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Role of Synchronous Activation of Cerebellar Purkinje Cell Ensembles in Multi-joint Movement Control

It is a longstanding question in neuroscience how elaborate multi-joint movements are coordinated coherently. Microzones of cerebellar Purkinje cells (PCs) are thought to mediate this coordination by controlling the timing of particular motor domains. However, it remains to be elucidated to what ext...

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Autores principales: Hoogland, Tycho M., De Gruijl, Jornt R., Witter, Laurens, Canto, Cathrin B., De Zeeuw, Chris I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4425462/
https://www.ncbi.nlm.nih.gov/pubmed/25843032
http://dx.doi.org/10.1016/j.cub.2015.03.009
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author Hoogland, Tycho M.
De Gruijl, Jornt R.
Witter, Laurens
Canto, Cathrin B.
De Zeeuw, Chris I.
author_facet Hoogland, Tycho M.
De Gruijl, Jornt R.
Witter, Laurens
Canto, Cathrin B.
De Zeeuw, Chris I.
author_sort Hoogland, Tycho M.
collection PubMed
description It is a longstanding question in neuroscience how elaborate multi-joint movements are coordinated coherently. Microzones of cerebellar Purkinje cells (PCs) are thought to mediate this coordination by controlling the timing of particular motor domains. However, it remains to be elucidated to what extent motor coordination deficits can be correlated with abnormalities in coherent activity within these microzones and to what extent artificially evoked synchronous activity within PC ensembles can elicit multi-joint motor behavior. To study PC ensemble correlates of limb, trunk, and tail movements, we developed a transparent disk treadmill that allows quantitative readout of locomotion and posture parameters in head-fixed mice and simultaneous cellular-resolution imaging and/or optogenetic manipulation. We show that PC ensembles in the ataxic and dystonic mouse mutant tottering have a reduced level of complex spike co-activation, which is delayed relative to movement onset and co-occurs with prolonged swing duration and reduced phase coupling of limb movements as well as with enlarged deflections of body-axis and tail movements. Using optogenetics to increase simple spike rate in PC ensembles, we find that preferred locomotion and posture patterns can be elicited or perturbed depending on the behavioral state. At rest, preferred sequences of limb movements can be elicited, whereas during locomotion, preferred gait-inhibition patterns are evoked. Our findings indicate that synchronous activation of PC ensembles can facilitate initiation and coordination of limb and trunk movements, presumably by tuning downstream systems involved in the execution of behavioral patterns.
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spelling pubmed-44254622015-05-13 Role of Synchronous Activation of Cerebellar Purkinje Cell Ensembles in Multi-joint Movement Control Hoogland, Tycho M. De Gruijl, Jornt R. Witter, Laurens Canto, Cathrin B. De Zeeuw, Chris I. Curr Biol Article It is a longstanding question in neuroscience how elaborate multi-joint movements are coordinated coherently. Microzones of cerebellar Purkinje cells (PCs) are thought to mediate this coordination by controlling the timing of particular motor domains. However, it remains to be elucidated to what extent motor coordination deficits can be correlated with abnormalities in coherent activity within these microzones and to what extent artificially evoked synchronous activity within PC ensembles can elicit multi-joint motor behavior. To study PC ensemble correlates of limb, trunk, and tail movements, we developed a transparent disk treadmill that allows quantitative readout of locomotion and posture parameters in head-fixed mice and simultaneous cellular-resolution imaging and/or optogenetic manipulation. We show that PC ensembles in the ataxic and dystonic mouse mutant tottering have a reduced level of complex spike co-activation, which is delayed relative to movement onset and co-occurs with prolonged swing duration and reduced phase coupling of limb movements as well as with enlarged deflections of body-axis and tail movements. Using optogenetics to increase simple spike rate in PC ensembles, we find that preferred locomotion and posture patterns can be elicited or perturbed depending on the behavioral state. At rest, preferred sequences of limb movements can be elicited, whereas during locomotion, preferred gait-inhibition patterns are evoked. Our findings indicate that synchronous activation of PC ensembles can facilitate initiation and coordination of limb and trunk movements, presumably by tuning downstream systems involved in the execution of behavioral patterns. Cell Press 2015-05-04 /pmc/articles/PMC4425462/ /pubmed/25843032 http://dx.doi.org/10.1016/j.cub.2015.03.009 Text en © 2015 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Hoogland, Tycho M.
De Gruijl, Jornt R.
Witter, Laurens
Canto, Cathrin B.
De Zeeuw, Chris I.
Role of Synchronous Activation of Cerebellar Purkinje Cell Ensembles in Multi-joint Movement Control
title Role of Synchronous Activation of Cerebellar Purkinje Cell Ensembles in Multi-joint Movement Control
title_full Role of Synchronous Activation of Cerebellar Purkinje Cell Ensembles in Multi-joint Movement Control
title_fullStr Role of Synchronous Activation of Cerebellar Purkinje Cell Ensembles in Multi-joint Movement Control
title_full_unstemmed Role of Synchronous Activation of Cerebellar Purkinje Cell Ensembles in Multi-joint Movement Control
title_short Role of Synchronous Activation of Cerebellar Purkinje Cell Ensembles in Multi-joint Movement Control
title_sort role of synchronous activation of cerebellar purkinje cell ensembles in multi-joint movement control
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4425462/
https://www.ncbi.nlm.nih.gov/pubmed/25843032
http://dx.doi.org/10.1016/j.cub.2015.03.009
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