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Optogenetic activation of mGluR1 signaling in the cerebellum induces synaptic plasticity
Neuronal plasticity underlying cerebellar learning behavior is strongly associated with type 1 metabotropic glutamate receptor (mGluR1) signaling. Activation of mGluR1 leads to activation of the G(q/11) pathway, which is involved in inducing synaptic plasticity at the parallel fiber-Purkinje cell sy...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826949/ https://www.ncbi.nlm.nih.gov/pubmed/36632066 http://dx.doi.org/10.1016/j.isci.2022.105828 |
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author | Surdin, Tatjana Preissing, Bianca Rohr, Lennard Grömmke, Michelle Böke, Hanna Barcik, Maike Azimi, Zohre Jancke, Dirk Herlitze, Stefan Mark, Melanie D. Siveke, Ida |
author_facet | Surdin, Tatjana Preissing, Bianca Rohr, Lennard Grömmke, Michelle Böke, Hanna Barcik, Maike Azimi, Zohre Jancke, Dirk Herlitze, Stefan Mark, Melanie D. Siveke, Ida |
author_sort | Surdin, Tatjana |
collection | PubMed |
description | Neuronal plasticity underlying cerebellar learning behavior is strongly associated with type 1 metabotropic glutamate receptor (mGluR1) signaling. Activation of mGluR1 leads to activation of the G(q/11) pathway, which is involved in inducing synaptic plasticity at the parallel fiber-Purkinje cell synapse (PF-PC) in form of long-term depression (LTD). To optogenetically modulate mGluR1 signaling we fused mouse melanopsin (OPN4) that activates the G(q/11) pathway to the C-termini of mGluR1 splice variants (OPN4-mGluR1a and OPN4-mGluR1b). Activation of both OPN4-mGluR1 variants showed robust Ca(2+) increase in HEK cells and PCs of cerebellar slices. We provide the prove-of-concept approach to modulate synaptic plasticity via optogenetic activation of OPN4-mGluR1a inducing LTD at the PF-PC synapse in vitro. Moreover, we demonstrate that light activation of mGluR1a signaling pathway by OPN4-mGluR1a in PCs leads to an increase in intrinsic activity of PCs in vivo and improved cerebellum driven learning behavior. |
format | Online Article Text |
id | pubmed-9826949 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-98269492023-01-10 Optogenetic activation of mGluR1 signaling in the cerebellum induces synaptic plasticity Surdin, Tatjana Preissing, Bianca Rohr, Lennard Grömmke, Michelle Böke, Hanna Barcik, Maike Azimi, Zohre Jancke, Dirk Herlitze, Stefan Mark, Melanie D. Siveke, Ida iScience Article Neuronal plasticity underlying cerebellar learning behavior is strongly associated with type 1 metabotropic glutamate receptor (mGluR1) signaling. Activation of mGluR1 leads to activation of the G(q/11) pathway, which is involved in inducing synaptic plasticity at the parallel fiber-Purkinje cell synapse (PF-PC) in form of long-term depression (LTD). To optogenetically modulate mGluR1 signaling we fused mouse melanopsin (OPN4) that activates the G(q/11) pathway to the C-termini of mGluR1 splice variants (OPN4-mGluR1a and OPN4-mGluR1b). Activation of both OPN4-mGluR1 variants showed robust Ca(2+) increase in HEK cells and PCs of cerebellar slices. We provide the prove-of-concept approach to modulate synaptic plasticity via optogenetic activation of OPN4-mGluR1a inducing LTD at the PF-PC synapse in vitro. Moreover, we demonstrate that light activation of mGluR1a signaling pathway by OPN4-mGluR1a in PCs leads to an increase in intrinsic activity of PCs in vivo and improved cerebellum driven learning behavior. Elsevier 2022-12-17 /pmc/articles/PMC9826949/ /pubmed/36632066 http://dx.doi.org/10.1016/j.isci.2022.105828 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Surdin, Tatjana Preissing, Bianca Rohr, Lennard Grömmke, Michelle Böke, Hanna Barcik, Maike Azimi, Zohre Jancke, Dirk Herlitze, Stefan Mark, Melanie D. Siveke, Ida Optogenetic activation of mGluR1 signaling in the cerebellum induces synaptic plasticity |
title | Optogenetic activation of mGluR1 signaling in the cerebellum induces synaptic plasticity |
title_full | Optogenetic activation of mGluR1 signaling in the cerebellum induces synaptic plasticity |
title_fullStr | Optogenetic activation of mGluR1 signaling in the cerebellum induces synaptic plasticity |
title_full_unstemmed | Optogenetic activation of mGluR1 signaling in the cerebellum induces synaptic plasticity |
title_short | Optogenetic activation of mGluR1 signaling in the cerebellum induces synaptic plasticity |
title_sort | optogenetic activation of mglur1 signaling in the cerebellum induces synaptic plasticity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826949/ https://www.ncbi.nlm.nih.gov/pubmed/36632066 http://dx.doi.org/10.1016/j.isci.2022.105828 |
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