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mGlu1 Receptors Monopolize the Synaptic Control of Cerebellar Purkinje Cells by Epigenetically Down-Regulating mGlu5 Receptors
In cerebellar Purkinje cells (PCs) type-1 metabotropic glutamate (mGlu1) receptors play a key role in motor learning and drive the refinement of synaptic innervation during postnatal development. The cognate mGlu5 receptor is absent in mature PCs and shows low expression levels in the adult cerebell...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6127335/ https://www.ncbi.nlm.nih.gov/pubmed/30190524 http://dx.doi.org/10.1038/s41598-018-31369-7 |
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author | Notartomaso, Serena Nakao, Harumi Mascio, Giada Scarselli, Pamela Cannella, Milena Zappulla, Cristina Madonna, Michele Motolese, Marta Gradini, Roberto Liberatore, Francesca Zonta, Micaela Carmignoto, Giorgio Battaglia, Giuseppe Bruno, Valeria Watanabe, Masahiko Aiba, Atsu Nicoletti, Ferdinando |
author_facet | Notartomaso, Serena Nakao, Harumi Mascio, Giada Scarselli, Pamela Cannella, Milena Zappulla, Cristina Madonna, Michele Motolese, Marta Gradini, Roberto Liberatore, Francesca Zonta, Micaela Carmignoto, Giorgio Battaglia, Giuseppe Bruno, Valeria Watanabe, Masahiko Aiba, Atsu Nicoletti, Ferdinando |
author_sort | Notartomaso, Serena |
collection | PubMed |
description | In cerebellar Purkinje cells (PCs) type-1 metabotropic glutamate (mGlu1) receptors play a key role in motor learning and drive the refinement of synaptic innervation during postnatal development. The cognate mGlu5 receptor is absent in mature PCs and shows low expression levels in the adult cerebellar cortex. Here we found that mGlu5 receptors were heavily expressed by PCs in the early postnatal life, when mGlu1α receptors were barely detectable. The developmental decline of mGlu5 receptors coincided with the appearance of mGlu1α receptors in PCs, and both processes were associated with specular changes in CpG methylation in the corresponding gene promoters. It was the mGlu1 receptor that drove the elimination of mGlu5 receptors from PCs, as shown by data obtained with conditional mGlu1α receptor knockout mice and with targeted pharmacological treatments during critical developmental time windows. The suppressing activity of mGlu1 receptors on mGlu5 receptor was maintained in mature PCs, suggesting that expression of mGlu1α and mGlu5 receptors is mutually exclusive in PCs. These findings add complexity to the the finely tuned mechanisms that regulate PC biology during development and in the adult life and lay the groundwork for an in-depth analysis of the role played by mGlu5 receptors in PC maturation. |
format | Online Article Text |
id | pubmed-6127335 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61273352018-09-10 mGlu1 Receptors Monopolize the Synaptic Control of Cerebellar Purkinje Cells by Epigenetically Down-Regulating mGlu5 Receptors Notartomaso, Serena Nakao, Harumi Mascio, Giada Scarselli, Pamela Cannella, Milena Zappulla, Cristina Madonna, Michele Motolese, Marta Gradini, Roberto Liberatore, Francesca Zonta, Micaela Carmignoto, Giorgio Battaglia, Giuseppe Bruno, Valeria Watanabe, Masahiko Aiba, Atsu Nicoletti, Ferdinando Sci Rep Article In cerebellar Purkinje cells (PCs) type-1 metabotropic glutamate (mGlu1) receptors play a key role in motor learning and drive the refinement of synaptic innervation during postnatal development. The cognate mGlu5 receptor is absent in mature PCs and shows low expression levels in the adult cerebellar cortex. Here we found that mGlu5 receptors were heavily expressed by PCs in the early postnatal life, when mGlu1α receptors were barely detectable. The developmental decline of mGlu5 receptors coincided with the appearance of mGlu1α receptors in PCs, and both processes were associated with specular changes in CpG methylation in the corresponding gene promoters. It was the mGlu1 receptor that drove the elimination of mGlu5 receptors from PCs, as shown by data obtained with conditional mGlu1α receptor knockout mice and with targeted pharmacological treatments during critical developmental time windows. The suppressing activity of mGlu1 receptors on mGlu5 receptor was maintained in mature PCs, suggesting that expression of mGlu1α and mGlu5 receptors is mutually exclusive in PCs. These findings add complexity to the the finely tuned mechanisms that regulate PC biology during development and in the adult life and lay the groundwork for an in-depth analysis of the role played by mGlu5 receptors in PC maturation. Nature Publishing Group UK 2018-09-06 /pmc/articles/PMC6127335/ /pubmed/30190524 http://dx.doi.org/10.1038/s41598-018-31369-7 Text en © The Author(s) 2018 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 Notartomaso, Serena Nakao, Harumi Mascio, Giada Scarselli, Pamela Cannella, Milena Zappulla, Cristina Madonna, Michele Motolese, Marta Gradini, Roberto Liberatore, Francesca Zonta, Micaela Carmignoto, Giorgio Battaglia, Giuseppe Bruno, Valeria Watanabe, Masahiko Aiba, Atsu Nicoletti, Ferdinando mGlu1 Receptors Monopolize the Synaptic Control of Cerebellar Purkinje Cells by Epigenetically Down-Regulating mGlu5 Receptors |
title | mGlu1 Receptors Monopolize the Synaptic Control of Cerebellar Purkinje Cells by Epigenetically Down-Regulating mGlu5 Receptors |
title_full | mGlu1 Receptors Monopolize the Synaptic Control of Cerebellar Purkinje Cells by Epigenetically Down-Regulating mGlu5 Receptors |
title_fullStr | mGlu1 Receptors Monopolize the Synaptic Control of Cerebellar Purkinje Cells by Epigenetically Down-Regulating mGlu5 Receptors |
title_full_unstemmed | mGlu1 Receptors Monopolize the Synaptic Control of Cerebellar Purkinje Cells by Epigenetically Down-Regulating mGlu5 Receptors |
title_short | mGlu1 Receptors Monopolize the Synaptic Control of Cerebellar Purkinje Cells by Epigenetically Down-Regulating mGlu5 Receptors |
title_sort | mglu1 receptors monopolize the synaptic control of cerebellar purkinje cells by epigenetically down-regulating mglu5 receptors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6127335/ https://www.ncbi.nlm.nih.gov/pubmed/30190524 http://dx.doi.org/10.1038/s41598-018-31369-7 |
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