Connexin 43-Mediated Astroglial Metabolic Networks Contribute to the Regulation of the Sleep-Wake Cycle

被引:141
|
作者
Clasadonte, Jerome [1 ,2 ,3 ]
Scemes, Eliana [4 ]
Wang, Zhongya [5 ]
Boison, Detlev [5 ]
Haydon, Philip G. [1 ]
机构
[1] Tufts Univ, Sch Med, Dept Neurosci, Boston, MA 02111 USA
[2] Jean Pierre Aubert Res Ctr, Lab Dev & Plast Neuroendocrine Brain, INSERM, F-U1172 Lille, France
[3] Univ Lille, Sch Med, FHU Days Hlth 1000, Lille, France
[4] Albert Einstein Coll Med, Dominick P Purpura Dept Neurosci, Bronx, NY 10467 USA
[5] Legacy Res Inst, Robert Stone Dow Neurobiol Labs, Portland, OR USA
基金
欧盟地平线“2020”;
关键词
ASTROCYTE-SPECIFIC EXPRESSION; GAP JUNCTIONAL COMMUNICATION; BRAIN ENERGY-METABOLISM; OREXIN/HYPOCRETIN NEURONS; HYPOCRETIN-OREXIN; GENE DELIVERY; NARCOLEPSY; LACTATE; MICE; RELEASE;
D O I
10.1016/j.neuron.2017.08.022
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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.
引用
收藏
页码:1365 / +
页数:21
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