Astrocyte calcium dysfunction causes early network hyperactivity in Alzheimer's Disease
Disha ShahiD, Willy GselliD, Jérôme WahisiD, Emma Susanne LuckettiD, Tarik Jamoulle, Ben VermaerckeiD, Pranav PremaniD, Daan MoecharsiD, Véronique HendrickxiD, Tom JaspersiD, Katleen CraessaertsiD, Katrien HorréiD, Leen WolfsiD, Mark W. E. J. FiersiD, Matthew G. HoltiD, Dietmar Rudolf ThaliD, Zsuzsanna Callaerts‐VeghiD, Rudi D’HoogeiD, Rik R. VandenbergheiD, Uwe HimmelreichiD, Vincent BoniniD, Bart De StrooperiD
Abstract
Dysfunctions of network activity and functional connectivity (FC) represent early events in Alzheimers disease (AD), but the underlying mechanisms remain unclear. Astrocytes regulate neuronal activity in the healthy brain, but their involvement in early network hyperactivity in AD is unknown. We show increased FC in the human cingulate cortex, several years before amyloid deposition. We found the same early cingulate FC disruption and neuronal hyperactivity in AppNL-F mice. Crucially, these network disruptions are accompanied by decreased astrocyte calcium signaling. Recovery of astroglial calcium activity normalizes neuronal hyperactivity and FC, as well as seizure susceptibility and day/night behavioral hyperactivity. In conclusion, we show for the first time that astrocytes mediate initial features of AD and drive clinically relevant phenotypes.
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