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核因子κB在神经细胞存活、可塑性及疾病中的作用。

Roles for NF-kappaB in nerve cell survival, plasticity, and disease.

作者信息

Mattson M P, Meffert M K

机构信息

Laboratory of Neurosciences, National Institute on Aging Intramural Research Program, Baltimore, MD 21224, USA.

出版信息

Cell Death Differ. 2006 May;13(5):852-60. doi: 10.1038/sj.cdd.4401837.

Abstract

Here we review evidence of roles for NF-kappaB in the regulation of developmental and synaptic plasticity, and cell survival in physiological and pathological settings. Signaling pathways modulating NF-kappaB activity include those engaged by neurotrophic factors, neurotransmitters, electrical activity, cytokines, and oxidative stress. Emerging findings support a pivotal role for NF-kappaB as a mediator of transcription-dependent enduring changes in the structure and function of neuronal circuits. Distinct subunits of NF-kappaB may uniquely affect cognition and behavior by regulating specific target genes. NF-kappaB activation can prevent the death of neurons by inducing the production of antiapoptotic proteins such as Bcl-2, IAPs and manganese superoxide dismutase (Mn-SOD). Recent findings indicate that NF-kappaB plays important roles in disorders such as epilepsy, stroke, Alzheimer's and Parkinson's diseases, as well as oncogenesis. Molecular pathways upstream and downstream of NF-kappaB in neurons are being elucidated and may provide novel targets for therapeutic intervention in various neurological disorders.

摘要

在此,我们综述了核因子κB(NF-κB)在发育和突触可塑性调节以及生理和病理环境下细胞存活中的作用证据。调节NF-κB活性的信号通路包括神经营养因子、神经递质、电活动、细胞因子和氧化应激所涉及的通路。新出现的研究结果支持NF-κB作为神经元回路结构和功能转录依赖性持久变化的介质发挥关键作用。NF-κB的不同亚基可能通过调节特定靶基因来独特地影响认知和行为。NF-κB激活可通过诱导抗凋亡蛋白如Bcl-2、凋亡抑制蛋白(IAPs)和锰超氧化物歧化酶(Mn-SOD)的产生来防止神经元死亡。最近的研究结果表明,NF-κB在癫痫、中风、阿尔茨海默病和帕金森病等疾病以及肿瘤发生中起重要作用。神经元中NF-κB上下游的分子通路正在被阐明,这可能为各种神经系统疾病的治疗干预提供新的靶点。

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