NF-κB in the survival and plasticity of neurons

被引:274
作者
Mattson, MP [1 ]
机构
[1] NIA, Neurosci Lab, Gerontol Res Ctr, Baltimore, MD 21224 USA
关键词
antioxidant; apoptosis; bcl-2; calcium; learning and memory; mitochondria; transcription;
D O I
10.1007/s11064-005-6961-x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The transcription factor nuclear factor kappa-B (NF-kappa B) is involved in regulating responses of neurons to activation of several different signaling pathways in a variety of physiological and pathological settings. During development of the nervous system NF-kappa B is activated in growing neurons by neurotrophic factors and can induce the expression of genes involved in cell differentiation and survival. In the mature nervous system NF-kappa B is activated in synapses in response to excitatory synaptic transmission and may play a pivotal role in processes such as learning and memory. NF-kappa B is activated in neurons and glial cells in acute neurodegenerative conditions such as stroke and traumatic injury, as well as in chronic neurodegenerative conditions such as Alzheimer's disease. Activation of NF-kappa B in neurons can promote their survival by inducing the expression of genes encoding anti-apoptotic proteins such as Bcl-2 and the antioxidant enzyme Mn-superoxide dismutase. On the other hand, by inducing the production and release of inflammatory cytokines, reactive oxygen molecules and excitotoxins, activation of NF-kappa B in microglia and astrocytes may contribute to neuronal degeneration. Emerging findings suggest roles for NF-kappa B as a mediator of effects of behavioral and dietary factors on neuronal plasticity. NF-kappa B provides an attractive target for the development of novel therapeutic approaches for a range of neurological disorders.
引用
收藏
页码:883 / 893
页数:11
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