Physiological synaptic activity and recognition memory are fueled by astroglial glutamine
Giselle T. Y. CheungiD, Danijela BataveljićiD, Naresh KumariD, Julien MoulardiD, Glenn M. DalléraciD, Josien VisseriD, Astrid RollenhageniD, Cédric MonginiD, Oana CheveriD, Alexis‐Pierre BemelmansiD, Joachim H. R. LübkeiD, Isabelle LerayiD, Nathalie RouachiD
Abstract
Presynaptic glutamate replenishment is fundamental to brain function. In high activity regimes, such as epileptic episodes, this process is thought to rely on the glutamate-glutamine cycle between neurons and astrocytes. However the presence of an astroglial glutamine supply, as well as its functional relevance in vivo in the healthy brain remain controversial, partly due to a lack of tools that can directly examine glutamine transfer. Here, we generated a novel fluorescent probe that tracks glutamine in live cells, which provided direct visual evidence of an activity-dependent glutamine supply from astroglial networks to presynaptic structures under physiological conditions. This mobilization is mediated by connexin43, an astroglial protein with both gap-junction and hemichannel functions, and is essential for synaptic transmission and object recognition memory. Our findings uncover an indispensable recruitment of astroglial glutamine in physiological synaptic activity and memory via an unconventional pathway, thus providing an astrocyte basis for cognitive processes.
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