Mechanisms of liver cell injury

被引:231
作者
Kaplowitz, N
机构
[1] Univ So Calif, Res Ctr Liver Dis, Los Angeles, CA USA
[2] Univ So Calif, Keck Sch Med, Div Gastrointestinal & Liver Dis, Los Angeles, CA USA
关键词
apoptosis; caspases; necrosis; oxidative stress;
D O I
10.1016/S0168-8278(00)80414-6
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Liver cell death is triggered by a number of insults arising from the external environment or from within the cell. These insults may engage cell surface receptors with death domaines leading to a proteolytic cascade involving initiator and executioner caspases and an apoptotic demise. Alternatively, the insults may profoundly disrupt mitochondrial function and result in loss of homeostasis accompanied by activation of hydrolases and a necrotic or lyric demise. The distinction between apoptotic and necrotic cell death has become blurred recently by the recognition that the same stimuli can induce either form of cell, death as well as caspase independent apoptosis, Mitochondria play a key role in the shape of cell death; selective release of mediators amplifies the apoptosis program and profound loss of mitochondrial function leads to necrosis, Reactive oxygen metabolites and nitric oxide participate as intitiating factors and modulators. The extensive knowledge gained in recent years about the mechanisms of cell death will undoubtedly lead to new and exciting advances in the prevention and treatment of liver diseases. Important targets include death receptors, death signaling mechanisms, the mitochondrial permeability transition and approaches which selectively inhibit or activate cell death in parenchymal versus nonparenchymal cells.
引用
收藏
页码:39 / 47
页数:9
相关论文
共 66 条
[1]   The Bcl-2 protein family: Arbiters of cell survival [J].
Adams, JM ;
Cory, S .
SCIENCE, 1998, 281 (5381) :1322-1326
[2]   Death receptors: Signaling and modulation [J].
Ashkenazi, A ;
Dixit, VM .
SCIENCE, 1998, 281 (5381) :1305-1308
[3]   CHRONIC ETHANOL FEEDING INCREASES APOPTOSIS AND CELL-PROLIFERATION IN RAT-LIVER [J].
BARONI, GS ;
MARUCCI, L ;
BENEDETTI, A ;
MANCINI, R ;
JEZEQUEL, AM ;
ORLANDI, F .
JOURNAL OF HEPATOLOGY, 1994, 20 (04) :508-513
[4]   SUBCELLULAR CHANGES AND APOPTOSIS INDUCED BY ETHANOL IN RAT-LIVER [J].
BENEDETTI, A ;
BRUNELLI, E ;
RISICATO, R ;
CILLUFFO, T ;
JEZEQUEL, AM ;
ORLANDI, F .
JOURNAL OF HEPATOLOGY, 1988, 6 (02) :137-143
[5]   Apoptosis without caspases: an inefficient molecular guillotine? [J].
Borner, C ;
Monney, L .
CELL DEATH AND DIFFERENTIATION, 1999, 6 (06) :497-507
[6]  
BOTLA R, 1995, J PHARMACOL EXP THER, V272, P930
[7]  
Bradham CA, 1998, AM J PHYSIOL-GASTR L, V275, pG387, DOI 10.1152/ajpgi.1998.275.3.G387
[8]   Communication -: Superoxide in apoptosis -: Mitochondrial generation triggered by cytochrome c loss [J].
Cai, JY ;
Jones, DP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (19) :11401-11404
[9]   Suppression of tumor necrosis factor-induced cell death by inhibitor of apoptosis c-IAP2 is under NF-kappa B control [J].
Chu, ZL ;
McKinsey, TA ;
Liu, L ;
Gentry, JJ ;
Malim, MH ;
Ballard, DW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (19) :10057-10062
[10]   Transport of reduced glutathione in hepatic mitochondria and mitoplasts from ethanol-treated rats: Effect of membrane physical properties and S-adenosyl-L-methionine [J].
Colell, A ;
GarciaRuiz, C ;
Morales, A ;
Ballesta, A ;
Ookhtens, M ;
Rodes, J ;
Kaplowitz, N ;
FernandezCheca, JC .
HEPATOLOGY, 1997, 26 (03) :699-708