Dynamics of glia and neurons regulate homeostatic rest, sleep and feeding behavior in Drosophila

IF 21.2 1区 医学 Q1 NEUROSCIENCES
Andres Flores-Valle, Ivan Vishniakou, Johannes D. Seelig
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Abstract

Homeostatic processes, including sleep, are critical for brain function. Here we identify astrocyte-like glia (or astrocytes, AL) and ensheathing glia (EG), the two major classes of glia that arborize inside the brain, as brain-wide, locally acting homeostats for the short, naturally occurring rest and sleep bouts of Drosophila, and show that a subset of neurons in the fan-shaped body encodes feeding homeostasis. We show that the metabolic gas carbon dioxide, changes in pH and behavioral activity all induce long-lasting calcium responses in EG and AL, and that calcium levels in both glia types show circadian modulation. The homeostatic dynamics of these glia can be modeled based on behavior. Additionally, local optogenetic activation of AL or EG is sufficient to induce rest. Together, these results suggest that glial calcium levels are homeostatic controllers of metabolic activity, thus establishing a link between metabolism, rest and sleep.

Abstract Image

神经胶质和神经元的动态调节果蝇的内稳态休息、睡眠和摄食行为
包括睡眠在内的内稳态过程对大脑功能至关重要。在这里,我们确定了星形细胞样胶质细胞(或星形胶质细胞,AL)和鞘鞘胶质细胞(EG),这两种主要的胶质细胞分布在大脑内部,作为果蝇短暂的、自然发生的休息和睡眠期间的全脑局部作用的稳态调节器,并表明扇形身体中的一个神经元子集编码喂养稳态。我们发现,代谢气体二氧化碳、pH值变化和行为活动都能诱导EG和AL的长期钙反应,并且两种胶质细胞的钙水平都表现出昼夜节律调节。这些胶质细胞的内稳态动力学可以基于行为建模。此外,AL或EG的局部光遗传激活足以诱导休息。综上所述,这些结果表明,神经胶质钙水平是代谢活动的稳态控制者,因此在代谢、休息和睡眠之间建立了联系。
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来源期刊
Nature neuroscience
Nature neuroscience 医学-神经科学
CiteScore
38.60
自引率
1.20%
发文量
212
审稿时长
1 months
期刊介绍: Nature Neuroscience, a multidisciplinary journal, publishes papers of the utmost quality and significance across all realms of neuroscience. The editors welcome contributions spanning molecular, cellular, systems, and cognitive neuroscience, along with psychophysics, computational modeling, and nervous system disorders. While no area is off-limits, studies offering fundamental insights into nervous system function receive priority. The journal offers high visibility to both readers and authors, fostering interdisciplinary communication and accessibility to a broad audience. It maintains high standards of copy editing and production, rigorous peer review, rapid publication, and operates independently from academic societies and other vested interests. In addition to primary research, Nature Neuroscience features news and views, reviews, editorials, commentaries, perspectives, book reviews, and correspondence, aiming to serve as the voice of the global neuroscience community.
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