Dependence receptors: between life and death

被引:62
作者
Mehlen, P [1 ]
Thibert, C
机构
[1] Univ Lyon, CNRS,UMR 5534, Apoptosis Differentiat Lab, Equipe Labelisee La Ligue,Mol & Cellular Genet Ct, F-69622 Villeurbanne, France
[2] Buck Inst Agr Res, Novato, CA 94945 USA
关键词
dependence receptor; apoptosis; development; tumor suppressor; caspase;
D O I
10.1007/s00018-004-3467-7
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
The recently described family of dependence receptors is a new family of functionally related receptors. These proteins have little sequence similarity but display the common feature of inducing two completely opposite intracellular signals depending on ligand availability: in the presence of ligand, these receptors transduce a positive signal leading to survival, differentiation or migration, while in the absence of ligand, the receptors initiate or amplify a negative signal for apoptosis. Thus, cells that express these proteins manifest a state of dependence on their respective ligands. The mechanisms that trigger cell death induction in the absence of ligand are in large part unknown, but typically require cleavage by specific caspases. In this review we will present the proposed mechanisms for cell death induction by these receptors and their potential function in nervous system development and regulation of tumorigenesis.
引用
收藏
页码:1854 / 1866
页数:13
相关论文
共 108 条
[1]   TrnR2, a novel receptor that mediates neurturin and GDNF signaling through Ret [J].
Baloh, RH ;
Tansey, MG ;
Golden, JP ;
Creedon, DJ ;
Heuckeroth, RO ;
Keck, CL ;
Zimonjic, DB ;
Popescu, NC ;
Johnson, EM ;
Milbrandt, J .
NEURON, 1997, 18 (05) :793-802
[2]   THE P75 NERVE GROWTH-FACTOR RECEPTOR MEDIATES SURVIVAL OR DEATH DEPENDING ON THE STAGE OF SENSORY NEURON DEVELOPMENT [J].
BARRETT, GL ;
BARTLETT, PF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (14) :6501-6505
[3]  
Bloch-Gallego E, 1999, J NEUROSCI, V19, P4407
[4]   The RET proto-oncogene induces apoptosis: a novel mechanism for Hirschsprung disease [J].
Bordeaux, MC ;
Forcet, C ;
Granger, L ;
Corset, V ;
Bidaud, C ;
Billaud, M ;
Bredesen, DE ;
Edery, P ;
Mehlen, P .
EMBO JOURNAL, 2000, 19 (15) :4056-4063
[5]   p75NTR and the concept of cellular dependence:: seeing how the other half die [J].
Bredesen, DE ;
Ye, X ;
Tasinato, A ;
Sperandio, S ;
Wang, JJL ;
Assa-Munt, N ;
Rabizadeh, S .
CELL DEATH AND DIFFERENTIATION, 1998, 5 (05) :365-371
[6]   p75(NTR) and apoptosis: Trk-dependent and Trk-independent effects [J].
Bredesen, DE ;
Rabizadeh, S .
TRENDS IN NEUROSCIENCES, 1997, 20 (07) :287-290
[7]   GFRα1 is an essential receptor component for GDNF in the developing nervous system and kidney [J].
Cacalano, G ;
Fariñas, I ;
Wang, LC ;
Hagler, K ;
Forgie, A ;
Moore, M ;
Armanini, M ;
Phillips, H ;
Ryan, AM ;
Reichardt, LF ;
Hynes, M ;
Davies, A ;
Rosenthal, A .
NEURON, 1998, 21 (01) :53-62
[8]   Apoptotic pathway and MAPKs differentially regulate chemotropic responses of retinal growth cones [J].
Campbell, DS ;
Holt, CE .
NEURON, 2003, 37 (06) :939-952
[9]   Death of oligodendrocytes mediated by the interaction of nerve growth factor with its receptor p75 [J].
CasacciaBonnefil, P ;
Carter, BD ;
Dobrowsky, RT ;
Chao, MV .
NATURE, 1996, 383 (6602) :716-719
[10]   UNC-40, a C-elegans homolog of DCC (Deleted in Colorectal Cancer), is required in motile cells responding to UNC-6 netrin cues [J].
Chan, SSY ;
Zheng, H ;
Su, MW ;
Wilk, R ;
Killeen, MT ;
Hedgecock, EM ;
Culotti, JG .
CELL, 1996, 87 (02) :187-195