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Spiking in primary somatosensory cortex during natural whisking in awake head-restrained rats is cell-type specific.

ABSTRACT: Sensation involves active movement of sensory organs, but it remains unknown how position or movement of sensory organs is encoded in cortex. In the rat whisker system, each whisker is represented by an individual cortical (barrel) column. Here, we quantified in awake, head-fixed rats the impact of natural whisker movements on action potential frequencies of single (identified) neurons located in different layers of somatosensory (barrel) cortex. In all layers, we found only weak correlations between spiking and whisker position or velocity. Conversely, whisking significantly increased spiking rate in a subset of neurons located preferentially in layer 5A. This finding suggests that whisker movement could be encoded by population responses of neurons within all layers and by single slender-tufted pyramids in layer 5A.

SUBMITTER: de Kock CP

PROVIDER: S-EPMC2752569 | biostudies-literature | 2009 Sep

REPOSITORIES: biostudies-literature

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Spiking in primary somatosensory cortex during natural whisking in awake head-restrained rats is cell-type specific.

de Kock Christiaan P J CP Sakmann Bert B

Proceedings of the National Academy of Sciences of the United States of America 20090904 38

Sensation involves active movement of sensory organs, but it remains unknown how position or movement of sensory organs is encoded in cortex. In the rat whisker system, each whisker is represented by an individual cortical (barrel) column. Here, we quantified in awake, head-fixed rats the impact of natural whisker movements on action potential frequencies of single (identified) neurons located in different layers of somatosensory (barrel) cortex. In all layers, we found only weak correlations be ...[more]

PMID: 19805318

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Project description:Lateralization is a hallmark of somatosensory processing in the mammalian brain. However, in addition to their contralateral representation, unilateral tactile stimuli also modulate neuronal activity in somatosensory cortices of the ipsilateral hemisphere. The cellular organization and functional role of these ipsilateral stimulus responses in awake somatosensory cortices, especially regarding stimulus coding, are unknown. Here, we targeted silicon probe recordings to the vibrissa region of primary (S1) and secondary (S2) somatosensory cortex of awake head-fixed mice of either sex while delivering ipsilateral and contralateral whisker stimuli. Ipsilateral stimuli drove larger and more reliable responses in S2 than in S1, and activated a larger fraction of stimulus-responsive neurons. Ipsilateral stimulus-responsive neurons were rare in layer 4 of S1, but were located in equal proportion across all layers in S2. Linear classifier analyses further revealed that decoding of the ipsilateral stimulus was more accurate in S2 than S1, whereas S1 decoded contralateral stimuli most accurately. These results reveal substantial encoding of ipsilateral stimuli in S1 and especially S2, consistent with the hypothesis that higher cortical areas may integrate tactile inputs across larger portions of space, spanning both sides of the body.SIGNIFICANCE STATEMENT Tactile information obtained by one side of the body is represented in the activity of neurons of the opposite brain hemisphere. However, unilateral tactile stimulation also modulates neuronal activity in the other, or ipsilateral, brain hemisphere. This ipsilateral activity may play an important role in the representation and processing of tactile information, in particular when the sense of touch involves both sides of the body. Our work in the whisker system of awake mice reveals that neocortical ipsilateral activity, in particular that of deep layer excitatory neurons of secondary somatosensory cortex (S2), contains information about the presence and the velocity of unilateral tactile stimuli, which supports a key role for S2 in integrating tactile information across both body sides.

Dataset Information

Spiking in primary somatosensory cortex during natural whisking in awake head-restrained rats is cell-type specific.

Publications

Spiking in primary somatosensory cortex during natural whisking in awake head-restrained rats is cell-type specific.

Similar Datasets

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