The Temporal Mechanisms Guiding Interneuron Differentiation in the Spinal Cord

Neurogenesis timing is an essential developmental mechanism for neuronal diversity and organization throughout the central nervous system. In the mouse spinal cord, growing evidence is beginning to reveal that neurogenesis timing acts in tandem with spatial molecular controls to diversify molecularl...

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Main Authors: Dylan Deska-Gauthier, Ying Zhang
Format: Article
Language:English
Published: MDPI AG 2021-07-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/22/15/8025
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spelling doaj-d3aebfafa79a48539e4b4badb4588c092021-08-06T15:25:09ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672021-07-01228025802510.3390/ijms22158025The Temporal Mechanisms Guiding Interneuron Differentiation in the Spinal CordDylan Deska-Gauthier0Ying Zhang1Brain Repair Center, Department of Neuroscience, Faculty of Medicine, Dalhousie University, Halifax, NS B3H 4R2, CanadaBrain Repair Center, Department of Neuroscience, Faculty of Medicine, Dalhousie University, Halifax, NS B3H 4R2, CanadaNeurogenesis timing is an essential developmental mechanism for neuronal diversity and organization throughout the central nervous system. In the mouse spinal cord, growing evidence is beginning to reveal that neurogenesis timing acts in tandem with spatial molecular controls to diversify molecularly and functionally distinct post-mitotic interneuron subpopulations. Particularly, in some cases, this temporal ordering of interneuron differentiation has been shown to instruct specific sensorimotor circuit wirings. In zebrafish, in vivo preparations have revealed that sequential neurogenesis waves of interneurons and motor neurons form speed-dependent locomotor circuits throughout the spinal cord and brainstem. In the present review, we discuss temporal principals of interneuron diversity taken from both mouse and zebrafish systems highlighting how each can lend illuminating insights to the other. Moving forward, it is important to combine the collective knowledge from different systems to eventually understand how temporally regulated subpopulation function differentially across speed- and/or state-dependent sensorimotor movement tasks.https://www.mdpi.com/1422-0067/22/15/8025spinal cordinterneuronsubpopulationsneurogenesismousezebra fish
collection DOAJ
language English
format Article
sources DOAJ
author Dylan Deska-Gauthier
Ying Zhang
spellingShingle Dylan Deska-Gauthier
Ying Zhang
The Temporal Mechanisms Guiding Interneuron Differentiation in the Spinal Cord
International Journal of Molecular Sciences
spinal cord
interneuron
subpopulations
neurogenesis
mouse
zebra fish
author_facet Dylan Deska-Gauthier
Ying Zhang
author_sort Dylan Deska-Gauthier
title The Temporal Mechanisms Guiding Interneuron Differentiation in the Spinal Cord
title_short The Temporal Mechanisms Guiding Interneuron Differentiation in the Spinal Cord
title_full The Temporal Mechanisms Guiding Interneuron Differentiation in the Spinal Cord
title_fullStr The Temporal Mechanisms Guiding Interneuron Differentiation in the Spinal Cord
title_full_unstemmed The Temporal Mechanisms Guiding Interneuron Differentiation in the Spinal Cord
title_sort temporal mechanisms guiding interneuron differentiation in the spinal cord
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1661-6596
1422-0067
publishDate 2021-07-01
description Neurogenesis timing is an essential developmental mechanism for neuronal diversity and organization throughout the central nervous system. In the mouse spinal cord, growing evidence is beginning to reveal that neurogenesis timing acts in tandem with spatial molecular controls to diversify molecularly and functionally distinct post-mitotic interneuron subpopulations. Particularly, in some cases, this temporal ordering of interneuron differentiation has been shown to instruct specific sensorimotor circuit wirings. In zebrafish, in vivo preparations have revealed that sequential neurogenesis waves of interneurons and motor neurons form speed-dependent locomotor circuits throughout the spinal cord and brainstem. In the present review, we discuss temporal principals of interneuron diversity taken from both mouse and zebrafish systems highlighting how each can lend illuminating insights to the other. Moving forward, it is important to combine the collective knowledge from different systems to eventually understand how temporally regulated subpopulation function differentially across speed- and/or state-dependent sensorimotor movement tasks.
topic spinal cord
interneuron
subpopulations
neurogenesis
mouse
zebra fish
url https://www.mdpi.com/1422-0067/22/15/8025
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