睡眠-觉醒时体温的变化可调节 tau 的分泌,并与脑脊液和血浆 tau 相关。

IF 13.3 1区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Geoffrey Canet, Felipe Da Gama Monteiro, Emma Rocaboy, Sofia Diego-Diaz, Boutheyna Khelaifia, Kelly Godbout, Aymane Lachhab, Jessica Kim, Daphne I Valencia, Audrey Yin, Hau-Tieng Wu, Jordan C Howell, Emily Blank, Francis Laliberté, Nadia Fortin, Emmanuelle Boscher, Parissa Fereydouni-Forouzandeh, Stéphanie Champagne, Isabelle Guisle, Sébastien S Hébert, Vincent Pernet, Haiyan Liu, William Lu, Ludovic Debure, David M Rapoport, Indu Ayappa, Andrew W Varga, Ankit Parekh, Ricardo S Osorio, Steve Lacroix, Mark P Burns, Brendan P Lucey, Esther M Blessing, Emmanuel Planel
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引用次数: 0

摘要

睡眠障碍与阿尔茨海默病和其他tau病风险的增加有双向关系。虽然睡眠-觉醒周期会调节间质和脑脊液(CSF)中的tau水平,但其潜在机制仍不清楚。有证据表明,tau病理学是通过神经元之间的转移传播的,涉及病理tau的分泌和内化,因此了解这些机制至关重要。在这里,我们结合体外、体内和临床方法,揭示了睡眠-觉醒周期中体温(BT)变化调节细胞外tau水平的途径。在小鼠中,清醒和睡眠剥夺期间较高的体温会增加脑脊液和血浆中的tau水平,同时也会上调非常规蛋白分泌途径-I(UPS-I)的成分,包括(i)细胞内tau去磷酸化,(ii)caspase-3介导的tau(TauC3)裂解,以及(iii)通过与PIP2和syndecan-3结合进行膜转运。在人体中,清醒后观察到的脑脊液和血浆tau水平的增加与清醒时BT的增加相关。我们的研究结果表明,睡眠-清醒时 BT 的变化会调节细胞外 tau 的水平,从而突出了体温调节在将睡眠障碍与 tau 介导的神经退行性变联系起来方面的重要性,以及热干预的预防潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sleep-wake variation in body temperature regulates tau secretion and correlates with CSF and plasma tau.

Sleep disturbance is bidirectionally associated with increased risks of Alzheimer's disease and other tauopathies. While the sleep-wake cycle regulates interstitial and cerebrospinal fluid (CSF) tau levels, the underlying mechanisms remain unknown. Understanding these mechanisms is crucial given evidence indicates that tau pathology spreads through neuron-to-neuron transfer, involving the secretion and internalization of pathological tau forms. Here, we combine in vitro, in vivo and clinical methods to reveal a pathway by which changes in body temperature (BT) over the sleep-wake cycle modulate extracellular tau levels. In mice, higher BT during wakefulness and sleep-deprivation increased CSF and plasma tau levels, while also upregulating unconventional protein secretion pathway-I (UPS-I) components, including (i) intracellular tau dephosphorylation, (ii) caspase-3-mediated cleavage of tau (TauC3) and (iii) its membrane translocation through binding to PIP2 and syndecan-3. In humans, the increase in CSF and plasma tau levels observed post-wakefulness correlated with BT increase during wakefulness. By demonstrating that sleep-wake variation in BT regulates extracellular tau levels, our findings highlight the importance of thermoregulation in linking sleep disturbances to tau-mediated neurodegeneration, and the preventative potential of thermal interventions.

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来源期刊
Journal of Clinical Investigation
Journal of Clinical Investigation 医学-医学:研究与实验
CiteScore
24.50
自引率
1.30%
发文量
1034
审稿时长
2 months
期刊介绍: The Journal of Clinical Investigation, established in 1924 by the ASCI, is a prestigious publication that focuses on breakthroughs in basic and clinical biomedical science, with the goal of advancing the field of medicine. With an impressive Impact Factor of 15.9 in 2022, it is recognized as one of the leading journals in the "Medicine, Research & Experimental" category of the Web of Science. The journal attracts a diverse readership from various medical disciplines and sectors. It publishes a wide range of research articles encompassing all biomedical specialties, including Autoimmunity, Gastroenterology, Immunology, Metabolism, Nephrology, Neuroscience, Oncology, Pulmonology, Vascular Biology, and many others. The Editorial Board consists of esteemed academic editors who possess extensive expertise in their respective fields. They are actively involved in research, ensuring the journal's high standards of publication and scientific rigor.
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