| Literature DB >> 29804835 |
Adar Adamsky1, Adi Kol1, Tirzah Kreisel1, Adi Doron1, Nofar Ozeri-Engelhard1, Talia Melcer1, Ron Refaeli1, Henrike Horn1, Limor Regev1, Maya Groysman2, Michael London3, Inbal Goshen4.
Abstract
Astrocytes respond to neuronal activity and were shown to be necessary for plasticity and memory. To test whether astrocytic activity is also sufficient to generate synaptic potentiation and enhance memory, we expressed the Gq-coupled receptor hM3Dq in CA1 astrocytes, allowing their activation by a designer drug. We discovered that astrocytic activation is not only necessary for synaptic plasticity, but also sufficient to induce NMDA-dependent de novo long-term potentiation in the hippocampus that persisted after astrocytic activation ceased. In vivo, astrocytic activation enhanced memory allocation; i.e., it increased neuronal activity in a task-specific way only when coupled with learning, but not in home-caged mice. Furthermore, astrocytic activation using either a chemogenetic or an optogenetic tool during acquisition resulted in memory recall enhancement on the following day. Conversely, directly increasing neuronal activity resulted in dramatic memory impairment. Our findings that astrocytes induce plasticity and enhance memory may have important clinical implications for cognitive augmentation treatments.Entities:
Keywords: LTP; OptoXR; cFos; calcium imaging; chemogenetics; fear conditioning; hippocampus; memory allocation; miniature EPSCs; optogenetics
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Year: 2018 PMID: 29804835 DOI: 10.1016/j.cell.2018.05.002
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582