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Activity‐dependent redistribution of Kv2.1 ion channels on rat spinal motoneurons
Homeostatic plasticity occurs through diverse cellular and synaptic mechanisms, and extensive investigations over the preceding decade have established Kv2.1 ion channels as key homeostatic regulatory elements in several central neuronal systems. As in these cellular systems, Kv2.1 channels in spina...
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/PMC5358001/ https://www.ncbi.nlm.nih.gov/pubmed/27884958 http://dx.doi.org/10.14814/phy2.13039 |
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author | Romer, Shannon H. Deardorff, Adam S. Fyffe, Robert E. W. |
author_facet | Romer, Shannon H. Deardorff, Adam S. Fyffe, Robert E. W. |
author_sort | Romer, Shannon H. |
collection | PubMed |
description | Homeostatic plasticity occurs through diverse cellular and synaptic mechanisms, and extensive investigations over the preceding decade have established Kv2.1 ion channels as key homeostatic regulatory elements in several central neuronal systems. As in these cellular systems, Kv2.1 channels in spinal motoneurons (MNs) localize within large somatic membrane clusters. However, their role in regulating motoneuron activity is not fully established in vivo. We have previously demonstrated marked Kv2.1 channel redistribution in MNs following in vitro glutamate application and in vivo peripheral nerve injury (Romer et al., 2014, Brain Research, 1547:1–15). Here, we extend these findings through the novel use of a fully intact, in vivo rat preparation to show that Kv2.1 ion channels in lumbar MNs rapidly and reversibly redistribute throughout the somatic membrane following 10 min of electrophysiological sensory and/or motor nerve stimulation. These data establish that Kv2.1 channels are remarkably responsive in vivo to electrically evoked and synaptically driven action potentials in MNs, and strongly implicate motoneuron Kv2.1 channels in the rapid homeostatic response to altered neuronal activity. |
format | Online Article Text |
id | pubmed-5358001 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53580012017-03-22 Activity‐dependent redistribution of Kv2.1 ion channels on rat spinal motoneurons Romer, Shannon H. Deardorff, Adam S. Fyffe, Robert E. W. Physiol Rep Original Research Homeostatic plasticity occurs through diverse cellular and synaptic mechanisms, and extensive investigations over the preceding decade have established Kv2.1 ion channels as key homeostatic regulatory elements in several central neuronal systems. As in these cellular systems, Kv2.1 channels in spinal motoneurons (MNs) localize within large somatic membrane clusters. However, their role in regulating motoneuron activity is not fully established in vivo. We have previously demonstrated marked Kv2.1 channel redistribution in MNs following in vitro glutamate application and in vivo peripheral nerve injury (Romer et al., 2014, Brain Research, 1547:1–15). Here, we extend these findings through the novel use of a fully intact, in vivo rat preparation to show that Kv2.1 ion channels in lumbar MNs rapidly and reversibly redistribute throughout the somatic membrane following 10 min of electrophysiological sensory and/or motor nerve stimulation. These data establish that Kv2.1 channels are remarkably responsive in vivo to electrically evoked and synaptically driven action potentials in MNs, and strongly implicate motoneuron Kv2.1 channels in the rapid homeostatic response to altered neuronal activity. John Wiley and Sons Inc. 2016-11-24 /pmc/articles/PMC5358001/ /pubmed/27884958 http://dx.doi.org/10.14814/phy2.13039 Text en © 2016 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American 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 | Original Research Romer, Shannon H. Deardorff, Adam S. Fyffe, Robert E. W. Activity‐dependent redistribution of Kv2.1 ion channels on rat spinal motoneurons |
title | Activity‐dependent redistribution of Kv2.1 ion channels on rat spinal motoneurons |
title_full | Activity‐dependent redistribution of Kv2.1 ion channels on rat spinal motoneurons |
title_fullStr | Activity‐dependent redistribution of Kv2.1 ion channels on rat spinal motoneurons |
title_full_unstemmed | Activity‐dependent redistribution of Kv2.1 ion channels on rat spinal motoneurons |
title_short | Activity‐dependent redistribution of Kv2.1 ion channels on rat spinal motoneurons |
title_sort | activity‐dependent redistribution of kv2.1 ion channels on rat spinal motoneurons |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5358001/ https://www.ncbi.nlm.nih.gov/pubmed/27884958 http://dx.doi.org/10.14814/phy2.13039 |
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