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Speed and segmentation control mechanisms characterized in rhythmically-active circuits created from spinal neurons produced from genetically-tagged embryonic stem cells
Flexible neural networks, such as the interconnected spinal neurons that control distinct motor actions, can switch their activity to produce different behaviors. Both excitatory (E) and inhibitory (I) spinal neurons are necessary for motor behavior, but the influence of recruiting different ratios...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5308898/ https://www.ncbi.nlm.nih.gov/pubmed/28195039 http://dx.doi.org/10.7554/eLife.21540 |
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author | Sternfeld, Matthew J Hinckley, Christopher A Moore, Niall J Pankratz, Matthew T Hilde, Kathryn L Driscoll, Shawn P Hayashi, Marito Amin, Neal D Bonanomi, Dario Gifford, Wesley D Sharma, Kamal Goulding, Martyn Pfaff, Samuel L |
author_facet | Sternfeld, Matthew J Hinckley, Christopher A Moore, Niall J Pankratz, Matthew T Hilde, Kathryn L Driscoll, Shawn P Hayashi, Marito Amin, Neal D Bonanomi, Dario Gifford, Wesley D Sharma, Kamal Goulding, Martyn Pfaff, Samuel L |
author_sort | Sternfeld, Matthew J |
collection | PubMed |
description | Flexible neural networks, such as the interconnected spinal neurons that control distinct motor actions, can switch their activity to produce different behaviors. Both excitatory (E) and inhibitory (I) spinal neurons are necessary for motor behavior, but the influence of recruiting different ratios of E-to-I cells remains unclear. We constructed synthetic microphysical neural networks, called circuitoids, using precise combinations of spinal neuron subtypes derived from mouse stem cells. Circuitoids of purified excitatory interneurons were sufficient to generate oscillatory bursts with properties similar to in vivo central pattern generators. Inhibitory V1 neurons provided dual layers of regulation within excitatory rhythmogenic networks - they increased the rhythmic burst frequency of excitatory V3 neurons, and segmented excitatory motor neuron activity into sub-networks. Accordingly, the speed and pattern of spinal circuits that underlie complex motor behaviors may be regulated by quantitatively gating the intra-network cellular activity ratio of E-to-I neurons. DOI: http://dx.doi.org/10.7554/eLife.21540.001 |
format | Online Article Text |
id | pubmed-5308898 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-53088982017-02-15 Speed and segmentation control mechanisms characterized in rhythmically-active circuits created from spinal neurons produced from genetically-tagged embryonic stem cells Sternfeld, Matthew J Hinckley, Christopher A Moore, Niall J Pankratz, Matthew T Hilde, Kathryn L Driscoll, Shawn P Hayashi, Marito Amin, Neal D Bonanomi, Dario Gifford, Wesley D Sharma, Kamal Goulding, Martyn Pfaff, Samuel L eLife Cell Biology Flexible neural networks, such as the interconnected spinal neurons that control distinct motor actions, can switch their activity to produce different behaviors. Both excitatory (E) and inhibitory (I) spinal neurons are necessary for motor behavior, but the influence of recruiting different ratios of E-to-I cells remains unclear. We constructed synthetic microphysical neural networks, called circuitoids, using precise combinations of spinal neuron subtypes derived from mouse stem cells. Circuitoids of purified excitatory interneurons were sufficient to generate oscillatory bursts with properties similar to in vivo central pattern generators. Inhibitory V1 neurons provided dual layers of regulation within excitatory rhythmogenic networks - they increased the rhythmic burst frequency of excitatory V3 neurons, and segmented excitatory motor neuron activity into sub-networks. Accordingly, the speed and pattern of spinal circuits that underlie complex motor behaviors may be regulated by quantitatively gating the intra-network cellular activity ratio of E-to-I neurons. DOI: http://dx.doi.org/10.7554/eLife.21540.001 eLife Sciences Publications, Ltd 2017-02-14 /pmc/articles/PMC5308898/ /pubmed/28195039 http://dx.doi.org/10.7554/eLife.21540 Text en © 2017, Sternfeld et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Sternfeld, Matthew J Hinckley, Christopher A Moore, Niall J Pankratz, Matthew T Hilde, Kathryn L Driscoll, Shawn P Hayashi, Marito Amin, Neal D Bonanomi, Dario Gifford, Wesley D Sharma, Kamal Goulding, Martyn Pfaff, Samuel L Speed and segmentation control mechanisms characterized in rhythmically-active circuits created from spinal neurons produced from genetically-tagged embryonic stem cells |
title | Speed and segmentation control mechanisms characterized in rhythmically-active circuits created from spinal neurons produced from genetically-tagged embryonic stem cells |
title_full | Speed and segmentation control mechanisms characterized in rhythmically-active circuits created from spinal neurons produced from genetically-tagged embryonic stem cells |
title_fullStr | Speed and segmentation control mechanisms characterized in rhythmically-active circuits created from spinal neurons produced from genetically-tagged embryonic stem cells |
title_full_unstemmed | Speed and segmentation control mechanisms characterized in rhythmically-active circuits created from spinal neurons produced from genetically-tagged embryonic stem cells |
title_short | Speed and segmentation control mechanisms characterized in rhythmically-active circuits created from spinal neurons produced from genetically-tagged embryonic stem cells |
title_sort | speed and segmentation control mechanisms characterized in rhythmically-active circuits created from spinal neurons produced from genetically-tagged embryonic stem cells |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5308898/ https://www.ncbi.nlm.nih.gov/pubmed/28195039 http://dx.doi.org/10.7554/eLife.21540 |
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