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Segregation of glutamatergic and cholinergic transmission at the mixed motoneuron Renshaw cell synapse
In neonatal mice motoneurons excite Renshaw cells by releasing both acetylcholine (ACh) and glutamate. These two neurotransmitters activate two types of nicotinic receptors (nAChRs) (the homomeric α(7) receptors and the heteromeric α*ß* receptors) as well as the two types of glutamate receptors (Gl...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5481398/ https://www.ncbi.nlm.nih.gov/pubmed/28642492 http://dx.doi.org/10.1038/s41598-017-04266-8 |
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author | Lamotte d’Incamps, Boris Bhumbra, Gardave S. Foster, Joshua D. Beato, Marco Ascher, Philippe |
author_facet | Lamotte d’Incamps, Boris Bhumbra, Gardave S. Foster, Joshua D. Beato, Marco Ascher, Philippe |
author_sort | Lamotte d’Incamps, Boris |
collection | PubMed |
description | In neonatal mice motoneurons excite Renshaw cells by releasing both acetylcholine (ACh) and glutamate. These two neurotransmitters activate two types of nicotinic receptors (nAChRs) (the homomeric α(7) receptors and the heteromeric α*ß* receptors) as well as the two types of glutamate receptors (GluRs) (AMPARs and NMDARs). Using paired recordings, we confirm that a single motoneuron can release both transmitters on a single post-synaptic Renshaw cell. We then show that co-transmission is preserved in adult animals. Kinetic analysis of miniature EPSCs revealed quantal release of mixed events associating AMPARs and NMDARs, as well as α(7) and α*ß* nAChRs, but no evidence was found for mEPSCs associating nAChRs with GluRs. Bayesian Quantal Analysis (BQA) of evoked EPSCs showed that the number of functional contacts on a single Renshaw cell is more than halved when the nicotinic receptors are blocked, confirming that the two neurotransmitters systems are segregated. Our observations can be explained if ACh and glutamate are released from common vesicles onto spatially segregated post-synaptic receptors clusters, but a pre-synaptic segregation of cholinergic and glutamatergic release sites is also possible. |
format | Online Article Text |
id | pubmed-5481398 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54813982017-06-26 Segregation of glutamatergic and cholinergic transmission at the mixed motoneuron Renshaw cell synapse Lamotte d’Incamps, Boris Bhumbra, Gardave S. Foster, Joshua D. Beato, Marco Ascher, Philippe Sci Rep Article In neonatal mice motoneurons excite Renshaw cells by releasing both acetylcholine (ACh) and glutamate. These two neurotransmitters activate two types of nicotinic receptors (nAChRs) (the homomeric α(7) receptors and the heteromeric α*ß* receptors) as well as the two types of glutamate receptors (GluRs) (AMPARs and NMDARs). Using paired recordings, we confirm that a single motoneuron can release both transmitters on a single post-synaptic Renshaw cell. We then show that co-transmission is preserved in adult animals. Kinetic analysis of miniature EPSCs revealed quantal release of mixed events associating AMPARs and NMDARs, as well as α(7) and α*ß* nAChRs, but no evidence was found for mEPSCs associating nAChRs with GluRs. Bayesian Quantal Analysis (BQA) of evoked EPSCs showed that the number of functional contacts on a single Renshaw cell is more than halved when the nicotinic receptors are blocked, confirming that the two neurotransmitters systems are segregated. Our observations can be explained if ACh and glutamate are released from common vesicles onto spatially segregated post-synaptic receptors clusters, but a pre-synaptic segregation of cholinergic and glutamatergic release sites is also possible. Nature Publishing Group UK 2017-06-22 /pmc/articles/PMC5481398/ /pubmed/28642492 http://dx.doi.org/10.1038/s41598-017-04266-8 Text en © The Author(s) 2017 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/. |
spellingShingle | Article Lamotte d’Incamps, Boris Bhumbra, Gardave S. Foster, Joshua D. Beato, Marco Ascher, Philippe Segregation of glutamatergic and cholinergic transmission at the mixed motoneuron Renshaw cell synapse |
title | Segregation of glutamatergic and cholinergic transmission at the mixed motoneuron Renshaw cell synapse |
title_full | Segregation of glutamatergic and cholinergic transmission at the mixed motoneuron Renshaw cell synapse |
title_fullStr | Segregation of glutamatergic and cholinergic transmission at the mixed motoneuron Renshaw cell synapse |
title_full_unstemmed | Segregation of glutamatergic and cholinergic transmission at the mixed motoneuron Renshaw cell synapse |
title_short | Segregation of glutamatergic and cholinergic transmission at the mixed motoneuron Renshaw cell synapse |
title_sort | segregation of glutamatergic and cholinergic transmission at the mixed motoneuron renshaw cell synapse |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5481398/ https://www.ncbi.nlm.nih.gov/pubmed/28642492 http://dx.doi.org/10.1038/s41598-017-04266-8 |
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