Molecular Neurobiology, Faculty of Biology, University of Bielefeld, Bielefeld, Germany.
PLoS One. 2012;7(2):e30838. doi: 10.1371/journal.pone.0030838. Epub 2012 Feb 1.
Cognitive decline during aging is correlated with a continuous loss of cells within the brain and especially within the hippocampus, which could be regenerated by adult neurogenesis. Here we show that genetic ablation of NF-κB resulted in severe defects in the neurogenic region (dentate gyrus) of the hippocampus. Despite increased stem cell proliferation, axogenesis, synaptogenesis and neuroprotection were hampered, leading to disruption of the mossy fiber pathway and to atrophy of the dentate gyrus during aging. Here, NF-κB controls the transcription of FOXO1 and PKA, regulating axogenesis. Structural defects culminated in behavioral impairments in pattern separation. Re-activation of NF-κB resulted in integration of newborn neurons, finally to regeneration of the dentate gyrus, accompanied by a complete recovery of structural and behavioral defects. These data identify NF-κB as a crucial regulator of dentate gyrus tissue homeostasis suggesting NF-κB to be a therapeutic target for treating cognitive and mood disorders.
衰老过程中的认知能力下降与大脑内细胞(尤其是海马内细胞)的持续丢失有关,而成年神经发生可以使这些细胞再生。在这里,我们发现 NF-κB 的基因缺失会导致海马神经发生区(齿状回)严重缺陷。尽管干细胞增殖增加,但轴突生成、突触生成和神经保护受到阻碍,导致苔藓纤维通路中断,并在衰老过程中导致齿状回萎缩。在这里,NF-κB 控制 FOXO1 和 PKA 的转录,调节轴突生成。结构缺陷最终导致模式分离的行为障碍。NF-κB 的重新激活导致新生神经元的整合,最终导致齿状回的再生,同时结构和行为缺陷完全恢复。这些数据表明 NF-κB 是齿状回组织内稳态的关键调节因子,提示 NF-κB 是治疗认知和情绪障碍的治疗靶点。