Defying death: the hepatocyte's survival kit

被引:22
作者
Schoemaker, MH
Moshage, H
机构
[1] Univ Groningen Hosp, Ctr Liver Digest & Metab Dis, NL-9700 RB Groningen, Netherlands
[2] Univ Groningen, Inst Drug Explorat, Dept Therapeut Gene Modulat, NL-9700 AC Groningen, Netherlands
关键词
apoptosis; cell death; hepatocyte; liver injury; survival; stellate cell; therapeutic intervention;
D O I
10.1042/CS20040090
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Acute liver injury can develop as a consequence of viral hepatitis, drug- or toxin-induced toxicity or rejection after liver transplantation, whereas chronic liver injury can be due to long-term exposure to alcohol, chemicals, chronic viral hepatitis, metabolic or cholestatic disorders. During liver injury, liver cells are exposed to increased levels of cytokines, bile acids and oxidative stress. This results in death of hepatocytes. In contrast, stellate cells become active and are resistant against cell death. Eventually, acute and chronic liver injury is followed by loss of liver function for which no effective therapies are available. Hepatocytes are well equipped with protective mechanisms to prevent cell death. As long as these protective mechanisms can be activated, the balance will be in favour of cell survival. However, the balance between cell survival and cell death is delicate and can be easily tipped towards cell death during liver injury. Therefore understanding the cellular mechanisms controlling death of liver cells is of clinical and scientific importance and can lead to the identification of novel intervention targets. This review describes some of the mechanisms that determine the balance between cell death and cell survival during liver diseases. The strict regulation of apoptotic cell death allows therapeutic intervention strategies. In this light, receptor-mediated apoptosis and mitochondria-mediated cell death are discussed and strategies are provided to selectively interfere with these processes.
引用
收藏
页码:13 / 25
页数:13
相关论文
共 146 条
[101]  
Shiraki K, 2003, INT J MOL MED, V12, P705
[102]  
SHOEMAKER MH, 2003, HEPATOLOGY, V38, pA143
[103]   Serial killers: ordering caspase activation events in apoptosis [J].
Slee, EA ;
Adrain, C ;
Martin, SJ .
CELL DEATH AND DIFFERENTIATION, 1999, 6 (11) :1067-1074
[104]   Vitamin E reduces oxidant injury to mitochondria and the hepatotoxicity of taurochenodeoxycholic acid in the rat [J].
Sokol, RJ ;
McKim, JM ;
Goff, MC ;
Ruyle, SZ ;
Devereaux, MW ;
Han, D ;
Packer, L ;
Everson, G .
GASTROENTEROLOGY, 1998, 114 (01) :164-174
[105]   Role of oxidant stress in the permeability transition induced in rat hepatic mitochondria by hydrophobic bile acids [J].
Sokol, RJ ;
Straka, MS ;
Dahl, R ;
Devereaux, MW ;
Yerushalmi, B ;
Gumpricht, E ;
Elkins, N ;
Everson, G .
PEDIATRIC RESEARCH, 2001, 49 (04) :519-531
[106]   RNA interference targeting Fas protects mice from fulminant hepatitis [J].
Song, EW ;
Lee, SK ;
Wang, J ;
Ince, N ;
Ouyang, N ;
Min, J ;
Chen, JS ;
Shankar, P ;
Lieberman, J .
NATURE MEDICINE, 2003, 9 (03) :347-351
[107]   Hepatic failure and liver cell damage in acute Wilson's disease involve CD95 (APO-1/Fas) mediated apoptosis [J].
Strand, S ;
Hofmann, WJ ;
Grambihler, A ;
Hug, H ;
Volkmann, M ;
Otto, G ;
Wesch, H ;
Mariani, SM ;
Hack, V ;
Stremmel, W ;
Krammer, PH ;
Galle, PR .
NATURE MEDICINE, 1998, 4 (05) :588-593
[108]   Tumor necrosis factor α in the pathogenesis of human and murine fulminant hepatic failure [J].
Streetz, K ;
Leifeld, L ;
Grundmann, D ;
Ramakers, J ;
Eckert, K ;
Spengler, U ;
Brenner, D ;
Manns, M ;
Trautwein, C .
GASTROENTEROLOGY, 2000, 119 (02) :446-460
[109]   Bcl-2 and Bcl-xL inhibit CD95-mediated apoptosis by preventing mitochondrial release of Smac/DIABLO and subsequent inactivation of X-linked inhibitor-of-apoptosis protein [J].
Sun, XM ;
Bratton, SB ;
Butterworth, M ;
MacFarlane, M ;
Cohen, GM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (13) :11345-11351
[110]   Molecular characterization of mitochondrial apoptosis-inducing factor [J].
Susin, SA ;
Lorenzo, HK ;
Zamzami, N ;
Marzo, I ;
Snow, BE ;
Brothers, GM ;
Mangion, J ;
Jacotot, E ;
Costantini, P ;
Loeffler, M ;
Larochette, N ;
Goodlett, DR ;
Aebersold, R ;
Siderovski, DP ;
Penninger, JM ;
Kroemer, G .
NATURE, 1999, 397 (6718) :441-446