Cargando…

Synergism of type 1 metabotropic and ionotropic glutamate receptors in cerebellar molecular layer interneurons in vivo

Type 1 metabotropic glutamate receptors (mGluR1s) are key elements in neuronal signaling. While their function is well documented in slices, requirements for their activation in vivo are poorly understood. We examine this question in adult mice in vivo using 2-photon imaging of cerebellar molecular...

Descripción completa

Detalles Bibliográficos
Autores principales: Bao, Jin, Graupner, Michael, Astorga, Guadalupe, Collin, Thibault, Jalil, Abdelali, Indriati, Dwi Wahyu, Bradley, Jonathan, Shigemoto, Ryuichi, Llano, Isabel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7220378/
https://www.ncbi.nlm.nih.gov/pubmed/32401196
http://dx.doi.org/10.7554/eLife.56839
_version_ 1783533147870199808
author Bao, Jin
Graupner, Michael
Astorga, Guadalupe
Collin, Thibault
Jalil, Abdelali
Indriati, Dwi Wahyu
Bradley, Jonathan
Shigemoto, Ryuichi
Llano, Isabel
author_facet Bao, Jin
Graupner, Michael
Astorga, Guadalupe
Collin, Thibault
Jalil, Abdelali
Indriati, Dwi Wahyu
Bradley, Jonathan
Shigemoto, Ryuichi
Llano, Isabel
author_sort Bao, Jin
collection PubMed
description Type 1 metabotropic glutamate receptors (mGluR1s) are key elements in neuronal signaling. While their function is well documented in slices, requirements for their activation in vivo are poorly understood. We examine this question in adult mice in vivo using 2-photon imaging of cerebellar molecular layer interneurons (MLIs) expressing GCaMP. In anesthetized mice, parallel fiber activation evokes beam-like Ca(i) rises in postsynaptic MLIs which depend on co-activation of mGluR1s and ionotropic glutamate receptors (iGluRs). In awake mice, blocking mGluR1 decreases Ca(i) rises associated with locomotion. In vitro studies and freeze-fracture electron microscopy show that the iGluR-mGluR1 interaction is synergistic and favored by close association of the two classes of receptors. Altogether our results suggest that mGluR1s, acting in synergy with iGluRs, potently contribute to processing cerebellar neuronal signaling under physiological conditions.
format Online
Article
Text
id pubmed-7220378
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-72203782020-05-15 Synergism of type 1 metabotropic and ionotropic glutamate receptors in cerebellar molecular layer interneurons in vivo Bao, Jin Graupner, Michael Astorga, Guadalupe Collin, Thibault Jalil, Abdelali Indriati, Dwi Wahyu Bradley, Jonathan Shigemoto, Ryuichi Llano, Isabel eLife Neuroscience Type 1 metabotropic glutamate receptors (mGluR1s) are key elements in neuronal signaling. While their function is well documented in slices, requirements for their activation in vivo are poorly understood. We examine this question in adult mice in vivo using 2-photon imaging of cerebellar molecular layer interneurons (MLIs) expressing GCaMP. In anesthetized mice, parallel fiber activation evokes beam-like Ca(i) rises in postsynaptic MLIs which depend on co-activation of mGluR1s and ionotropic glutamate receptors (iGluRs). In awake mice, blocking mGluR1 decreases Ca(i) rises associated with locomotion. In vitro studies and freeze-fracture electron microscopy show that the iGluR-mGluR1 interaction is synergistic and favored by close association of the two classes of receptors. Altogether our results suggest that mGluR1s, acting in synergy with iGluRs, potently contribute to processing cerebellar neuronal signaling under physiological conditions. eLife Sciences Publications, Ltd 2020-05-13 /pmc/articles/PMC7220378/ /pubmed/32401196 http://dx.doi.org/10.7554/eLife.56839 Text en © 2020, Bao et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Bao, Jin
Graupner, Michael
Astorga, Guadalupe
Collin, Thibault
Jalil, Abdelali
Indriati, Dwi Wahyu
Bradley, Jonathan
Shigemoto, Ryuichi
Llano, Isabel
Synergism of type 1 metabotropic and ionotropic glutamate receptors in cerebellar molecular layer interneurons in vivo
title Synergism of type 1 metabotropic and ionotropic glutamate receptors in cerebellar molecular layer interneurons in vivo
title_full Synergism of type 1 metabotropic and ionotropic glutamate receptors in cerebellar molecular layer interneurons in vivo
title_fullStr Synergism of type 1 metabotropic and ionotropic glutamate receptors in cerebellar molecular layer interneurons in vivo
title_full_unstemmed Synergism of type 1 metabotropic and ionotropic glutamate receptors in cerebellar molecular layer interneurons in vivo
title_short Synergism of type 1 metabotropic and ionotropic glutamate receptors in cerebellar molecular layer interneurons in vivo
title_sort synergism of type 1 metabotropic and ionotropic glutamate receptors in cerebellar molecular layer interneurons in vivo
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7220378/
https://www.ncbi.nlm.nih.gov/pubmed/32401196
http://dx.doi.org/10.7554/eLife.56839
work_keys_str_mv AT baojin synergismoftype1metabotropicandionotropicglutamatereceptorsincerebellarmolecularlayerinterneuronsinvivo
AT graupnermichael synergismoftype1metabotropicandionotropicglutamatereceptorsincerebellarmolecularlayerinterneuronsinvivo
AT astorgaguadalupe synergismoftype1metabotropicandionotropicglutamatereceptorsincerebellarmolecularlayerinterneuronsinvivo
AT collinthibault synergismoftype1metabotropicandionotropicglutamatereceptorsincerebellarmolecularlayerinterneuronsinvivo
AT jalilabdelali synergismoftype1metabotropicandionotropicglutamatereceptorsincerebellarmolecularlayerinterneuronsinvivo
AT indriatidwiwahyu synergismoftype1metabotropicandionotropicglutamatereceptorsincerebellarmolecularlayerinterneuronsinvivo
AT bradleyjonathan synergismoftype1metabotropicandionotropicglutamatereceptorsincerebellarmolecularlayerinterneuronsinvivo
AT shigemotoryuichi synergismoftype1metabotropicandionotropicglutamatereceptorsincerebellarmolecularlayerinterneuronsinvivo
AT llanoisabel synergismoftype1metabotropicandionotropicglutamatereceptorsincerebellarmolecularlayerinterneuronsinvivo