Lee Ivan T, Chang Alexander S, Manandhar Manabu, Shan Yongli, Fan Junmei, Izumo Mariko, Ikeda Yuichi, Motoike Toshiyuki, Dixon Shelley, Seinfeld Jeffrey E, Takahashi Joseph S, Yanagisawa Masashi
Department of Molecular Genetics, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390, USA; Department of Neuroscience, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390, USA.
Department of Molecular Genetics, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390, USA.
Neuron. 2015 Mar 4;85(5):1086-102. doi: 10.1016/j.neuron.2015.02.006.
Circadian behavior in mammals is orchestrated by neurons within the suprachiasmatic nucleus (SCN), yet the neuronal population necessary for the generation of timekeeping remains unknown. We show that a subset of SCN neurons expressing the neuropeptide neuromedin S (NMS) plays an essential role in the generation of daily rhythms in behavior. We demonstrate that lengthening period within Nms neurons is sufficient to lengthen period of the SCN and behavioral circadian rhythms. Conversely, mice without a functional molecular clock within Nms neurons lack synchronous molecular oscillations and coherent behavioral daily rhythms. Interestingly, we found that mice lacking Nms and its closely related paralog, Nmu, do not lose in vivo circadian rhythms. However, blocking vesicular transmission from Nms neurons with intact cell-autonomous clocks disrupts the timing mechanisms of the SCN, revealing that Nms neurons define a subpopulation of pacemakers that control SCN network synchrony and in vivo circadian rhythms through intercellular synaptic transmission.
哺乳动物的昼夜节律行为由视交叉上核(SCN)内的神经元协调,但维持计时功能所必需的神经元群体仍不清楚。我们发现,表达神经肽神经介素S(NMS)的SCN神经元亚群在行为的日常节律产生中起着至关重要的作用。我们证明,延长Nms神经元的周期足以延长SCN和行为昼夜节律的周期。相反,Nms神经元内缺乏功能性分子时钟的小鼠缺乏同步的分子振荡和连贯的行为昼夜节律。有趣的是,我们发现缺乏Nms及其密切相关的旁系同源物Nmu的小鼠并没有丧失体内昼夜节律。然而,用完整的细胞自主时钟阻断来自Nms神经元的囊泡传递会破坏SCN的计时机制,这表明Nms神经元定义了一个起搏器亚群,它们通过细胞间突触传递来控制SCN网络同步和体内昼夜节律。