Spinal Shox2 interneuron interconnectivity related to function and development

Neuronal networks generating hindlimb locomotion are located in the spinal cord. The mechanisms underlying spinal rhythmogenesis are unknown but network activity and interconnectivity of excitatory interneurons likely play prominent roles. Here, we investigate interconnectivity within the Shox2 inte...

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Main Authors: Ngoc T Ha, Kimberly J Dougherty
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2018-12-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/42519
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spelling doaj-3aaa98380d854b198104bc4f9a18f5b72021-05-05T16:23:35ZengeLife Sciences Publications LtdeLife2050-084X2018-12-01710.7554/eLife.42519Spinal Shox2 interneuron interconnectivity related to function and developmentNgoc T Ha0Kimberly J Dougherty1https://orcid.org/0000-0002-0807-574XDepartment of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, United StatesDepartment of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, United StatesNeuronal networks generating hindlimb locomotion are located in the spinal cord. The mechanisms underlying spinal rhythmogenesis are unknown but network activity and interconnectivity of excitatory interneurons likely play prominent roles. Here, we investigate interconnectivity within the Shox2 interneuron population, a subset of which has been suggested to be involved in locomotor rhythm generation, using paired recordings in isolated spinal cords or slices from transgenic mice. Sparse unidirectional connections consistent with chemical synaptic transmission and prominent bidirectional connections mediated by electrical synapses were present within distinct subsets of Shox2 interneurons. Moreover, bidirectional electrical connections were preferentially found between functionally-related Shox2 interneurons. Though prevalent in neonatal mice, electrical coupling began to decline in incidence and strength in mice ~ 3 weeks of age. Overall, our data suggest that gap junctional coupling promotes synchronization of Shox2 interneurons, and may be implicated in locomotor rhythmicity in developing mice.https://elifesciences.org/articles/42519spinal cordrhythm generationlocomotionsynaptic connectivitygap junctions
collection DOAJ
language English
format Article
sources DOAJ
author Ngoc T Ha
Kimberly J Dougherty
spellingShingle Ngoc T Ha
Kimberly J Dougherty
Spinal Shox2 interneuron interconnectivity related to function and development
eLife
spinal cord
rhythm generation
locomotion
synaptic connectivity
gap junctions
author_facet Ngoc T Ha
Kimberly J Dougherty
author_sort Ngoc T Ha
title Spinal Shox2 interneuron interconnectivity related to function and development
title_short Spinal Shox2 interneuron interconnectivity related to function and development
title_full Spinal Shox2 interneuron interconnectivity related to function and development
title_fullStr Spinal Shox2 interneuron interconnectivity related to function and development
title_full_unstemmed Spinal Shox2 interneuron interconnectivity related to function and development
title_sort spinal shox2 interneuron interconnectivity related to function and development
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2018-12-01
description Neuronal networks generating hindlimb locomotion are located in the spinal cord. The mechanisms underlying spinal rhythmogenesis are unknown but network activity and interconnectivity of excitatory interneurons likely play prominent roles. Here, we investigate interconnectivity within the Shox2 interneuron population, a subset of which has been suggested to be involved in locomotor rhythm generation, using paired recordings in isolated spinal cords or slices from transgenic mice. Sparse unidirectional connections consistent with chemical synaptic transmission and prominent bidirectional connections mediated by electrical synapses were present within distinct subsets of Shox2 interneurons. Moreover, bidirectional electrical connections were preferentially found between functionally-related Shox2 interneurons. Though prevalent in neonatal mice, electrical coupling began to decline in incidence and strength in mice ~ 3 weeks of age. Overall, our data suggest that gap junctional coupling promotes synchronization of Shox2 interneurons, and may be implicated in locomotor rhythmicity in developing mice.
topic spinal cord
rhythm generation
locomotion
synaptic connectivity
gap junctions
url https://elifesciences.org/articles/42519
work_keys_str_mv AT ngoctha spinalshox2interneuroninterconnectivityrelatedtofunctionanddevelopment
AT kimberlyjdougherty spinalshox2interneuroninterconnectivityrelatedtofunctionanddevelopment
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