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Molecular and Cellular Biology, August 2001, p. 5299-5305, Vol. 21, No. 16
Institute of Biochemistry, University of
Lausanne, BIL Biomedical Research Center,1
and Apotech Biochemicals,
Biopôle,2 CH-1066 Epalinges, Switzerland
Received 1 February 2001/Returned for modification 16 March
2001/Accepted 24 May 2001
Activation of the transcription factor NF-
0270-7306/01/$04.00+0 DOI: 10.1128/MCB.21.16.5299-5305.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
NF-
B Signals Induce the Expression of
c-FLIP
B is a major effector
of the inducible resistance to death receptor-mediated apoptosis. Previous evidence indicates that the combined transcriptional activation of TRAF-1, TRAF-2, IAP-1, and IAP-2 is required to suppress
cell death by tumor necrosis factor (TNF). Here we show that NF-
B
activation upregulates the caspase 8 inhibitor FLIP, resulting in
increased resistance to Fas ligand (FasL) or TNF. Restoration of either
the full-length 55-kDa long form of FLIP or an alternatively spliced
short form of FLIP in NF-
B null cells inhibits TNF- and FasL-induced
cell death efficiently, whereas the expression of IAP or TRAF family
members only partially rescues cells from death. Resistance to either
FasL- or TNF-induced apoptosis is overcome when cells are incubated in
the presence of the protein synthesis inhibitor cycloheximide. This
treatment leads to the rapid downregulation of FLIP but not to that of
TRAF2. Our findings suggest that FLIP is an important mediator of
NF-
B-controlled antiapoptotic signals.
*
Corresponding author. Mailing address: Institute of
Biochemistry, University of Lausanne, Ch. des Boveresses 155, CH-1066 Epalinges, Switzerland. Phone: 41 21 692 5738. Fax: 41 21 692 5705. E-mail: jurg.tschopp{at}ib.unil.ch.
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