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Low-Dimensional Spatiotemporal Dynamics Underlie Cortex-wide Neural Activity.

ABSTRACT: Cognition arises from the dynamic flow of neural activity through the brain. To capture these dynamics, we used mesoscale calcium imaging to record neural activity across the dorsal cortex of awake mice. We found that the large majority of variance in cortex-wide activity (∼75%) could be explained by a limited set of ∼14 "motifs" of neural activity. Each motif captured a unique spatiotemporal pattern of neural activity across the cortex. These motifs generalized across animals and were seen in multiple behavioral environments. Motif expression differed across behavioral states, and specific motifs were engaged by sensory processing, suggesting the motifs reflect core cortical computations. Together, our results show that cortex-wide neural activity is highly dynamic but that these dynamics are restricted to a low-dimensional set of motifs, potentially allowing for efficient control of behavior.

SUBMITTER: MacDowell CJ

PROVIDER: S-EPMC7375907 | biostudies-literature | 2020 Jul

REPOSITORIES: biostudies-literature

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Low-Dimensional Spatiotemporal Dynamics Underlie Cortex-wide Neural Activity.

MacDowell Camden J CJ Buschman Timothy J TJ

Current biology : CB 20200528 14

Cognition arises from the dynamic flow of neural activity through the brain. To capture these dynamics, we used mesoscale calcium imaging to record neural activity across the dorsal cortex of awake mice. We found that the large majority of variance in cortex-wide activity (∼75%) could be explained by a limited set of ∼14 "motifs" of neural activity. Each motif captured a unique spatiotemporal pattern of neural activity across the cortex. These motifs generalized across animals and were seen in m ...[more]

PMID: 32470366

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Project description:Objective. Electrical recordings of neural activity from brain surface have been widely employed in basic neuroscience research and clinical practice for investigations of neural circuit functions, brain-computer interfaces, and treatments for neurological disorders. Traditionally, these surface potentials have been believed to mainly reflect local neural activity. It is not known how informative the locally recorded surface potentials are for the neural activities across multiple cortical regions.Approach. To investigate that, we perform simultaneous local electrical recording and wide-field calcium imaging in awake head-fixed mice. Using a recurrent neural network model, we try to decode the calcium fluorescence activity of multiple cortical regions from local electrical recordings.Main results. The mean activity of different cortical regions could be decoded from locally recorded surface potentials. Also, each frequency band of surface potentials differentially encodes activities from multiple cortical regions so that including all the frequency bands in the decoding model gives the highest decoding performance. Despite the close spacing between recording channels, surface potentials from different channels provide complementary information about the large-scale cortical activity and the decoding performance continues to improve as more channels are included. Finally, we demonstrate the successful decoding of whole dorsal cortex activity at pixel-level using locally recorded surface potentials.Significance. These results show that the locally recorded surface potentials indeed contain rich information of the large-scale neural activities, which could be further demixed to recover the neural activity across individual cortical regions. In the future, our cross-modality inference approach could be adapted to virtually reconstruct cortex-wide brain activity, greatly expanding the spatial reach of surface electrical recordings without increasing invasiveness. Furthermore, it could be used to facilitate imaging neural activity across the whole cortex in freely moving animals, without requirement of head-fixed microscopy configurations.

Dataset Information

Low-Dimensional Spatiotemporal Dynamics Underlie Cortex-wide Neural Activity.

Publications

Low-Dimensional Spatiotemporal Dynamics Underlie Cortex-wide Neural Activity.

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