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Thalamic control of sensory selection in divided attention

Author

Listed:
  • Ralf D. Wimmer

    (New York University Neuroscience Institute, New York University Langone Medical Center)

  • L. Ian Schmitt

    (New York University Neuroscience Institute, New York University Langone Medical Center)

  • Thomas J. Davidson

    (Stanford University)

  • Miho Nakajima

    (New York University Neuroscience Institute, New York University Langone Medical Center)

  • Karl Deisseroth

    (Stanford University
    Cracking the Neural Code Program, Stanford University
    Stanford University)

  • Michael M. Halassa

    (New York University Neuroscience Institute, New York University Langone Medical Center
    New York University Langone Medical Center
    Center for Neural Science, New York University)

Abstract

The authors trained mice to attend to or suppress vision based on behavioral context and show, through novel and established techniques, that changes in visual gain rely on tunable feedforward inhibition of visual thalamus via innervating thalamic reticular neurons; these findings introduce a subcortical model of attention in which modality-specific thalamic reticular subnetworks mediate top-down and context-dependent control of sensory selection.

Suggested Citation

  • Ralf D. Wimmer & L. Ian Schmitt & Thomas J. Davidson & Miho Nakajima & Karl Deisseroth & Michael M. Halassa, 2015. "Thalamic control of sensory selection in divided attention," Nature, Nature, vol. 526(7575), pages 705-709, October.
    • Handle: RePEc:nat:nature:v:526:y:2015:i:7575:d:10.1038_nature15398
    DOI: 10.1038/nature15398
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    Citations

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    Cited by:

    1. Maxime Lemieux & Narges Karimi & Frederic Bretzner, 2024. "Functional plasticity of glutamatergic neurons of medullary reticular nuclei after spinal cord injury in mice," Nature Communications, Nature, vol. 15(1), pages 1-15, December.
    2. Shinichiro Kira & Houman Safaai & Ari S. Morcos & Stefano Panzeri & Christopher D. Harvey, 2023. "A distributed and efficient population code of mixed selectivity neurons for flexible navigation decisions," Nature Communications, Nature, vol. 14(1), pages 1-28, December.
    3. Masato Tsuji & Yuto Nishizuka & Kazuo Emoto, 2023. "Threat gates visual aversion via theta activity in Tachykinergic neurons," Nature Communications, Nature, vol. 14(1), pages 1-17, December.
    4. Zhaoran Zhang & Edward Zagha, 2023. "Motor cortex gates distractor stimulus encoding in sensory cortex," Nature Communications, Nature, vol. 14(1), pages 1-17, December.
    5. Márton Albert Hajnal & Duy Tran & Michael Einstein & Mauricio Vallejo Martelo & Karen Safaryan & Pierre-Olivier Polack & Peyman Golshani & Gergő Orbán, 2023. "Continuous multiplexed population representations of task context in the mouse primary visual cortex," Nature Communications, Nature, vol. 14(1), pages 1-20, December.
    6. Gal Atlan & Noa Matosevich & Noa Peretz-Rivlin & Idit Marsh-Yvgi & Noam Zelinger & Eden Chen & Timna Kleinman & Noa Bleistein & Efrat Sheinbach & Maya Groysman & Yuval Nir & Ami Citri, 2024. "Claustrum neurons projecting to the anterior cingulate restrict engagement during sleep and behavior," Nature Communications, Nature, vol. 15(1), pages 1-14, December.
    7. Masashi Hasegawa & Ziyan Huang & Ricardo Paricio-Montesinos & Jan Gründemann, 2024. "Network state changes in sensory thalamus represent learned outcomes," Nature Communications, Nature, vol. 15(1), pages 1-14, December.
    8. Yihan Wang & Qian-Quan Sun, 2024. "A prefrontal motor circuit initiates persistent movement," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
    9. Matthijs N. Oude Lohuis & Jean L. Pie & Pietro Marchesi & Jorrit S. Montijn & Christiaan P. J. Kock & Cyriel M. A. Pennartz & Umberto Olcese, 2022. "Multisensory task demands temporally extend the causal requirement for visual cortex in perception," Nature Communications, Nature, vol. 13(1), pages 1-19, December.

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