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Sparse and distributed cortical populations mediate sensorimotor integration
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SUMMARYTouch information is central to sensorimotor integration, yet little is known about how cortical touch and movement representations interact. Touch- and movement-related activity is present in both somatosensory and motor cortices, making both candidate sites for touch-motor interactions. We studied touch-motor interactions in layer 2/3 of the primary vibrissal somatosensory and motor cortices of behaving mice. Volumetric two-photon calcium imaging revealed robust responses to whisker touch, whisking, and licking in both areas. Touch activity was dominated by a sparse population of broadly tuned neurons responsive to multiple whiskers that exhibited longitudinal stability and disproportionately influenced interareal communication. Movement representations were similarly dominated by sparse, stable, reciprocally projecting populations. In both areas, many broadly tuned touch cells also produced robust licking or whisking responses. These touch-licking and touch-whisking neurons showed distinct dynamics suggestive of specific roles in shaping movement. Cortical touch-motor interactions are thus mediated by specialized populations of highly responsive, broadly tuned neurons.
Title: Sparse and distributed cortical populations mediate sensorimotor integration
Description:
SUMMARYTouch information is central to sensorimotor integration, yet little is known about how cortical touch and movement representations interact.
Touch- and movement-related activity is present in both somatosensory and motor cortices, making both candidate sites for touch-motor interactions.
We studied touch-motor interactions in layer 2/3 of the primary vibrissal somatosensory and motor cortices of behaving mice.
Volumetric two-photon calcium imaging revealed robust responses to whisker touch, whisking, and licking in both areas.
Touch activity was dominated by a sparse population of broadly tuned neurons responsive to multiple whiskers that exhibited longitudinal stability and disproportionately influenced interareal communication.
Movement representations were similarly dominated by sparse, stable, reciprocally projecting populations.
In both areas, many broadly tuned touch cells also produced robust licking or whisking responses.
These touch-licking and touch-whisking neurons showed distinct dynamics suggestive of specific roles in shaping movement.
Cortical touch-motor interactions are thus mediated by specialized populations of highly responsive, broadly tuned neurons.
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