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Dendritic, delayed, stochastic CaMKII activation in behavioural time scale plasticity

Author

Listed:
  • Anant Jain

    (Neuronal Signal Transduction Group, Max Planck Florida Institute for Neuroscience
    TCG CREST)

  • Yoshihisa Nakahata

    (Neuronal Signal Transduction Group, Max Planck Florida Institute for Neuroscience)

  • Tristano Pancani

    (Neuronal Signal Transduction Group, Max Planck Florida Institute for Neuroscience)

  • Tetsuya Watabe

    (Neuronal Signal Transduction Group, Max Planck Florida Institute for Neuroscience)

  • Polina Rusina

    (Neuronal Signal Transduction Group, Max Planck Florida Institute for Neuroscience)

  • Kelly South

    (Neuronal Signal Transduction Group, Max Planck Florida Institute for Neuroscience)

  • Kengo Adachi

    (Neuronal Signal Transduction Group, Max Planck Florida Institute for Neuroscience)

  • Long Yan

    (Neuronal Signal Transduction Group, Max Planck Florida Institute for Neuroscience)

  • Noriko Simorowski

    (W.M. Keck Structural Biology Laboratory, Cold Spring Harbor Laboratory)

  • Hiro Furukawa

    (W.M. Keck Structural Biology Laboratory, Cold Spring Harbor Laboratory)

  • Ryohei Yasuda

    (Neuronal Signal Transduction Group, Max Planck Florida Institute for Neuroscience)

Abstract

Behavioural time scale plasticity (BTSP) is non-Hebbian plasticity induced by integrating presynaptic and postsynaptic components separated by a behaviourally relevant time scale (seconds)1. BTSP in hippocampal CA1 neurons underlies place cell formation. However, the molecular mechanisms that enable synapse-specific plasticity on a behavioural time scale are unknown. Here we show that BTSP can be induced in a single dendritic spine using two-photon glutamate uncaging paired with postsynaptic current injection temporally separated by a behavioural time scale. Using an improved Ca2+/calmodulin-dependent kinase II (CaMKII) sensor, we did not detect CaMKII activation during this BTSP induction. Instead, we observed dendritic, delayed and stochastic CaMKII activation (DDSC) associated with Ca2+ influx and plateau potentials 10–100 s after BTSP induction. DDSC required both presynaptic and postsynaptic activity, which suggests that CaMKII can integrate these two signals. Also, optogenetically blocking CaMKII 15–30 s after the BTSP protocol inhibited synaptic potentiation, which indicated that DDSC is an essential mechanism of BTSP. IP3-dependent intracellular Ca2+ release facilitated both DDSC and BTSP. Thus, our study suggests that non-synapse-specific CaMKII activation provides an instructive signal with an extensive time window over tens of seconds during BTSP.

Suggested Citation

  • Anant Jain & Yoshihisa Nakahata & Tristano Pancani & Tetsuya Watabe & Polina Rusina & Kelly South & Kengo Adachi & Long Yan & Noriko Simorowski & Hiro Furukawa & Ryohei Yasuda, 2024. "Dendritic, delayed, stochastic CaMKII activation in behavioural time scale plasticity," Nature, Nature, vol. 635(8037), pages 151-159, November.
  • Handle: RePEc:nat:nature:v:635:y:2024:i:8037:d:10.1038_s41586-024-08021-8
    DOI: 10.1038/s41586-024-08021-8
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