Clasadonte Jerome, Scemes Eliana, Wang Zhongya, Boison Detlev, Haydon Philip G
Department of Neuroscience, Tufts University School of Medicine, Boston, MA, USA; Inserm, Laboratory of Development and Plasticity of the Neuroendocrine Brain, Jean-Pierre Aubert Research Center, U1172, Lille, France; University of Lille, FHU 1000 days for Health, School of Medicine, Lille, France.
Dominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, NY, USA.
Neuron. 2017 Sep 13;95(6):1365-1380.e5. doi: 10.1016/j.neuron.2017.08.022. Epub 2017 Aug 31.
Astrocytes produce and supply metabolic substrates to neurons through gap junction-mediated astroglial networks. However, the role of astroglial metabolic networks in behavior is unclear. Here, we demonstrate that perturbation of astroglial networks impairs the sleep-wake cycle. Using a conditional Cre-Lox system in mice, we show that knockout of the gap junction subunit connexin 43 in astrocytes throughout the brain causes excessive sleepiness and fragmented wakefulness during the nocturnal active phase. This astrocyte-specific genetic manipulation silenced the wake-promoting orexin neurons located in the lateral hypothalamic area (LHA) by impairing glucose and lactate trafficking through astrocytic networks. This global wakefulness instability was mimicked with viral delivery of Cre recombinase to astrocytes in the LHA and rescued by in vivo injections of lactate. Our findings propose a novel regulatory mechanism critical for maintaining normal daily cycle of wakefulness and involving astrocyte-neuron metabolic interactions.
星形胶质细胞通过缝隙连接介导的星形胶质网络产生并向神经元提供代谢底物。然而,星形胶质代谢网络在行为中的作用尚不清楚。在此,我们证明星形胶质网络的扰动会损害睡眠-觉醒周期。利用小鼠中的条件性Cre-Lox系统,我们发现全脑星形胶质细胞中缝隙连接亚基连接蛋白43的敲除会导致夜间活跃期过度嗜睡和觉醒碎片化。这种星形胶质细胞特异性的基因操作通过损害葡萄糖和乳酸通过星形胶质网络的运输,使位于下丘脑外侧区(LHA)的促觉醒食欲素神经元沉默。通过将Cre重组酶病毒递送至LHA的星形胶质细胞可模拟这种整体觉醒不稳定性,并通过体内注射乳酸来挽救。我们的研究结果提出了一种新的调节机制,该机制对于维持正常的每日觉醒周期至关重要,并且涉及星形胶质细胞-神经元代谢相互作用。