IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v12y2021i1d10.1038_s41467-021-21471-2.html
   My bibliography  Save this article

Causal role for sleep-dependent reactivation of learning-activated sensory ensembles for fear memory consolidation

Author

Listed:
  • Brittany C. Clawson

    (University of Michigan)

  • Emily J. Pickup

    (University of Michigan)

  • Amy Ensing

    (University of Michigan)

  • Laura Geneseo

    (University of Michigan)

  • James Shaver

    (University of Michigan)

  • John Gonzalez-Amoretti

    (Recinto de Gurabo)

  • Meiling Zhao

    (University of Michigan)

  • A. Kane York

    (University of Michigan)

  • Femke Roig Kuhn

    (University of Michigan
    VU University)

  • Kevin Swift

    (University of Michigan)

  • Jessy D. Martinez

    (University of Michigan)

  • Lijing Wang

    (University of Michigan)

  • Sha Jiang

    (University of Michigan)

  • Sara J. Aton

    (University of Michigan)

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.

Suggested Citation

  • Brittany C. Clawson & Emily J. Pickup & Amy Ensing & Laura Geneseo & James Shaver & John Gonzalez-Amoretti & Meiling Zhao & A. Kane York & Femke Roig Kuhn & Kevin Swift & Jessy D. Martinez & Lijing Wa, 2021. "Causal role for sleep-dependent reactivation of learning-activated sensory ensembles for fear memory consolidation," Nature Communications, Nature, vol. 12(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-21471-2
    DOI: 10.1038/s41467-021-21471-2
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-021-21471-2
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-021-21471-2?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    Citations

    Citations are extracted by the CitEc Project, subscribe to its RSS feed for this item.
    as


    Cited by:

    1. Su Z. Hong & Lukas Mesik & Cooper D. Grossman & Jeremiah Y. Cohen & Boram Lee & Daniel Severin & Hey-Kyoung Lee & Johannes W. Hell & Alfredo Kirkwood, 2022. "Norepinephrine potentiates and serotonin depresses visual cortical responses by transforming eligibility traces," Nature Communications, Nature, vol. 13(1), pages 1-12, December.
    2. Ruijie Li & Junjie Huang & Longhui Li & Zhikai Zhao & Susu Liang & Shanshan Liang & Meng Wang & Xiang Liao & Jing Lyu & Zhenqiao Zhou & Sibo Wang & Wenjun Jin & Haiyang Chen & Damaris Holder & Hongban, 2023. "Holistic bursting cells store long-term memory in auditory cortex," Nature Communications, Nature, vol. 14(1), pages 1-14, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-21471-2. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.