Cortex-wide spatiotemporal motifs of theta oscillations are coupled to freely moving behavior

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Abstract

Multisensory information is combined across the cortex and assimilated into the continuous production of ongoing behavior. In the hippocampus, theta oscillations (4-12 Hz) radiate as large-scale traveling waves, and serve as a scaffold for neuronal ensembles of multisensory information involved in memory and movement-related processing. An extension of such an encoding framework across the neocortex could similarly serve to bind disparate multisensory signals into ongoing, coherent, phase-coded processes. Whether the neocortex exhibits unique large-scale traveling waves distinct from that of the hippocampus however, remains unknown. Here, using cortex-wide electrocorticography in freely moving mice, we find that theta oscillations are organized into bilaterally-symmetric spatiotemporal “modes” that span virtually the entire neocortex. The dominant mode (Mode 1) is a divergent traveling wave that originates from retrosplenial cortex and whose amplitude correlates with mouse speed. Secondary modes are asynchronous spiral waves centered over primary somatosensory cortex (Modes 2 & 3), which become prominent during rapid drops in amplitude and synchrony (null spikes) and which underlie a phase reset of Mode 1. These structured cortex-wide traveling waves may provide a scaffold for large-scale phase-coding that allows the binding of multisensory information across all the regions of the cortex.

Bulleted list of key results

  • Cortical theta oscillations are organized into bilaterally-symmetric spatiotemporal modes that span the neocortex.

  • The dominant mode appears as a divergent traveling wave that originates in retrosplenial cortex and is correlated with mouse speed.

  • Secondary modes are asynchronous spiral waves centered over somatosensory cortex.

  • Secondary modes become prominent during transient drops in synchrony that underlie a phase reset of the dominant mode.

  • We hypothesize that spiral waves may provide a mechanism to exert large-scale phase separability, and assimilate information into ongoing multisensory processing across the neocortex.

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