| Literature DB >> 33619256 |
Brittany C Clawson1, Emily J Pickup1, Amy Ensing1, Laura Geneseo1, James Shaver1, John Gonzalez-Amoretti2, Meiling Zhao1, A Kane York3, Femke Roig Kuhn1,4, Kevin Swift5, Jessy D Martinez1, Lijing Wang1, Sha Jiang1, Sara J Aton6.
Abstract
Learning-activated engram neurons play a critical role in memory recall. An untested hypothesis is that these same neurons play an instructive role in offline memory consolidation. Here we show that a visually-cued fear memory is consolidated during post-conditioning sleep in mice. We then use TRAP (targeted recombination in active populations) to genetically label or optogenetically manipulate primary visual cortex (V1) neurons responsive to the visual cue. Following fear conditioning, mice respond to activation of this visual engram population in a manner similar to visual presentation of fear cues. Cue-responsive neurons are selectively reactivated in V1 during post-conditioning sleep. Mimicking visual engram reactivation optogenetically leads to increased representation of the visual cue in V1. Optogenetic inhibition of the engram population during post-conditioning sleep disrupts consolidation of fear memory. We conclude that selective sleep-associated reactivation of learning-activated sensory populations serves as a necessary instructive mechanism for memory consolidation.Entities:
Mesh:
Year: 2021 PMID: 33619256 PMCID: PMC7900186 DOI: 10.1038/s41467-021-21471-2
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919