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The whisking oscillator circuit

Author

Listed:
  • Jun Takatoh

    (McGovern Institute for Brain Research, Massachusetts Institute of Technology
    Duke University)

  • Vincent Prevosto

    (McGovern Institute for Brain Research, Massachusetts Institute of Technology
    Duke University)

  • P. M. Thompson

    (McGovern Institute for Brain Research, Massachusetts Institute of Technology
    Duke University)

  • Jinghao Lu

    (McGovern Institute for Brain Research, Massachusetts Institute of Technology
    Duke University)

  • Leeyup Chung

    (Boston Children’s Hospital
    Harvard Medical School
    Harvard Medical School)

  • Andrew Harrahill

    (McGovern Institute for Brain Research, Massachusetts Institute of Technology)

  • Shun Li

    (Duke University)

  • Shengli Zhao

    (Duke University)

  • Zhigang He

    (Boston Children’s Hospital
    Harvard Medical School
    Harvard Medical School)

  • David Golomb

    (Ben Gurion University
    Ben Gurion University
    Ben Gurion University)

  • David Kleinfeld

    (University of California at San Diego
    University of California at San Diego)

  • Fan Wang

    (McGovern Institute for Brain Research, Massachusetts Institute of Technology
    Duke University)

Abstract

Central oscillators are primordial neural circuits that generate and control rhythmic movements1,2. Mechanistic understanding of these circuits requires genetic identification of the oscillator neurons and their synaptic connections to enable targeted electrophysiological recording and causal manipulation during behaviours. However, such targeting remains a challenge with mammalian systems. Here we delimit the oscillator circuit that drives rhythmic whisking—a motor action that is central to foraging and active sensing in rodents3,4. We found that the whisking oscillator consists of parvalbumin-expressing inhibitory neurons located in the vibrissa intermediate reticular nucleus (vIRtPV) in the brainstem. vIRtPV neurons receive descending excitatory inputs and form recurrent inhibitory connections among themselves. Silencing vIRtPV neurons eliminated rhythmic whisking and resulted in sustained vibrissae protraction. In vivo recording of opto-tagged vIRtPV neurons in awake mice showed that these cells spike tonically when animals are at rest, and transition to rhythmic bursting at the onset of whisking, suggesting that rhythm generation is probably the result of network dynamics, as opposed to intrinsic cellular properties. Notably, ablating inhibitory synaptic inputs to vIRtPV neurons quenched their rhythmic bursting, impaired the tonic-to-bursting transition and abolished regular whisking. Thus, the whisking oscillator is an all-inhibitory network and recurrent synaptic inhibition has a key role in its rhythmogenesis.

Suggested Citation

  • Jun Takatoh & Vincent Prevosto & P. M. Thompson & Jinghao Lu & Leeyup Chung & Andrew Harrahill & Shun Li & Shengli Zhao & Zhigang He & David Golomb & David Kleinfeld & Fan Wang, 2022. "The whisking oscillator circuit," Nature, Nature, vol. 609(7927), pages 560-568, September.
  • Handle: RePEc:nat:nature:v:609:y:2022:i:7927:d:10.1038_s41586-022-05144-8
    DOI: 10.1038/s41586-022-05144-8
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    Cited by:

    1. Suma Chinta & Scott R. Pluta, 2023. "Neural mechanisms for the localization of unexpected external motion," Nature Communications, Nature, vol. 14(1), pages 1-13, December.

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