TY - JOUR
T1 - Sleep-wake variation in body temperature regulates tau secretion and correlates with CSF and plasma tau
AU - Canet, Geoffrey
AU - Monteiro, Felipe Da Gama
AU - Rocaboy, Emma
AU - Diego-Diaz, Sofia
AU - Khelaifia, Boutheyna
AU - Godbout, Kelly
AU - Lachhab, Aymane
AU - Kim, Jessica
AU - Valencia, Daphne I.
AU - Yin, Audrey
AU - Wu, Hau Tieng
AU - Howell, Jordan
AU - Blank, Emily
AU - Laliberté, Francis
AU - Fortin, Nadia
AU - Boscher, Emmanuelle
AU - Fereydouni-Forouzandeh, Parissa
AU - Champagne, Stéphanie
AU - Guisle, Isabelle
AU - Hébert, Sébastien S.
AU - Pernet, Vincent
AU - Liu, Haiyan
AU - Lu, William
AU - Debure, Ludovic
AU - Rapoport, David M.
AU - Ayappa, Indu
AU - Varga, Andrew W.
AU - Parekh, Ankit
AU - Osorio, Ricardo S.
AU - Lacroix, Steve
AU - Burns, Mark P.
AU - Lucey, Brendan P.
AU - Blessing, Esther M.
AU - Planel, Emmanuel
N1 - Publisher Copyright:
© 2025, Canet et al.
PY - 2025/4/1
Y1 - 2025/4/1
N2 - Sleep disturbance is bidirectionally associated with an increased risk 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 the evidence that tau pathology spreads through neuron-to-neuron transfer, involving the secretion and internalization of pathological tau forms. Here, we combined 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, a higher BT during wakefulness and sleep deprivation increased CSF and plasma tau levels, while also upregulating unconventional protein secretion pathway I (UPS-I) events including (a) intracellular tau dephosphorylation, (b) caspase 3–mediated cleavage of tau (TauC3), and (c) membrane translocation of tau through binding to phosphatidylinositol 4,5-bisphosphate (PIP2) and syndecan 3. In humans, the increase in CSF and plasma tau levels observed after wakefulness correlated with BT increases 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.
AB - Sleep disturbance is bidirectionally associated with an increased risk 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 the evidence that tau pathology spreads through neuron-to-neuron transfer, involving the secretion and internalization of pathological tau forms. Here, we combined 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, a higher BT during wakefulness and sleep deprivation increased CSF and plasma tau levels, while also upregulating unconventional protein secretion pathway I (UPS-I) events including (a) intracellular tau dephosphorylation, (b) caspase 3–mediated cleavage of tau (TauC3), and (c) membrane translocation of tau through binding to phosphatidylinositol 4,5-bisphosphate (PIP2) and syndecan 3. In humans, the increase in CSF and plasma tau levels observed after wakefulness correlated with BT increases 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.
UR - https://www.scopus.com/pages/publications/105002568949
UR - https://www.scopus.com/pages/publications/105002568949#tab=citedBy
U2 - 10.1172/JCI182931
DO - 10.1172/JCI182931
M3 - Article
C2 - 39903530
AN - SCOPUS:105002568949
SN - 0021-9738
VL - 135
JO - Journal of Clinical Investigation
JF - Journal of Clinical Investigation
IS - 7
M1 - e182931
ER -