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

期刊

CELL DEATH AND DIFFERENTIATION
卷 13, 期 5, 页码 852-860

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NATURE PUBLISHING GROUP
DOI: 10.1038/sj.cdd.4401837

关键词

Alzheimer; apoptosis; hippocampus; learning and memory; mitochondria

资金

  1. Intramural NIH HHS Funding Source: Medline

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Here we review evidence of roles for NF-kappa B in the regulation of developmental and synaptic plasticity, and cell survival in physiological and pathological settings. Signaling pathways modulating NF-kappa B activity include those engaged by neurotrophic factors, neurotransmitters, electrical activity, cytokines, and oxidative stress. Emerging findings support a pivotal role for NF-kappa B as a mediator of transcription-dependent enduring changes in the structure and function of neuronal circuits. Distinct subunits of NF-kappa B may uniquely affect cognition and behavior by regulating specific target genes. NF-kappa B 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-kappa B 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-kappa B in neurons are being elucidated and may provide novel targets for therapeutic intervention in various neurological disorders.

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