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Parallel pathways from motor and somatosensory cortex for controlling whisker movements in mice

Mice can gather tactile sensory information by actively moving their whiskers to palpate objects in their immediate surroundings. Whisker sensory perception therefore requires integration of sensory and motor information, which occurs prominently in the neocortex. The signalling pathways from the ne...

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Autores principales: Sreenivasan, Varun, Karmakar, Kajari, Rijli, Filippo M, Petersen, Carl C H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4359021/
https://www.ncbi.nlm.nih.gov/pubmed/25476605
http://dx.doi.org/10.1111/ejn.12800
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author Sreenivasan, Varun
Karmakar, Kajari
Rijli, Filippo M
Petersen, Carl C H
author_facet Sreenivasan, Varun
Karmakar, Kajari
Rijli, Filippo M
Petersen, Carl C H
author_sort Sreenivasan, Varun
collection PubMed
description Mice can gather tactile sensory information by actively moving their whiskers to palpate objects in their immediate surroundings. Whisker sensory perception therefore requires integration of sensory and motor information, which occurs prominently in the neocortex. The signalling pathways from the neocortex for controlling whisker movements are currently poorly understood in mice. Here, we delineate two pathways, one originating from primary whisker somatosensory cortex (wS1) and the other from whisker motor cortex (wM1), that control qualitatively distinct movements of contralateral whiskers. Optogenetic stimulation of wS1 drove retraction of contralateral whiskers while stimulation of wM1 drove rhythmic whisker protraction. To map brainstem pathways connecting these cortical areas to whisker motor neurons, we used a combination of anterograde tracing using adenoassociated virus injected into neocortex and retrograde tracing using monosynaptic rabies virus injected into whisker muscles. Our data are consistent with wS1 driving whisker retraction by exciting glutamatergic premotor neurons in the rostral spinal trigeminal interpolaris nucleus, which in turn activate the motor neurons innervating the extrinsic retractor muscle nasolabialis. The rhythmic whisker protraction evoked by wM1 stimulation might be driven by excitation of excitatory and inhibitory premotor neurons in the brainstem reticular formation innervating both intrinsic and extrinsic muscles. Our data therefore begin to unravel the neuronal circuits linking the neocortex to whisker motor neurons.
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spelling pubmed-43590212015-03-19 Parallel pathways from motor and somatosensory cortex for controlling whisker movements in mice Sreenivasan, Varun Karmakar, Kajari Rijli, Filippo M Petersen, Carl C H Eur J Neurosci Neurosystems Mice can gather tactile sensory information by actively moving their whiskers to palpate objects in their immediate surroundings. Whisker sensory perception therefore requires integration of sensory and motor information, which occurs prominently in the neocortex. The signalling pathways from the neocortex for controlling whisker movements are currently poorly understood in mice. Here, we delineate two pathways, one originating from primary whisker somatosensory cortex (wS1) and the other from whisker motor cortex (wM1), that control qualitatively distinct movements of contralateral whiskers. Optogenetic stimulation of wS1 drove retraction of contralateral whiskers while stimulation of wM1 drove rhythmic whisker protraction. To map brainstem pathways connecting these cortical areas to whisker motor neurons, we used a combination of anterograde tracing using adenoassociated virus injected into neocortex and retrograde tracing using monosynaptic rabies virus injected into whisker muscles. Our data are consistent with wS1 driving whisker retraction by exciting glutamatergic premotor neurons in the rostral spinal trigeminal interpolaris nucleus, which in turn activate the motor neurons innervating the extrinsic retractor muscle nasolabialis. The rhythmic whisker protraction evoked by wM1 stimulation might be driven by excitation of excitatory and inhibitory premotor neurons in the brainstem reticular formation innervating both intrinsic and extrinsic muscles. Our data therefore begin to unravel the neuronal circuits linking the neocortex to whisker motor neurons. BlackWell Publishing Ltd 2015-02 2014-12-05 /pmc/articles/PMC4359021/ /pubmed/25476605 http://dx.doi.org/10.1111/ejn.12800 Text en © 2014 The Authors. European Journal of Neuroscience published by Federation of European Neuroscience Societies and John Wiley & Sons Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Neurosystems
Sreenivasan, Varun
Karmakar, Kajari
Rijli, Filippo M
Petersen, Carl C H
Parallel pathways from motor and somatosensory cortex for controlling whisker movements in mice
title Parallel pathways from motor and somatosensory cortex for controlling whisker movements in mice
title_full Parallel pathways from motor and somatosensory cortex for controlling whisker movements in mice
title_fullStr Parallel pathways from motor and somatosensory cortex for controlling whisker movements in mice
title_full_unstemmed Parallel pathways from motor and somatosensory cortex for controlling whisker movements in mice
title_short Parallel pathways from motor and somatosensory cortex for controlling whisker movements in mice
title_sort parallel pathways from motor and somatosensory cortex for controlling whisker movements in mice
topic Neurosystems
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4359021/
https://www.ncbi.nlm.nih.gov/pubmed/25476605
http://dx.doi.org/10.1111/ejn.12800
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