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Locomotion dependent neuron-glia interactions control neurogenesis and regeneration in the adult zebrafish spinal cord
Physical exercise stimulates adult neurogenesis, yet the underlying mechanisms remain poorly understood. A fundamental component of the innate neuroregenerative capacity of zebrafish is the proliferative and neurogenic ability of the neural stem/progenitor cells. Here, we show that in the intact spi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8357999/ https://www.ncbi.nlm.nih.gov/pubmed/34381039 http://dx.doi.org/10.1038/s41467-021-25052-1 |
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author | Chang, Weipang Pedroni, Andrea Bertuzzi, Maria Kizil, Caghan Simon, András Ampatzis, Konstantinos |
author_facet | Chang, Weipang Pedroni, Andrea Bertuzzi, Maria Kizil, Caghan Simon, András Ampatzis, Konstantinos |
author_sort | Chang, Weipang |
collection | PubMed |
description | Physical exercise stimulates adult neurogenesis, yet the underlying mechanisms remain poorly understood. A fundamental component of the innate neuroregenerative capacity of zebrafish is the proliferative and neurogenic ability of the neural stem/progenitor cells. Here, we show that in the intact spinal cord, this plasticity response can be activated by physical exercise by demonstrating that the cholinergic neurotransmission from spinal locomotor neurons activates spinal neural stem/progenitor cells, leading to neurogenesis in the adult zebrafish. We also show that GABA acts in a non-synaptic fashion to maintain neural stem/progenitor cell quiescence in the spinal cord and that training-induced activation of neurogenesis requires a reduction of GABA(A) receptors. Furthermore, both pharmacological stimulation of cholinergic receptors, as well as interference with GABAergic signaling, promote functional recovery after spinal cord injury. Our findings provide a model for locomotor networks’ activity-dependent neurogenesis during homeostasis and regeneration in the adult zebrafish spinal cord. |
format | Online Article Text |
id | pubmed-8357999 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83579992021-08-30 Locomotion dependent neuron-glia interactions control neurogenesis and regeneration in the adult zebrafish spinal cord Chang, Weipang Pedroni, Andrea Bertuzzi, Maria Kizil, Caghan Simon, András Ampatzis, Konstantinos Nat Commun Article Physical exercise stimulates adult neurogenesis, yet the underlying mechanisms remain poorly understood. A fundamental component of the innate neuroregenerative capacity of zebrafish is the proliferative and neurogenic ability of the neural stem/progenitor cells. Here, we show that in the intact spinal cord, this plasticity response can be activated by physical exercise by demonstrating that the cholinergic neurotransmission from spinal locomotor neurons activates spinal neural stem/progenitor cells, leading to neurogenesis in the adult zebrafish. We also show that GABA acts in a non-synaptic fashion to maintain neural stem/progenitor cell quiescence in the spinal cord and that training-induced activation of neurogenesis requires a reduction of GABA(A) receptors. Furthermore, both pharmacological stimulation of cholinergic receptors, as well as interference with GABAergic signaling, promote functional recovery after spinal cord injury. Our findings provide a model for locomotor networks’ activity-dependent neurogenesis during homeostasis and regeneration in the adult zebrafish spinal cord. Nature Publishing Group UK 2021-08-11 /pmc/articles/PMC8357999/ /pubmed/34381039 http://dx.doi.org/10.1038/s41467-021-25052-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Chang, Weipang Pedroni, Andrea Bertuzzi, Maria Kizil, Caghan Simon, András Ampatzis, Konstantinos Locomotion dependent neuron-glia interactions control neurogenesis and regeneration in the adult zebrafish spinal cord |
title | Locomotion dependent neuron-glia interactions control neurogenesis and regeneration in the adult zebrafish spinal cord |
title_full | Locomotion dependent neuron-glia interactions control neurogenesis and regeneration in the adult zebrafish spinal cord |
title_fullStr | Locomotion dependent neuron-glia interactions control neurogenesis and regeneration in the adult zebrafish spinal cord |
title_full_unstemmed | Locomotion dependent neuron-glia interactions control neurogenesis and regeneration in the adult zebrafish spinal cord |
title_short | Locomotion dependent neuron-glia interactions control neurogenesis and regeneration in the adult zebrafish spinal cord |
title_sort | locomotion dependent neuron-glia interactions control neurogenesis and regeneration in the adult zebrafish spinal cord |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8357999/ https://www.ncbi.nlm.nih.gov/pubmed/34381039 http://dx.doi.org/10.1038/s41467-021-25052-1 |
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