPS IN THE NF-KAPPA-B SIGNAL-TRANSDUCTION PATHWAY [J].
ANDERSON, MT ;
STAAL, FJT ;
GITLER, C ;
HERZENBERG, LA ;
HERZENBERG, LA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (24) :11527-11531
[4]   Regulation of NF-κB RelA phosphorylation and transcriptional activity by p21ras and protein kinase Cζ in primary endothelial cells [J].
Anrather, J ;
Csizmadia, V ;
Soares, MP ;
Winkler, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (19) :13594-13603
[5]   SINUSOIDAL ENDOTHELIAL-CELL DAMAGE BY ACTIVATED MACROPHAGES IN RAT-LIVER NECROSIS [J].
ARAI, M ;
MOCHIDA, S ;
OHNO, A ;
OGATA, I ;
FUJIWARA, K .
GASTROENTEROLOGY, 1993, 104 (05) :1466-1471
[6]   NO+, NO(CENTER-DOT), AND NO- DONATION BY S-NITROSOTHIOLS - IMPLICATIONS FOR REGULATION OF PHYSIOLOGICAL FUNCTIONS BY S-NITROSYLATION AND ACCELERATION OF DISULFIDE FORMATION [J].
ARNELLE, DR ;
STAMLER, JS .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1995, 318 (02) :279-285
[7]   Modulation of lipopolysaccharide-mediated activation in rat Kupffer cells by antioxidants [J].
Bellezzo, JM ;
Leingang, KA ;
Bulla, GA ;
Britton, RS ;
Bacon, BR ;
Fox, ES .
JOURNAL OF LABORATORY AND CLINICAL MEDICINE, 1998, 131 (01) :36-44
[8]  
Bonizzi G, 1997, J IMMUNOL, V159, P5264
[9]   Interleukin-1 beta induces nuclear factor kappa B in epithelial cells independently of the production of reactive oxygen intermediates [J].
Bonizzi, G ;
Dejardin, E ;
Piret, B ;
Piette, J ;
Merville, MP ;
Bours, V .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1996, 242 (03) :544-549
[10]  
Bonizzi G, 1999, MOL CELL BIOL, V19, P1950