p75NTR and the concept of cellular dependence:: seeing how the other half die

被引:81
作者
Bredesen, DE [1 ]
Ye, X
Tasinato, A
Sperandio, S
Wang, JJL
Assa-Munt, N
Rabizadeh, S
机构
[1] Burnham Inst, Program Aging, La Jolla, CA 92037 USA
[2] Univ Calif San Diego, Dept Neurosci, La Jolla, CA 92093 USA
[3] Burnham Inst, Struct Biol Program, La Jolla, CA 92037 USA
[4] Univ Calif Los Angeles, Interdepartmental Program Neurosci, Los Angeles, CA 90024 USA
基金
美国国家科学基金会;
关键词
apoptosis; neurotrophin; receptor; cell death;
D O I
10.1038/sj.cdd.4400378
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
Cells depend on specific stimuli, such as trophic factors, for survival and in the absence of such stimuli, undergo apoptosis. How do cells initiate apoptosis in response to the withdrawal of trophic factors or other dependent stimuli? Recent studies of apoptosis induction by neurotrophin withdrawal argue for a novel form of pro-apoptotic signal transduction - 'negative signal transduction' - in which the absence of ligand-receptor interaction induces cell death. We have found that the prototype for this form of signaling - the common neurotrophin receptor, p75(NTR) - creates a state of cellular dependence (or addiction) on neurotrophins, and that this effect requires an 'addiction/dependence domain' (ADD) in the intracytoplasmic region of p75(NTR). We, have recently found other receptors that include dependence domains, arguing that dependence receptors, and their associated dependence domains, may be involved in a rather general mechanism to create cellular states of dependence on trophic factors, cytokines, adhesion, electrical activity and other dependent stimuli.
引用
收藏
页码:365 / 371
页数:7
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