TNF-induced signaling in apoptosis

被引:376
作者
Rath, PC
Aggarwal, BB
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Mol Oncol, Cytokine Res Lab, Houston, TX 77030 USA
[2] Jawaharlal Nehru Univ, Sch Life Sci, New Delhi 110067, India
关键词
tumor necrosis factor; signaling; apoptosis;
D O I
10.1023/A:1020546615229
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Out of the almost 17 members of the TNF superfamily, TNF is probably the most potent inducer of apoptosis. TNF activates both cell-survival and cell-death mechanisms simultaneously. Activation of NF-kB-dependent genes regulates the survival and proliferative effects pf TNF, whereas activation of caspases regulates the apoptotic effects. TNF-induced apoptosis is mediated primarily through the activation of type I receptors, the death domain of which recruits more than a dozen different signaling proteins, which together are considered part of an apoptotic cascade. This cascade does not, however, account for the role of reactive oxygen intermediates, ceramide, phospholipases, and serine proteases which are also implicated in TNF-induced apoptosis. This cascade also does not explain how type II TNF receptors which lack the death domain, induce apoptosis. Nevertheless, this review of apoptosis signaling will be limited to those proteins that makeup the cascade.
引用
收藏
页码:350 / 364
页数:15
相关论文
共 210 条
[11]  
Bakker TR, 1999, INT J CANCER, V80, P320
[12]   The involvement of novel protein kinase C isozymes in influencing sensitivity of breast cancer MCF-7 cells to tumor necrosis factor-α [J].
Basu, A .
MOLECULAR PHARMACOLOGY, 1998, 53 (01) :105-111
[13]   An essential role for NF-kappa B in preventing TNF-alpha-induced cell death [J].
Beg, AA ;
Baltimore, D .
SCIENCE, 1996, 274 (5288) :782-784
[14]   Cell surface trafficking of Fas: A rapid mechanism of p53-mediated apoptosis [J].
Bennett, M ;
Macdonald, K ;
Chan, SW ;
Luzio, JP ;
Simari, R ;
Weissberg, P .
SCIENCE, 1998, 282 (5387) :290-293
[15]   Susceptibility to tumor necrosis factor alpha-induced apoptosis of mouse cells expressing polyomavirus middle and small T antigens [J].
Bergqvist, A ;
Soderbarg, K ;
Magnusson, G .
JOURNAL OF VIROLOGY, 1997, 71 (01) :276-283
[16]   CASEIN KINASE-1 PHOSPHORYLATES THE P75 TUMOR-NECROSIS-FACTOR RECEPTOR AND NEGATIVELY REGULATES TUMOR-NECROSIS-FACTOR SIGNALING FOR APOPTOSIS [J].
BEYAERT, R ;
VANHAESEBROECK, B ;
DECLERCQ, W ;
VANLINT, J ;
VANDENABEELE, P ;
AGOSTINIS, P ;
VANDENHEEDE, JR ;
FIERS, W .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (40) :23293-23299
[17]   Influence of cycloheximide-mediated downregulation of glucose transport on TNF alpha-induced apoptosis [J].
Binder, C ;
Binder, L ;
Kroemker, M ;
Schulz, M ;
Hiddemann, W .
EXPERIMENTAL CELL RESEARCH, 1997, 236 (01) :223-230
[18]   Involvement of MACH, a novel MORT1/FADD-interacting protease, in Fas/APO-1- and TNF receptor-induced cell death [J].
Boldin, MP ;
Goncharov, TM ;
Goltsev, YV ;
Wallach, D .
CELL, 1996, 85 (06) :803-815
[19]   Caspases induce cytochrome c release from mitochondria by activating cytosolic factors [J].
Bossy-Wetzel, E ;
Green, DR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (25) :17484-17490
[20]   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