| 研究課題/領域番号 |
23K21394
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| 補助金の研究課題番号 |
21H02802 (2021-2023)
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| 研究種目 |
基盤研究(B)
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| 配分区分 | 基金 (2024)
補助金 (2021-2023) |
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| 応募区分 | 一般 |
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| 審査区分 |
小区分51020:認知脳科学関連
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| 研究機関 | 筑波大学 |
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研究代表者 |
ラザルス ミハエル 筑波大学, 国際統合睡眠医科学研究機構, 教授 (80469650)
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| 研究期間 (年度) |
2024-04-01 – 2026-03-31
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| 研究課題ステータス |
交付 (2024年度)
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| 配分額 *注記 |
17,030千円 (直接経費: 13,100千円、間接経費: 3,930千円)
2025年度: 1,560千円 (直接経費: 1,200千円、間接経費: 360千円)
2024年度: 3,770千円 (直接経費: 2,900千円、間接経費: 870千円)
2023年度: 3,770千円 (直接経費: 2,900千円、間接経費: 870千円)
2022年度: 3,770千円 (直接経費: 2,900千円、間接経費: 870千円)
2021年度: 4,160千円 (直接経費: 3,200千円、間接経費: 960千円)
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| キーワード | Sleep / Glia / sleep / glia / scRNAseq |
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| 研究開始時の研究の概要 |
The cellular and molecular processes underlying the build-up of sleepiness and maintenance of sleep are unknown. Glia are far from being merely support cells of the brain. The nucleus accumbens, a new sleep-regulating area through the integration of motivational stimuli provides an excellent opportunity to study the regulation of sleep and motivation by glia-neuron interactions.
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| 研究実績の概要 |
We have previously shown that the nucleus accumbens (NAc) is a novel brain region involved in sleep regulation, especially non-rapid eye movement sleep, by integrating motivational stimuli. We successfully demonstrated sleep induction in the NAc of freely behaving mice by increasing the activity of extracellular adenosine derived from astrocytes and neurons with a photoactivatable allosteric modulator of adenosine A2A receptors. We also showed that cytokine production in microglia during wakefulness is important for maintaining wakefulness, demonstrating the importance of glia-mediated neuroimmune interactions in the sleep-wake cycle.
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| 現在までの達成度 |
現在までの達成度
2: おおむね順調に進展している
理由
The paper, "Optochemical control of slow-wave sleep in the nucleus accumbens of male mice by a photoactivatable allosteric modulator of adenosine A2A receptors," has been published in the high-impact journal Nature Communications.
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| 今後の研究の推進方策 |
We continue to perform chemogenetic activation/inhibition of nucleus accumbens microglia and biochemical and genetic experiments to analyze the function of inflammation-related genes in the NAc. These analyses may help to unravel microglia-neuron interactions in sleep/wake regulation, provide new insights into the link between sleep homeostasis and immune resilience, and identify potential therapeutic targets for the treatment of sleep disorders.
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