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Pitx2 cholinergic interneurons are the source of C bouton synapses on brainstem motor neurons

Cholinergic neuromodulation has been described throughout the brain and has been implicated in various functions including attention, food intake and response to stress. Cholinergic modulation is also thought to be important for regulating motor systems, as revealed by studies of large cholinergic s...

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Autores principales: Rozani, Ismini, Tsapara, Georgia, Witts, Emily C., Deaville, S. James, Miles, Gareth B., Zagoraiou, Laskaro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6426951/
https://www.ncbi.nlm.nih.gov/pubmed/30894556
http://dx.doi.org/10.1038/s41598-019-39996-4
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author Rozani, Ismini
Tsapara, Georgia
Witts, Emily C.
Deaville, S. James
Miles, Gareth B.
Zagoraiou, Laskaro
author_facet Rozani, Ismini
Tsapara, Georgia
Witts, Emily C.
Deaville, S. James
Miles, Gareth B.
Zagoraiou, Laskaro
author_sort Rozani, Ismini
collection PubMed
description Cholinergic neuromodulation has been described throughout the brain and has been implicated in various functions including attention, food intake and response to stress. Cholinergic modulation is also thought to be important for regulating motor systems, as revealed by studies of large cholinergic synapses on spinal motor neurons, called C boutons, which seem to control motor neuron excitability in a task-dependent manner. C boutons on spinal motor neurons stem from spinal interneurons that express the transcription factor Pitx2. C boutons have also been identified on the motor neurons of specific cranial nuclei. However, the source and roles of cranial C boutons are less clear. Previous studies suggest that they originate from Pitx2+ and Pitx2− neurons, in contrast to spinal cord C boutons that originate solely from Pitx2 neurons. Here, we address this controversy using mouse genetics, and demonstrate that brainstem C boutons are Pitx2+ derived. We also identify new Pitx2 populations and map the cholinergic Pitx2 neurons of the mouse brain. Taken together, our data present important new information about the anatomical organization of cholinergic systems which impact motor systems of the brainstem. These findings will enable further analyses of the specific roles of cholinergic modulation in motor control.
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spelling pubmed-64269512019-03-28 Pitx2 cholinergic interneurons are the source of C bouton synapses on brainstem motor neurons Rozani, Ismini Tsapara, Georgia Witts, Emily C. Deaville, S. James Miles, Gareth B. Zagoraiou, Laskaro Sci Rep Article Cholinergic neuromodulation has been described throughout the brain and has been implicated in various functions including attention, food intake and response to stress. Cholinergic modulation is also thought to be important for regulating motor systems, as revealed by studies of large cholinergic synapses on spinal motor neurons, called C boutons, which seem to control motor neuron excitability in a task-dependent manner. C boutons on spinal motor neurons stem from spinal interneurons that express the transcription factor Pitx2. C boutons have also been identified on the motor neurons of specific cranial nuclei. However, the source and roles of cranial C boutons are less clear. Previous studies suggest that they originate from Pitx2+ and Pitx2− neurons, in contrast to spinal cord C boutons that originate solely from Pitx2 neurons. Here, we address this controversy using mouse genetics, and demonstrate that brainstem C boutons are Pitx2+ derived. We also identify new Pitx2 populations and map the cholinergic Pitx2 neurons of the mouse brain. Taken together, our data present important new information about the anatomical organization of cholinergic systems which impact motor systems of the brainstem. These findings will enable further analyses of the specific roles of cholinergic modulation in motor control. Nature Publishing Group UK 2019-03-20 /pmc/articles/PMC6426951/ /pubmed/30894556 http://dx.doi.org/10.1038/s41598-019-39996-4 Text en © The Author(s) 2019 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
Rozani, Ismini
Tsapara, Georgia
Witts, Emily C.
Deaville, S. James
Miles, Gareth B.
Zagoraiou, Laskaro
Pitx2 cholinergic interneurons are the source of C bouton synapses on brainstem motor neurons
title Pitx2 cholinergic interneurons are the source of C bouton synapses on brainstem motor neurons
title_full Pitx2 cholinergic interneurons are the source of C bouton synapses on brainstem motor neurons
title_fullStr Pitx2 cholinergic interneurons are the source of C bouton synapses on brainstem motor neurons
title_full_unstemmed Pitx2 cholinergic interneurons are the source of C bouton synapses on brainstem motor neurons
title_short Pitx2 cholinergic interneurons are the source of C bouton synapses on brainstem motor neurons
title_sort pitx2 cholinergic interneurons are the source of c bouton synapses on brainstem motor neurons
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6426951/
https://www.ncbi.nlm.nih.gov/pubmed/30894556
http://dx.doi.org/10.1038/s41598-019-39996-4
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