Relationships between neuronal death and the cellular redox status. Focus on the developing nervous system

被引:120
作者
Castagne, V [1 ]
Gautschi, M [1 ]
Lefevre, K [1 ]
Posada, A [1 ]
Clarke, PGH [1 ]
机构
[1] Univ Lausanne, Inst Biol Cellulaire & Morphol, CH-1005 Lausanne, Switzerland
关键词
D O I
10.1016/S0301-0082(99)00012-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
During the development of the nervous system, a large number of neurons are eliminated through naturally occurring neuronal death. Many morphological and biochemical properties of such dying neurons are reminiscent of apoptosis, a type of death involving the action of genetically-programmed events but also epigenetic phenomena including oxidative stress. The following review contains three parts focusing respectively on basic knowledge of neuronal death and redox regulation, the mechanisms involved in neuronal death which are ordered in three sequential phases, and on the complex relations between neuronal fate and the redox status. Finally, we point out that oxidants are not always detrimental for neuronal survival. On the one hand, dying neurons often display signs of oxidative stress, including an elevation of their intracellular concentration of free radicals. Antioxidants may reduce the extent of neuronal death, suggesting a causal implication of free radicals in the death-process. On the other hand, at high concentrations antioxidants may lose their protective effects on developing neurons, and a non-lethal oxidative stress may potentiate the protective effects of other agents. These data suggest that free radicals; perhaps through their effects on cellular signalling pathways, may have positive effects on neuronal survival, provided that their intraneuronal concentrations are maintained at low levels. Much evidence suggests that the neuronal redox status must be maintained within a narrow range of values compatible with survival. Antioxidants may protect neurons subjected to an oxidative stress following axotomy or trophic factor-deprivation; but excessive reduction may become equally detrimental for neurons. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:397 / 423
页数:27
相关论文
共 448 条
[31]   Neurotrophin regulation of gene expression [J].
Bonni, A ;
Greenberg, ME .
CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES, 1997, 24 (04) :272-283
[32]   CEP-1347/KT7515, a JNK pathway inhibitor, supports the in vitro survival of chick embryonic neurons [J].
Borasio, GD ;
Horstmann, S ;
Anneser, JMH ;
Neff, NT ;
Glicksman, MA .
NEUROREPORT, 1998, 9 (07) :1435-1439
[33]   p75(NTR) and apoptosis: Trk-dependent and Trk-independent effects [J].
Bredesen, DE ;
Rabizadeh, S .
TRENDS IN NEUROSCIENCES, 1997, 20 (07) :287-290
[34]   Catalytic metals, ascorbate and free radicals: Combinations to avoid [J].
Buettner, GR ;
Jurkiewicz, BA .
RADIATION RESEARCH, 1996, 145 (05) :532-541
[35]   Programmed cell death in the developing nervous system [J].
Burek, MJ ;
Oppenheim, RW .
BRAIN PATHOLOGY, 1996, 6 (04) :427-446
[36]   Calcium permeability of glutamate-gated channels in the central nervous system [J].
Burnashev, N .
CURRENT OPINION IN NEUROBIOLOGY, 1996, 6 (03) :311-317
[37]   APOPTOSIS AND INCREASED GENERATION OF REACTIVE OXYGEN SPECIES IN DOWNS-SYNDROME NEURONS IN-VITRO [J].
BUSCIGLIO, J ;
YANKNER, BA .
NATURE, 1995, 378 (6559) :776-779
[38]   Mitochondrial control of apoptosis:: the role of cytochrome c [J].
Cai, JY ;
Yang, J ;
Jones, DP .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 1998, 1366 (1-2) :139-149
[39]   Communication -: Superoxide in apoptosis -: Mitochondrial generation triggered by cytochrome c loss [J].
Cai, JY ;
Jones, DP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (19) :11401-11404
[40]  
Cai ZZ, 1997, J BIOL CHEM, V272, P96