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<p>Sensory perception requires the processing of stimuli from both sides of the body. Yet, how neurons bind stimulus information across the hemispheres to create a unified percept remains unknown. Here we perform large-scale recordings from neurons in the left and right primary somatosensory cortex (S1) in mice performing a task requiring active whisker touch to coordinate stimulus features across hemispheres. When mice touched reward-associated stimuli, their whiskers moved with greater bilateral symmetry, and synchronous spiking and enhanced spike–field coupling emerged between the hemispheres. This coordinated activity was absent in stimulus-matched naive animals, indicating that interhemispheric coupling involves a goal-directed, internal process. In S1 neurons, the addition of ipsilateral touch primarily facilitated the contralateral principal whisker response. This facilitation primarily emerged for reward-associated stimuli and was lost on trials where mice failed to respond. Silencing of callosal S1 signaling reduced bilateral facilitation and interhemispheric synchrony. These results reveal a state-dependent logic that augments the flow of tactile information through the corpus callosum.</p>

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Bilateral integration in somatosensory cortex is controlled by behavioral relevance

  • 期刊论文

  • 发表日期：

    2025年5月14日

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  • Hyein Park,
  • Hayagreev V. S. Keri,
  • Chaeyoung Yoo,
  • Chengyu Bi,
  • Scott R. Pluta

摘要

Sensory perception requires the processing of stimuli from both sides of the body. Yet, how neurons bind stimulus information across the hemispheres to create a unified percept remains unknown. Here we perform large-scale recordings from neurons in the left and right primary somatosensory cortex (S1) in mice performing a task requiring active whisker touch to coordinate stimulus features across hemispheres. When mice touched reward-associated stimuli, their whiskers moved with greater bilateral symmetry, and synchronous spiking and enhanced spike–field coupling emerged between the hemispheres. This coordinated activity was absent in stimulus-matched naive animals, indicating that interhemispheric coupling involves a goal-directed, internal process. In S1 neurons, the addition of ipsilateral touch primarily facilitated the contralateral principal whisker response. This facilitation primarily emerged for reward-associated stimuli and was lost on trials where mice failed to respond. Silencing of callosal S1 signaling reduced bilateral facilitation and interhemispheric synchrony. These results reveal a state-dependent logic that augments the flow of tactile information through the corpus callosum.