Kobayashi Yohei, Ye Zhanlei, Hensch Takao K
Center for Brain Science, Department of Molecular Cellular Biology, Harvard University, 52 Oxford Street, Cambridge, MA 02138, USA; F.M. Kirby Neurobiology Center, Department of Neurology, Boston Children's Hospital, Harvard Medical School, 300 Longwood Avenue, Boston, MA 02115, USA.
Center for Brain Science, Department of Molecular Cellular Biology, Harvard University, 52 Oxford Street, Cambridge, MA 02138, USA.
Neuron. 2015 Apr 8;86(1):264-75. doi: 10.1016/j.neuron.2015.02.036. Epub 2015 Mar 19.
Circadian rhythms control a variety of physiological processes, but whether they may also time brain development remains largely unknown. Here, we show that circadian clock genes control the onset of critical period plasticity in the neocortex. Within visual cortex of Clock-deficient mice, the emergence of circadian gene expression was dampened, and the maturation of inhibitory parvalbumin (PV) cell networks slowed. Loss of visual acuity in response to brief monocular deprivation was concomitantly delayed and rescued by direct enhancement of GABAergic transmission. Conditional deletion of Clock or Bmal1 only within PV cells recapitulated the results of total Clock-deficient mice. Unique downstream gene sets controlling synaptic events and cellular homeostasis for proper maturation and maintenance were found to be mis-regulated by Clock deletion specifically within PV cells. These data demonstrate a developmental role for circadian clock genes outside the suprachiasmatic nucleus, which may contribute mis-timed brain plasticity in associated mental disorders.
昼夜节律控制着多种生理过程,但它们是否也能调节大脑发育在很大程度上仍不清楚。在这里,我们表明昼夜节律时钟基因控制着新皮质关键期可塑性的开始。在Clock基因缺陷小鼠的视觉皮质内,昼夜节律基因表达的出现受到抑制,抑制性小白蛋白(PV)细胞网络的成熟减缓。对短暂单眼剥夺的视力丧失反应也随之延迟,并通过直接增强GABA能传递得以挽救。仅在PV细胞内条件性删除Clock或Bmal1可重现完全Clock基因缺陷小鼠的结果。发现控制突触事件和细胞内稳态以实现正常成熟和维持的独特下游基因集在PV细胞内被Clock基因删除特异性地错误调节。这些数据证明了视交叉上核以外的昼夜节律时钟基因在发育中的作用,这可能导致相关精神障碍中大脑可塑性的时间失调。