Tumour necrosis factor-induced necrosis versus anti-Fas-induced apoptosis in L929 cells

被引:137
作者
Vercammen, D
Vandenabeele, P
Beyaert, R
Declercq, W
Fiers, W
机构
[1] FLANDERS INTERUNIV INST BIOTECHNOL,MOL BIOL LAB,B-9000 GHENT,BELGIUM
[2] STATE UNIV GHENT,B-9000 GHENT,BELGIUM
关键词
anti-Fas; apoptosis; CD95; necrosis; tumour necrosis factor;
D O I
10.1006/cyto.1997.0252
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
Murine fibrosarcoma L929 cells were transfected with human Pas cDNA. The mode of cell death was analysed following treatment either with tumour necrosis factor (TNF) or with agonistic antibodies to Pas. While triggering of the TNF receptors led to necrosis, clustering of the Pas antigen resulted in apoptotic cell death. N-tosyl-L-phenylalanine chloromethyl ketone and N alpha-p-tosyl-L-lysine chloromethyl ketone, two serine protease inhibitors, had a protective effect on TNF-induced killing, while Pas-mediated cell death was rather enhanced. Lithium chloride, which had a synergistic effect on TNF cytotoxicity, did not affect Pas-mediated death, whereas staurosporine had an enhancing effect on both types of cell death. Aphidicolin and hydroxyurea, inhibitors of DNA synthesis, were able to sensitize cells to Pas-induced killing, but had no effect on TNF cytotoxicity. Finally, we demonstrate that the effect of increasing concentrations of actinomycin D or cycloheximide is very different for the two types of cell killing. We conclude that either necrosis or apoptosis can occur in the same cell type, depending on the trigger, and that, although both pathways perhaps may share some cellular components, signal transduction is different for the two types of cell death. (C) 1997 Academic Press Limited.
引用
收藏
页码:801 / 808
页数:8
相关论文
共 29 条
[1]  
BERNANDESALNEMR.T, 1995, CANCER RES, V55, P6045
[2]  
BEYAERT R, 1993, CANCER RES, V53, P2623
[3]  
BEYAERT R, 1993, J IMMUNOL, V151, P291
[4]   LITHIUM-CHLORIDE POTENTIATES TUMOR NECROSIS FACTOR-MEDIATED CYTO-TOXICITY INVITRO AND INVIVO [J].
BEYAERT, R ;
VANHAESEBROECK, B ;
SUFFYS, P ;
VANROY, F ;
FIERS, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (23) :9494-9498
[5]   A NOVEL PROTEIN THAT INTERACTS WITH THE DEATH DOMAIN OF FAS/APO1 CONTAINS A SEQUENCE MOTIF RELATED TO THE DEATH DOMAIN [J].
BOLDIN, MP ;
VARFOLOMEEV, EE ;
PANCER, Z ;
METT, IL ;
CAMONIS, JH ;
WALLACH, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (14) :7795-7798
[6]   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
[7]   FADD, A NOVEL DEATH DOMAIN-CONTAINING PROTEIN, INTERACTS WITH THE DEATH DOMAIN OF FAS AND INITIATES APOPTOSIS [J].
CHINNAIYAN, AM ;
OROURKE, K ;
TEWARI, M ;
DIXIT, VM .
CELL, 1995, 81 (04) :505-512
[8]   A FAS-ASSOCIATED PROTEIN FACTOR, FAF1, POTENTIATES FAS-MEDIATED APOPTOSIS [J].
CHU, KT ;
NIU, XH ;
WILLIAMS, LT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (25) :11894-11898
[9]   MULTIPLE PATHWAYS ORIGINATE AT THE FAS/APO-1 (CD95) RECEPTOR - SEQUENTIAL INVOLVEMENT OF PHOSPHATIDYLCHOLINE-SPECIFIC PHOSPHOLIPASE-C AND ACIDIC SPHINGOMYELINASE IN THE PROPAGATION OF THE APOPTOTIC SIGNAL [J].
CIFONE, MG ;
RONCAIOLI, P ;
DEMARIA, R ;
CAMARDA, G ;
SANTONI, A ;
RUBERTI, G ;
TESTI, R .
EMBO JOURNAL, 1995, 14 (23) :5859-5868
[10]   RAIDD is a new 'death' adaptor molecule [J].
Duan, H ;
Dixit, VM .
NATURE, 1997, 385 (6611) :86-89