通过动态神经递质分离适应光周期

IF 50.5 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Nature Pub Date : 2024-07-17 DOI:10.1038/s41586-024-07692-7
G. Maddaloni, Y. J. Chang, R. A. Senft, S. M. Dymecki
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引用次数: 0

摘要

日照量(光周期)的变化会改变生理和行为1,2。对季节性光周期的适应性反应对所有生物都至关重要--光周期失调会导致疾病,包括情感障碍3 和代谢综合征4。昼夜节律回路与此类反应有关5,6,但人们对支持光周期变化相位同步的精确细胞基质知之甚少。在这里,我们发现了一种脑回路和轴突分支特异性可逆神经递质调配系统,它对行为和睡眠对光周期的适应至关重要。小鼠脑干正中饶舌核中一种名为 mrEn1-Pet17 的神经元将血清素从 VGLUT3(又称 SLC17A8,谷氨酸的代用品)分离到不同的轴突分支,这些分支支配着涉及昼夜节律和睡眠觉醒时间的特定脑区8,9。这种分支特异性神经递质调配并不区分白昼和黑夜阶段;但是,它会随着光周期的变化而重组。轴突(而非细胞体)在偏离赤经光照/黑暗条件时会改变神经化学表型,而在回到赤经条件时这些变化又会逆转。当我们从基因上禁用mrEn1-Pet1神经元中的Vglut3时,睡眠-觉醒期、自主活动和时钟基因表达并不与新的光周期同步或延迟。结合交叉狂犬病毒追踪和投射特异性神经元沉默,我们划定了视前区到 mrEn1Pet1 的连接,该连接负责解码光周期输入、驱动神经递质重组和促进行为同步。我们的研究结果揭示了调节生物体对光周期变化适应的大脑回路和周期性、分支特异性神经递质调配。
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Adaptation to photoperiod via dynamic neurotransmitter segregation
Changes in the amount of daylight (photoperiod) alter physiology and behaviour1,2. Adaptive responses to seasonal photoperiods are vital to all organisms—dysregulation associates with disease, including affective disorders3 and metabolic syndromes4. The circadian rhythm circuitry is implicated in such responses5,6, yet little is known about the precise cellular substrates that underlie phase synchronization to photoperiod change. Here we identify a brain circuit and system of axon branch-specific and reversible neurotransmitter deployment that are critical for behavioural and sleep adaptation to photoperiod. A type of neuron called mrEn1-Pet17 in the mouse brainstem median raphe nucleus segregates serotonin from VGLUT3 (also known as SLC17A8, a proxy for glutamate) to different axonal branches that innervate specific brain regions involved in circadian rhythm and sleep–wake timing8,9. This branch-specific neurotransmitter deployment did not distinguish between daylight and dark phase; however, it reorganized with change in photoperiod. Axonal boutons, but not cell soma, changed neurochemical phenotype upon a shift away from equinox light/dark conditions, and these changes were reversed upon return to equinox conditions. When we genetically disabled Vglut3 in mrEn1-Pet1 neurons, sleep–wake periods, voluntary activity and clock gene expression did not synchronize to the new photoperiod or were delayed. Combining intersectional rabies virus tracing and projection-specific neuronal silencing, we delineated a preoptic area-to-mrEn1Pet1 connection that was responsible for decoding the photoperiodic inputs, driving the neurotransmitter reorganization and promoting behavioural synchronization. Our results reveal a brain circuit and periodic, branch-specific neurotransmitter deployment that regulates organismal adaptation to photoperiod change. Changes in day length, conveyed by the preoptic area, drive axonal neurotransmitter reorganization in median raphe dual serotonin–glutamate neurons to regulate behaviour and sleep timing, highlighting a photoperiod-sensitive brain circuit.
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来源期刊
Nature
Nature 综合性期刊-综合性期刊
CiteScore
90.00
自引率
1.20%
发文量
3652
审稿时长
3 months
期刊介绍: Nature is a prestigious international journal that publishes peer-reviewed research in various scientific and technological fields. The selection of articles is based on criteria such as originality, importance, interdisciplinary relevance, timeliness, accessibility, elegance, and surprising conclusions. In addition to showcasing significant scientific advances, Nature delivers rapid, authoritative, insightful news, and interpretation of current and upcoming trends impacting science, scientists, and the broader public. The journal serves a dual purpose: firstly, to promptly share noteworthy scientific advances and foster discussions among scientists, and secondly, to ensure the swift dissemination of scientific results globally, emphasizing their significance for knowledge, culture, and daily life.
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