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Active integration of glutamatergic input to the inferior olive generates bidirectional postsynaptic potentials
KEY POINTS: We establish experimental preparations for optogenetic investigation of glutamatergic input to the inferior olive. Neurones in the principal olivary nucleus receive monosynaptic extra‐somatic glutamatergic input from the neocortex. Glutamatergic inputs to neurones in the inferior olive g...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5309349/ https://www.ncbi.nlm.nih.gov/pubmed/27767209 http://dx.doi.org/10.1113/JP273424 |
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author | Garden, Derek L. F. Rinaldi, Arianna Nolan, Matthew F. |
author_facet | Garden, Derek L. F. Rinaldi, Arianna Nolan, Matthew F. |
author_sort | Garden, Derek L. F. |
collection | PubMed |
description | KEY POINTS: We establish experimental preparations for optogenetic investigation of glutamatergic input to the inferior olive. Neurones in the principal olivary nucleus receive monosynaptic extra‐somatic glutamatergic input from the neocortex. Glutamatergic inputs to neurones in the inferior olive generate bidirectional postsynaptic potentials (PSPs), with a fast excitatory component followed by a slower inhibitory component. Small conductance calcium‐activated potassium (SK) channels are required for the slow inhibitory component of glutamatergic PSPs and oppose temporal summation of inputs at intervals ≤ 20 ms. Active integration of synaptic input within the inferior olive may play a central role in control of olivo‐cerebellar climbing fibre signals. ABSTRACT: The inferior olive plays a critical role in motor coordination and learning by integrating diverse afferent signals to generate climbing fibre inputs to the cerebellar cortex. While it is well established that climbing fibre signals are important for motor coordination, the mechanisms by which neurones in the inferior olive integrate synaptic inputs and the roles of particular ion channels are unclear. Here, we test the hypothesis that neurones in the inferior olive actively integrate glutamatergic synaptic inputs. We demonstrate that optogenetically activated long‐range synaptic inputs to the inferior olive, including projections from the motor cortex, generate rapid excitatory potentials followed by slower inhibitory potentials. Synaptic projections from the motor cortex preferentially target the principal olivary nucleus. We show that inhibitory and excitatory components of the bidirectional synaptic potentials are dependent upon AMPA (GluA) receptors, are GABA(A) independent, and originate from the same presynaptic axons. Consistent with models that predict active integration of synaptic inputs by inferior olive neurones, we find that the inhibitory component is reduced by blocking large conductance calcium‐activated potassium channels with iberiotoxin, and is abolished by blocking small conductance calcium‐activated potassium channels with apamin. Summation of excitatory components of synaptic responses to inputs at intervals ≤ 20 ms is increased by apamin, suggesting a role for the inhibitory component of glutamatergic responses in temporal integration. Our results indicate that neurones in the inferior olive implement novel rules for synaptic integration and suggest new principles for the contribution of inferior olive neurones to coordinated motor behaviours. |
format | Online Article Text |
id | pubmed-5309349 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53093492017-02-22 Active integration of glutamatergic input to the inferior olive generates bidirectional postsynaptic potentials Garden, Derek L. F. Rinaldi, Arianna Nolan, Matthew F. J Physiol Neuroscience ‐ Cellular/Molecular KEY POINTS: We establish experimental preparations for optogenetic investigation of glutamatergic input to the inferior olive. Neurones in the principal olivary nucleus receive monosynaptic extra‐somatic glutamatergic input from the neocortex. Glutamatergic inputs to neurones in the inferior olive generate bidirectional postsynaptic potentials (PSPs), with a fast excitatory component followed by a slower inhibitory component. Small conductance calcium‐activated potassium (SK) channels are required for the slow inhibitory component of glutamatergic PSPs and oppose temporal summation of inputs at intervals ≤ 20 ms. Active integration of synaptic input within the inferior olive may play a central role in control of olivo‐cerebellar climbing fibre signals. ABSTRACT: The inferior olive plays a critical role in motor coordination and learning by integrating diverse afferent signals to generate climbing fibre inputs to the cerebellar cortex. While it is well established that climbing fibre signals are important for motor coordination, the mechanisms by which neurones in the inferior olive integrate synaptic inputs and the roles of particular ion channels are unclear. Here, we test the hypothesis that neurones in the inferior olive actively integrate glutamatergic synaptic inputs. We demonstrate that optogenetically activated long‐range synaptic inputs to the inferior olive, including projections from the motor cortex, generate rapid excitatory potentials followed by slower inhibitory potentials. Synaptic projections from the motor cortex preferentially target the principal olivary nucleus. We show that inhibitory and excitatory components of the bidirectional synaptic potentials are dependent upon AMPA (GluA) receptors, are GABA(A) independent, and originate from the same presynaptic axons. Consistent with models that predict active integration of synaptic inputs by inferior olive neurones, we find that the inhibitory component is reduced by blocking large conductance calcium‐activated potassium channels with iberiotoxin, and is abolished by blocking small conductance calcium‐activated potassium channels with apamin. Summation of excitatory components of synaptic responses to inputs at intervals ≤ 20 ms is increased by apamin, suggesting a role for the inhibitory component of glutamatergic responses in temporal integration. Our results indicate that neurones in the inferior olive implement novel rules for synaptic integration and suggest new principles for the contribution of inferior olive neurones to coordinated motor behaviours. John Wiley and Sons Inc. 2016-11-29 2017-02-15 /pmc/articles/PMC5309349/ /pubmed/27767209 http://dx.doi.org/10.1113/JP273424 Text en © 2016 The Authors. The Journal of Physiology published by John Wiley & Sons Ltd on behalf of The Physiological Society This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Neuroscience ‐ Cellular/Molecular Garden, Derek L. F. Rinaldi, Arianna Nolan, Matthew F. Active integration of glutamatergic input to the inferior olive generates bidirectional postsynaptic potentials |
title | Active integration of glutamatergic input to the inferior olive generates bidirectional postsynaptic potentials |
title_full | Active integration of glutamatergic input to the inferior olive generates bidirectional postsynaptic potentials |
title_fullStr | Active integration of glutamatergic input to the inferior olive generates bidirectional postsynaptic potentials |
title_full_unstemmed | Active integration of glutamatergic input to the inferior olive generates bidirectional postsynaptic potentials |
title_short | Active integration of glutamatergic input to the inferior olive generates bidirectional postsynaptic potentials |
title_sort | active integration of glutamatergic input to the inferior olive generates bidirectional postsynaptic potentials |
topic | Neuroscience ‐ Cellular/Molecular |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5309349/ https://www.ncbi.nlm.nih.gov/pubmed/27767209 http://dx.doi.org/10.1113/JP273424 |
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