Cell signaling in oxidative stress-induced liver injury

被引:138
作者
Czaja, Mark J.
机构
[1] Yeshiva Univ Albert Einstein Coll Med, Dept Med, Bronx, NY 10461 USA
[2] Yeshiva Univ Albert Einstein Coll Med, Marion Bessin Liver Res Ctr, Bronx, NY 10461 USA
关键词
liver injury; oxidative stress; extracellular signal-regulated kinase 1/2; c-Jun N-terminal kinase; nuclear factor kappa B;
D O I
10.1055/s-2007-991514
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Oxidative stress is a common mechanism of liver injury. Recent investigations have demonstrated that oxidant-induced liver injury is mediated by the direct effects of reactive oxygen species on signal transduction pathways. Although the function of cell signaling in this form of injury is complex and likely variable depending on the type and duration of oxidative stress, common regulatory pathways of hepatocyte oxidant injury have been identified that include the mitogen- activated protein kinases extracellular signal-regulated kinase 1/2 (ERK1/2) c-Jun N-terminal kinase (JNK), and the nuclear factor kappa B (NF-kappa B) pathway. Studies in cultured hepatocyte and rodent models of oxidative stress have demonstrated that ERK1/2 typically induces resistance to oxidant stress, whereas JNK promotes cell death. The effects of NF-kappa B activation are more complex and cell-type specific. A further understanding of the signaling pathways that regulate oxidant-induced liver injury may suggest new therapies for hepatic diseases resulting from oxidative stress.
引用
收藏
页码:378 / 389
页数:12
相关论文
共 100 条
[1]  
Albano E, 1996, HEPATOLOGY, V23, P155, DOI 10.1053/jhep.1996.v23.pm0008550035
[2]   The mitochondrial permeability transition is required for tumor necrosis factor alpha-mediated apoptosis and cytochrome c release [J].
Bradham, CA ;
Qian, T ;
Streetz, K ;
Trautwein, C ;
Brenner, DA ;
Lemasters, JJ .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (11) :6353-6364
[3]   The E3 ubiquitin ligase itch couples JNK activation to TNFα-induced cell death by inducing c-FLIPL turnover [J].
Chang, LF ;
Kamata, H ;
Solinas, G ;
Luo, JL ;
Maeda, S ;
Venuprasad, K ;
Liu, YC ;
Karin, M .
CELL, 2006, 124 (03) :601-613
[4]   Mammalian MAP kinase signalling cascades [J].
Chang, LF ;
Karin, M .
NATURE, 2001, 410 (6824) :37-40
[5]   Cytotoxicity and apoptosis produced by arachidonic acid in hep G2 cells overexpressing human cytochrome P4502E1 [J].
Chen, Q ;
Galleano, M ;
Cederbaum, AI .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (23) :14532-14541
[6]   Cytotoxicity and apoptosis produced by cytochrome P450 2E1 in Hep G2 cells [J].
Chen, Q ;
Cederbaum, AI .
MOLECULAR PHARMACOLOGY, 1998, 53 (04) :638-648
[7]   Selective glutathione depletion of mitochondria by ethanol sensitizes hepatocytes to tumor necrosis factor [J].
Colell, A ;
Gargía-Ruiz, C ;
Miranda, M ;
Ardite, E ;
Marí, M ;
Morales, A ;
Corrales, F ;
Kaplowitz, N ;
Fernández-Checa, JC .
GASTROENTEROLOGY, 1998, 115 (06) :1541-1551
[8]   C-jun NH2-terminal kinase (JNK)1 and JNK2 have distinct roles in CD8+ T cell activation [J].
Conze, D ;
Krahl, T ;
Kennedy, N ;
Weiss, L ;
Lumsden, J ;
Hess, P ;
Flavell, RA ;
Le Gros, G ;
Davis, RJ ;
Rincón, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 195 (07) :811-823
[9]   Oxidant-induced hepatocyte injury from menadione is regulated by ERK and AP-1 signaling [J].
Czaja, MJ ;
Liu, HL ;
Wang, YJ .
HEPATOLOGY, 2003, 37 (06) :1405-1413
[10]   The future of GI and liver research: Editorial perspectives - III. JNK/AP-1 regulation of hepatocyte death [J].
Czaja, MJ .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2003, 284 (06) :G875-G879