Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
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
_version_ 1782507619175366656
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
work_keys_str_mv AT sternfeldmatthewj speedandsegmentationcontrolmechanismscharacterizedinrhythmicallyactivecircuitscreatedfromspinalneuronsproducedfromgeneticallytaggedembryonicstemcells
AT hinckleychristophera speedandsegmentationcontrolmechanismscharacterizedinrhythmicallyactivecircuitscreatedfromspinalneuronsproducedfromgeneticallytaggedembryonicstemcells
AT mooreniallj speedandsegmentationcontrolmechanismscharacterizedinrhythmicallyactivecircuitscreatedfromspinalneuronsproducedfromgeneticallytaggedembryonicstemcells
AT pankratzmatthewt speedandsegmentationcontrolmechanismscharacterizedinrhythmicallyactivecircuitscreatedfromspinalneuronsproducedfromgeneticallytaggedembryonicstemcells
AT hildekathrynl speedandsegmentationcontrolmechanismscharacterizedinrhythmicallyactivecircuitscreatedfromspinalneuronsproducedfromgeneticallytaggedembryonicstemcells
AT driscollshawnp speedandsegmentationcontrolmechanismscharacterizedinrhythmicallyactivecircuitscreatedfromspinalneuronsproducedfromgeneticallytaggedembryonicstemcells
AT hayashimarito speedandsegmentationcontrolmechanismscharacterizedinrhythmicallyactivecircuitscreatedfromspinalneuronsproducedfromgeneticallytaggedembryonicstemcells
AT aminneald speedandsegmentationcontrolmechanismscharacterizedinrhythmicallyactivecircuitscreatedfromspinalneuronsproducedfromgeneticallytaggedembryonicstemcells
AT bonanomidario speedandsegmentationcontrolmechanismscharacterizedinrhythmicallyactivecircuitscreatedfromspinalneuronsproducedfromgeneticallytaggedembryonicstemcells
AT giffordwesleyd speedandsegmentationcontrolmechanismscharacterizedinrhythmicallyactivecircuitscreatedfromspinalneuronsproducedfromgeneticallytaggedembryonicstemcells
AT sharmakamal speedandsegmentationcontrolmechanismscharacterizedinrhythmicallyactivecircuitscreatedfromspinalneuronsproducedfromgeneticallytaggedembryonicstemcells
AT gouldingmartyn speedandsegmentationcontrolmechanismscharacterizedinrhythmicallyactivecircuitscreatedfromspinalneuronsproducedfromgeneticallytaggedembryonicstemcells
AT pfaffsamuell speedandsegmentationcontrolmechanismscharacterizedinrhythmicallyactivecircuitscreatedfromspinalneuronsproducedfromgeneticallytaggedembryonicstemcells