Division of Neurobiology, Department of Molecular and Cell Biology, Helen Wills Neuroscience Institute, Howard Hughes Medical Institute, University of California, Berkeley, Berkeley, CA 94720, USA.
Department of Bioengineering, University of California, San Diego, La Jolla, CA 92093, USA.
Cell. 2019 May 16;177(5):1293-1307.e16. doi: 10.1016/j.cell.2019.03.041. Epub 2019 Apr 25.
The perioculomotor (pIII) region of the midbrain was postulated as a sleep-regulating center in the 1890s but largely neglected in subsequent studies. Using activity-dependent labeling and gene expression profiling, we identified pIII neurons that promote non-rapid eye movement (NREM) sleep. Optrode recording showed that pIII glutamatergic neurons expressing calcitonin gene-related peptide alpha (CALCA) are NREM-sleep active; optogenetic and chemogenetic activation/inactivation showed that they strongly promote NREM sleep. Within the pIII region, CALCA neurons form reciprocal connections with another population of glutamatergic neurons that express the peptide cholecystokinin (CCK). Activation of CCK neurons also promoted NREM sleep. Both CALCA and CCK neurons project rostrally to the preoptic hypothalamus, whereas CALCA neurons also project caudally to the posterior ventromedial medulla. Activation of each projection increased NREM sleep. Together, these findings point to the pIII region as an excitatory sleep center where different subsets of glutamatergic neurons promote NREM sleep through both local reciprocal connections and long-range projections.
中脑的 perioculomotor(pIII)区域在 19 世纪 90 年代被认为是睡眠调节中枢,但在随后的研究中被很大程度上忽视了。使用活性依赖性标记和基因表达谱分析,我们确定了促进非快速眼动(NREM)睡眠的 pIII 神经元。光纤记录显示,表达降钙素基因相关肽 alpha(CALCA)的 pIII 谷氨酸能神经元在 NREM 睡眠中活跃;光遗传学和化学遗传学的激活/失活表明它们强烈促进 NREM 睡眠。在 pIII 区域内,CALCA 神经元与另一群表达肽胆囊收缩素(CCK)的谷氨酸能神经元形成相互连接。CCK 神经元的激活也促进了 NREM 睡眠。CALCA 和 CCK 神经元都向视前下丘脑投射,而 CALCA 神经元也向尾侧腹内侧髓质投射。每个投射的激活都增加了 NREM 睡眠。总的来说,这些发现表明 pIII 区域是一个兴奋性睡眠中枢,其中不同亚群的谷氨酸能神经元通过局部相互连接和长程投射来促进 NREM 睡眠。