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Labelling and optical erasure of synaptic memory traces in the motor cortex

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  • Akiko Hayashi-Takagi

    (Laboratory of Structural Physiology, Center for Disease Biology and Integrative Medicine, Faculty of Medicine, University of Tokyo
    PRESTO, Japan Science and Technology Agency)

  • Sho Yagishita

    (Laboratory of Structural Physiology, Center for Disease Biology and Integrative Medicine, Faculty of Medicine, University of Tokyo
    CREST, Japan Science and Technology Agency)

  • Mayumi Nakamura

    (Laboratory of Structural Physiology, Center for Disease Biology and Integrative Medicine, Faculty of Medicine, University of Tokyo)

  • Fukutoshi Shirai

    (Laboratory of Structural Physiology, Center for Disease Biology and Integrative Medicine, Faculty of Medicine, University of Tokyo)

  • Yi I. Wu

    (Center for Cell Analysis and Modeling, University of Connecticut Health Center, Farmington, Connecticut 06032, USA)

  • Amanda L. Loshbaugh

    (Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, North Carolina 27599, USA
    University of North Carolina, Chapel Hill, North Carolina 27599, USA)

  • Brian Kuhlman

    (Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, North Carolina 27599, USA
    University of North Carolina, Chapel Hill, North Carolina 27599, USA)

  • Klaus M. Hahn

    (Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, North Carolina 27599, USA
    University of North Carolina, Chapel Hill, North Carolina 27599, USA)

  • Haruo Kasai

    (Laboratory of Structural Physiology, Center for Disease Biology and Integrative Medicine, Faculty of Medicine, University of Tokyo
    CREST, Japan Science and Technology Agency)

Abstract

Dendritic spines are the major loci of synaptic plasticity and are considered as possible structural correlates of memory. Nonetheless, systematic manipulation of specific subsets of spines in the cortex has been unattainable, and thus, the link between spines and memory has been correlational. We developed a novel synaptic optoprobe, AS-PaRac1 (activated synapse targeting photoactivatable Rac1), that can label recently potentiated spines specifically, and induce the selective shrinkage of AS-PaRac1-containing spines. In vivo imaging of AS-PaRac1 revealed that a motor learning task induced substantial synaptic remodelling in a small subset of neurons. The acquired motor learning was disrupted by the optical shrinkage of the potentiated spines, whereas it was not affected by the identical manipulation of spines evoked by a distinct motor task in the same cortical region. Taken together, our results demonstrate that a newly acquired motor skill depends on the formation of a task-specific dense synaptic ensemble.

Suggested Citation

  • Akiko Hayashi-Takagi & Sho Yagishita & Mayumi Nakamura & Fukutoshi Shirai & Yi I. Wu & Amanda L. Loshbaugh & Brian Kuhlman & Klaus M. Hahn & Haruo Kasai, 2015. "Labelling and optical erasure of synaptic memory traces in the motor cortex," Nature, Nature, vol. 525(7569), pages 333-338, September.
  • Handle: RePEc:nat:nature:v:525:y:2015:i:7569:d:10.1038_nature15257
    DOI: 10.1038/nature15257
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    Cited by:

    1. Rodrigo Ordoñez Sierra & Lizeth Katherine Pedraza & Lívia Barcsai & Andrea Pejin & Qun Li & Gábor Kozák & Yuichi Takeuchi & Anett J. Nagy & Magor L. Lőrincz & Orrin Devinsky & György Buzsáki & Antal B, 2023. "Closed-loop brain stimulation augments fear extinction in male rats," Nature Communications, Nature, vol. 14(1), pages 1-14, December.
    2. Francesco Paolo Ulloa Severino & Oluwadamilola O. Lawal & Kristina Sakers & Shiyi Wang & Namsoo Kim & Alexander David Friedman & Sarah Anne Johnson & Chaichontat Sriworarat & Ryan H. Hughes & Scott H., 2023. "Training-induced circuit-specific excitatory synaptogenesis in mice is required for effort control," Nature Communications, Nature, vol. 14(1), pages 1-22, December.
    3. Christopher M. Kim & Arseny Finkelstein & Carson C. Chow & Karel Svoboda & Ran Darshan, 2023. "Distributing task-related neural activity across a cortical network through task-independent connections," Nature Communications, Nature, vol. 14(1), pages 1-21, December.
    4. Hang Zhou & Guo-Qiang Bi & Guosong Liu, 2024. "Intracellular magnesium optimizes transmission efficiency and plasticity of hippocampal synapses by reconfiguring their connectivity," Nature Communications, Nature, vol. 15(1), pages 1-20, December.
    5. Roman Dvorkin & Noam E Ziv, 2016. "Relative Contributions of Specific Activity Histories and Spontaneous Processes to Size Remodeling of Glutamatergic Synapses," PLOS Biology, Public Library of Science, vol. 14(10), pages 1-33, October.

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