cFLIP regulation of lymphocyte activation and development

被引:231
作者
Budd, RC [1 ]
Yeh, WC
Tschopp, J
机构
[1] Univ Vermont, Dept Med, Program Immunol, Burlington, VT 05405 USA
[2] Univ Toronto, Cambell Family Inst Brest Canc Res, Univ Hlth Network, Dept Med Biophys, Toronto, ON M5G 2C1, Canada
[3] Univ Lausanne, Dept Biochem, BIL Biomed Res Ctr, CH-1066 Epalinges, Switzerland
基金
美国国家卫生研究院; 加拿大健康研究院;
关键词
D O I
10.1038/nri1787
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cellular caspase-8 (FLICE)-like inhibitory protein (cFLIP) was originally identified as an inhibitor of death-receptor signalling through competition with caspase-8 for recruitment to FAS-associated via death domain ( FADD). More recently, it has been determined that both cFLIP and caspase-8 are required for the survival and proliferation of T cells following T-cell-receptor stimulation. This paradoxical finding launched new investigations of how these molecules might connect with signalling pathways that link to cell survival and growth following antigen-receptor activation. As discussed in this Review, insight gained from these studies indicates that cFLIP and caspase-8 form a heterodimer that ultimately links T-cell receptor signalling to activation of nuclear factor-kappa B through a complex that includes B-cell lymphoma 10 (BCL-10), mucosa-associated-lymphoid-tissue lymphoma-translocation gene 1 (MALT1) and receptor- interacting protein 1 (RIP1).
引用
收藏
页码:196 / 204
页数:9
相关论文
共 123 条
[81]   Transcription factors of the NFAT family: Regulation and function [J].
Rao, A ;
Luo, C ;
Hogan, PG .
ANNUAL REVIEW OF IMMUNOLOGY, 1997, 15 :707-747
[82]   Cell death attenuation by 'Usurpin', a mammalian DED-caspase homologue that precludes caspase-8 recruitment and activation by the CD-95 (Fas, APO-1) receptor complex [J].
Rasper, DM ;
Vaillancourt, JP ;
Hadano, S ;
Houtzager, VM ;
Seiden, I ;
Keen, SLC ;
Tawa, P ;
Xanthoudakis, S ;
Nasir, J ;
Martindale, D ;
Koop, BF ;
Peterson, EP ;
Thornberry, NA ;
Huang, JQ ;
MacPherson, DP ;
Black, SC ;
Hornung, F ;
Lenardo, MJ ;
Hayden, MR ;
Roy, S ;
Nicholson, DW .
CELL DEATH AND DIFFERENTIATION, 1998, 5 (04) :271-288
[83]   Biochemical mechanisms of IL-2-regulated Fas-mediated T cell apoptosis [J].
Refaeli, Y ;
Van Parijs, L ;
London, CA ;
Tschopp, J ;
Abbas, AK .
IMMUNITY, 1998, 8 (05) :615-623
[84]   Fas engagement induces the maturation of dendritic cells (DCs), the release of interleukin (IL)-1β, and the production of interferon γ in the absence of IL-12 during DC-T cell cognate interaction:: A new role for Fas ligand in inflammatory responses [J].
Rescigno, M ;
Piguet, V ;
Valzasina, B ;
Lens, S ;
Zubler, R ;
French, L ;
Kindler, V ;
Tschopp, J ;
Ricciardi-Castagnoli, P .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (11) :1661-1668
[85]   Direct repression of FLIP expression by c-myc is a major determinant of TRAIL sensitivity [J].
Ricci, MS ;
Jin, ZY ;
Dews, M ;
Yu, DN ;
Thomas-Tikhonenko, A ;
Dicker, DT ;
El-Deiry, WS .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (19) :8541-8555
[86]   The anti-apoptotic effect of Notch-1 requires p56lck-dependent, Akt/PKB-mediated signaling in T cells [J].
Sade, H ;
Krishna, S ;
Sarin, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (04) :2937-2944
[87]   Essential role for caspase 8 in T-cell homeostasis and T-cell-mediated immunity [J].
Salmena, L ;
Lemmers, B ;
Hakem, A ;
Matysiak-Zablocki, E ;
Murakami, K ;
Au, PYB ;
Berry, DM ;
Tamblyn, L ;
Shehabeldin, A ;
Migon, E ;
Wakeham, A ;
Bouchard, D ;
Yeh, WC ;
McGlade, JC ;
Ohashi, PS ;
Hakem, R .
GENES & DEVELOPMENT, 2003, 17 (07) :883-895
[88]   Phosphorylation of FADD/MORT1 at serine 194 and association with a 70-kDa cell cycle-regulated protein kinase [J].
Scaffidi, C ;
Volkland, J ;
Blomberg, I ;
Hoffmann, I ;
Krammer, PH ;
Peter, ME .
JOURNAL OF IMMUNOLOGY, 2000, 164 (03) :1236-1242
[89]  
Schlapbach R, 2000, EUR J IMMUNOL, V30, P3680, DOI 10.1002/1521-4141(200012)30:12<3680::AID-IMMU3680>3.0.CO
[90]  
2-L