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Hindbrain V2a Neurons Pattern Rhythmic Activity of Motor Neurons in a Reticulospinal Coculture

As the capacity to isolate distinct neuronal cell types has advanced over the past several decades, new two- and three-dimensional in vitro models of the interactions between different brain regions have expanded our understanding of human neurobiology and the origins of disease. These cultures deve...

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Autores principales: Bubnys, Adele, Kandel, Hagar, Kao, Lee Ming, Pfaff, Donald, Tabansky, Inna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6811747/
https://www.ncbi.nlm.nih.gov/pubmed/31680817
http://dx.doi.org/10.3389/fnins.2019.01077
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author Bubnys, Adele
Kandel, Hagar
Kao, Lee Ming
Pfaff, Donald
Tabansky, Inna
author_facet Bubnys, Adele
Kandel, Hagar
Kao, Lee Ming
Pfaff, Donald
Tabansky, Inna
author_sort Bubnys, Adele
collection PubMed
description As the capacity to isolate distinct neuronal cell types has advanced over the past several decades, new two- and three-dimensional in vitro models of the interactions between different brain regions have expanded our understanding of human neurobiology and the origins of disease. These cultures develop distinctive patterns of activity, but the extent that these patterns are determined by the molecular identity of individual cell types versus the specific pattern of network connectivity is unclear. To address the question of how individual cell types interact in vitro, we developed a simplified culture using two excitatory neuronal subtypes known to participate in the in vivo reticulospinal circuit: HB9(+) spinal motor neurons and Chx10(+) hindbrain V2a neurons. Here, we report the emergence of cell type-specific patterns of activity in culture; on their own, Chx10(+) neurons developed regular, synchronized bursts of activity that recruited neurons across the entire culture, whereas HB9(+) neuron activity consisted of an irregular pattern. When these two subtypes were cocultured, HB9(+) neurons developed synchronized network bursts that were precisely correlated with Chx10(+) neuron activity, thereby recreating an aspect of Chx10(+) neurons’ role in driving motor activity. These bursts were dependent on AMPA receptors. Our results demonstrate that the molecular classification of the neurons comprising in vitro networks is a crucial determinant of their activity. It is therefore possible to improve both the reproducibility and the applicability of in vitro neurobiological and disease models by carefully controlling the constituent mixtures of neuronal subtypes.
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spelling pubmed-68117472019-11-01 Hindbrain V2a Neurons Pattern Rhythmic Activity of Motor Neurons in a Reticulospinal Coculture Bubnys, Adele Kandel, Hagar Kao, Lee Ming Pfaff, Donald Tabansky, Inna Front Neurosci Neuroscience As the capacity to isolate distinct neuronal cell types has advanced over the past several decades, new two- and three-dimensional in vitro models of the interactions between different brain regions have expanded our understanding of human neurobiology and the origins of disease. These cultures develop distinctive patterns of activity, but the extent that these patterns are determined by the molecular identity of individual cell types versus the specific pattern of network connectivity is unclear. To address the question of how individual cell types interact in vitro, we developed a simplified culture using two excitatory neuronal subtypes known to participate in the in vivo reticulospinal circuit: HB9(+) spinal motor neurons and Chx10(+) hindbrain V2a neurons. Here, we report the emergence of cell type-specific patterns of activity in culture; on their own, Chx10(+) neurons developed regular, synchronized bursts of activity that recruited neurons across the entire culture, whereas HB9(+) neuron activity consisted of an irregular pattern. When these two subtypes were cocultured, HB9(+) neurons developed synchronized network bursts that were precisely correlated with Chx10(+) neuron activity, thereby recreating an aspect of Chx10(+) neurons’ role in driving motor activity. These bursts were dependent on AMPA receptors. Our results demonstrate that the molecular classification of the neurons comprising in vitro networks is a crucial determinant of their activity. It is therefore possible to improve both the reproducibility and the applicability of in vitro neurobiological and disease models by carefully controlling the constituent mixtures of neuronal subtypes. Frontiers Media S.A. 2019-10-17 /pmc/articles/PMC6811747/ /pubmed/31680817 http://dx.doi.org/10.3389/fnins.2019.01077 Text en Copyright © 2019 Bubnys, Kandel, Kao, Pfaff and Tabansky. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Bubnys, Adele
Kandel, Hagar
Kao, Lee Ming
Pfaff, Donald
Tabansky, Inna
Hindbrain V2a Neurons Pattern Rhythmic Activity of Motor Neurons in a Reticulospinal Coculture
title Hindbrain V2a Neurons Pattern Rhythmic Activity of Motor Neurons in a Reticulospinal Coculture
title_full Hindbrain V2a Neurons Pattern Rhythmic Activity of Motor Neurons in a Reticulospinal Coculture
title_fullStr Hindbrain V2a Neurons Pattern Rhythmic Activity of Motor Neurons in a Reticulospinal Coculture
title_full_unstemmed Hindbrain V2a Neurons Pattern Rhythmic Activity of Motor Neurons in a Reticulospinal Coculture
title_short Hindbrain V2a Neurons Pattern Rhythmic Activity of Motor Neurons in a Reticulospinal Coculture
title_sort hindbrain v2a neurons pattern rhythmic activity of motor neurons in a reticulospinal coculture
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6811747/
https://www.ncbi.nlm.nih.gov/pubmed/31680817
http://dx.doi.org/10.3389/fnins.2019.01077
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