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Causal Interrogation of Neuronal Networks and Behavior through Virally Transduced Ivermectin Receptors

The causal interrogation of neuronal networks involved in specific behaviors requires the spatially and temporally controlled modulation of neuronal activity. For long-term manipulation of neuronal activity, chemogenetic tools provide a reasonable alternative to short-term optogenetic approaches. He...

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Autores principales: Obenhaus, Horst A., Rozov, Andrei, Bertocchi, Ilaria, Tang, Wannan, Kirsch, Joachim, Betz, Heinrich, Sprengel, Rolf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5004486/
https://www.ncbi.nlm.nih.gov/pubmed/27625595
http://dx.doi.org/10.3389/fnmol.2016.00075
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author Obenhaus, Horst A.
Rozov, Andrei
Bertocchi, Ilaria
Tang, Wannan
Kirsch, Joachim
Betz, Heinrich
Sprengel, Rolf
author_facet Obenhaus, Horst A.
Rozov, Andrei
Bertocchi, Ilaria
Tang, Wannan
Kirsch, Joachim
Betz, Heinrich
Sprengel, Rolf
author_sort Obenhaus, Horst A.
collection PubMed
description The causal interrogation of neuronal networks involved in specific behaviors requires the spatially and temporally controlled modulation of neuronal activity. For long-term manipulation of neuronal activity, chemogenetic tools provide a reasonable alternative to short-term optogenetic approaches. Here we show that virus mediated gene transfer of the ivermectin (IVM) activated glycine receptor mutant GlyRα(1)(AG) can be used for the selective and reversible silencing of specific neuronal networks in mice. In the striatum, dorsal hippocampus, and olfactory bulb, GlyRα(1)(AG) promoted IVM dependent effects in representative behavioral assays. Moreover, GlyRα(1)(AG) mediated silencing had a strong and reversible impact on neuronal ensemble activity and c-Fos activation in the olfactory bulb. Together our results demonstrate that long-term, reversible and re-inducible neuronal silencing via GlyRα(1)(AG) is a promising tool for the interrogation of network mechanisms underlying the control of behavior and memory formation.
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spelling pubmed-50044862016-09-13 Causal Interrogation of Neuronal Networks and Behavior through Virally Transduced Ivermectin Receptors Obenhaus, Horst A. Rozov, Andrei Bertocchi, Ilaria Tang, Wannan Kirsch, Joachim Betz, Heinrich Sprengel, Rolf Front Mol Neurosci Neuroscience The causal interrogation of neuronal networks involved in specific behaviors requires the spatially and temporally controlled modulation of neuronal activity. For long-term manipulation of neuronal activity, chemogenetic tools provide a reasonable alternative to short-term optogenetic approaches. Here we show that virus mediated gene transfer of the ivermectin (IVM) activated glycine receptor mutant GlyRα(1)(AG) can be used for the selective and reversible silencing of specific neuronal networks in mice. In the striatum, dorsal hippocampus, and olfactory bulb, GlyRα(1)(AG) promoted IVM dependent effects in representative behavioral assays. Moreover, GlyRα(1)(AG) mediated silencing had a strong and reversible impact on neuronal ensemble activity and c-Fos activation in the olfactory bulb. Together our results demonstrate that long-term, reversible and re-inducible neuronal silencing via GlyRα(1)(AG) is a promising tool for the interrogation of network mechanisms underlying the control of behavior and memory formation. Frontiers Media S.A. 2016-08-30 /pmc/articles/PMC5004486/ /pubmed/27625595 http://dx.doi.org/10.3389/fnmol.2016.00075 Text en Copyright © 2016 Obenhaus, Rozov, Bertocchi, Tang, Kirsch, Betz and Sprengel. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Obenhaus, Horst A.
Rozov, Andrei
Bertocchi, Ilaria
Tang, Wannan
Kirsch, Joachim
Betz, Heinrich
Sprengel, Rolf
Causal Interrogation of Neuronal Networks and Behavior through Virally Transduced Ivermectin Receptors
title Causal Interrogation of Neuronal Networks and Behavior through Virally Transduced Ivermectin Receptors
title_full Causal Interrogation of Neuronal Networks and Behavior through Virally Transduced Ivermectin Receptors
title_fullStr Causal Interrogation of Neuronal Networks and Behavior through Virally Transduced Ivermectin Receptors
title_full_unstemmed Causal Interrogation of Neuronal Networks and Behavior through Virally Transduced Ivermectin Receptors
title_short Causal Interrogation of Neuronal Networks and Behavior through Virally Transduced Ivermectin Receptors
title_sort causal interrogation of neuronal networks and behavior through virally transduced ivermectin receptors
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5004486/
https://www.ncbi.nlm.nih.gov/pubmed/27625595
http://dx.doi.org/10.3389/fnmol.2016.00075
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