神经科学
谷氨酸的
光遗传学
加巴能
非快速眼动睡眠
扁桃形结构
生物
丘脑
杏仁核
谷氨酸受体
眼球运动
抑制性突触后电位
生物化学
受体
作者
Chenyan Ma,Peng Zhong,Danqian Liu,Zeke Barger,Li Zhou,Wei-Cheng Chang,Brian Kim,Yang Dan
出处
期刊:Neuron
[Elsevier]
日期:2019-06-06
卷期号:103 (2): 323-334.e7
被引量:64
标识
DOI:10.1016/j.neuron.2019.05.015
摘要
A crucial step in understanding the sleep-control mechanism is to identify sleep neurons. Through systematic anatomical screening followed by functional testing, we identified two sleep-promoting neuronal populations along a thalamo-amygdala pathway, both expressing neurotensin (NTS). Rabies-mediated monosynaptic retrograde tracing identified the central nucleus of amygdala (CeA) as a major source of GABAergic inputs to multiple wake-promoting populations; gene profiling revealed NTS as a prominent marker for these CeA neurons. Optogenetic activation and inactivation of NTS-expressing CeA neurons promoted and suppressed non-REM (NREM) sleep, respectively, and optrode recording showed they are sleep active. Further tracing showed that CeA GABAergic NTS neurons are innervated by glutamatergic NTS neurons in a posterior thalamic region, which also promote NREM sleep. CRISPR/Cas9-mediated NTS knockdown in either the thalamic or CeA neurons greatly reduced their sleep-promoting effect. These results reveal a novel thalamo-amygdala circuit for sleep generation in which NTS signaling is essential for both the upstream glutamatergic and downstream GABAergic neurons.
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