An amygdalar oscillator coordinates cellular and behavioral rhythms.

IF 14.7 1区 医学 Q1 NEUROSCIENCES
Qiang Liu, Jiali Xiong, Dong Won Kim, Sang Soo Lee, Benjamin J Bell, Chloe Alexandre, Seth Blackshaw, Alban Latremoliere, Mark N Wu
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Abstract

Circadian rhythms are generated by the master pacemaker suprachiasmatic nucleus (SCN) in concert with local clocks throughout the body. Although many brain regions exhibit cycling clock gene expression, the identity of a discrete extra-SCN brain oscillator that produces rhythmic behavior has remained elusive. Here, we show that an extra-SCN oscillator in the lateral amygdala (LA) is defined by expression of the clock-output molecule mWAKE/ANKFN1. mWAKE is enriched in the anterior/dorsal LA (adLA), and, strikingly, selective disruption of clock function or excitatory signaling in adLAmWAKE neurons abolishes Period2 (PER2) rhythms throughout the LA. mWAKE levels rise at night and promote rhythmic excitability of adLAmWAKE neurons by upregulating Ca2+-activated K+ channel activity specifically at night. adLAmWAKE neurons coordinate rhythmic sensory perception and anxiety in a clock-dependent and WAKE-dependent manner. Together, these data reveal the cellular identity of an extra-SCN brain oscillator and suggest a multi-level hierarchical system organizing molecular and behavioral rhythms.

杏仁核振荡器能协调细胞和行为节奏。
昼夜节律是由起搏器上核(SCN)与全身的局部时钟协同产生的。虽然许多脑区都表现出周期性的时钟基因表达,但产生节律行为的离散的SCN外脑振荡器的身份却一直难以确定。在这里,我们发现外侧杏仁核(LA)中的SCN外振荡器是由时钟输出分子mWAKE/ANKFN1的表达所决定的。mWAKE富集在LA的前部/背侧(adLA),而且令人震惊的是,选择性地破坏adLAmWAKE神经元的时钟功能或兴奋信号传导会取消整个LA的Period2(PER2)节律。mWAKE水平在夜间升高,并通过上调Ca2+激活的K+通道活性促进adLAmWAKE神经元的节律性兴奋,特别是在夜间。adLAmWAKE神经元以时钟依赖和WAKE依赖的方式协调节律性感觉知觉和焦虑。这些数据共同揭示了SCN外大脑振荡器的细胞特性,并提出了一个组织分子和行为节律的多层次分级系统。
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来源期刊
Neuron
Neuron 医学-神经科学
CiteScore
24.50
自引率
3.10%
发文量
382
审稿时长
1 months
期刊介绍: Established as a highly influential journal in neuroscience, Neuron is widely relied upon in the field. The editors adopt interdisciplinary strategies, integrating biophysical, cellular, developmental, and molecular approaches alongside a systems approach to sensory, motor, and higher-order cognitive functions. Serving as a premier intellectual forum, Neuron holds a prominent position in the entire neuroscience community.
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