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Dissecting inhibitory brain circuits with genetically-targeted technologies

The evolution of genetically targeted tools has begun to allow us to dissect anatomically and functionally heterogeneous interneurons, and to probe circuit function from synapses to behavior. Over the last decade, these tools have been used widely to visualize neurons in a cell type-specific manner,...

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Detalles Bibliográficos
Autores principales: Murphey, Dona K., Herman, Alexander M., Arenkiel, Benjamin R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4201106/
https://www.ncbi.nlm.nih.gov/pubmed/25368555
http://dx.doi.org/10.3389/fncir.2014.00124
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author Murphey, Dona K.
Herman, Alexander M.
Arenkiel, Benjamin R.
author_facet Murphey, Dona K.
Herman, Alexander M.
Arenkiel, Benjamin R.
author_sort Murphey, Dona K.
collection PubMed
description The evolution of genetically targeted tools has begun to allow us to dissect anatomically and functionally heterogeneous interneurons, and to probe circuit function from synapses to behavior. Over the last decade, these tools have been used widely to visualize neurons in a cell type-specific manner, and engage them to activate and inactivate with exquisite precision. In this process, we have expanded our understanding of interneuron diversity, their functional connectivity, and how selective inhibitory circuits contribute to behavior. Here we discuss the relative assets of genetically encoded fluorescent proteins (FPs), viral tracing methods, optogenetics, chemical genetics, and biosensors in the study of inhibitory interneurons and their respective circuits.
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spelling pubmed-42011062014-11-03 Dissecting inhibitory brain circuits with genetically-targeted technologies Murphey, Dona K. Herman, Alexander M. Arenkiel, Benjamin R. Front Neural Circuits Neuroscience The evolution of genetically targeted tools has begun to allow us to dissect anatomically and functionally heterogeneous interneurons, and to probe circuit function from synapses to behavior. Over the last decade, these tools have been used widely to visualize neurons in a cell type-specific manner, and engage them to activate and inactivate with exquisite precision. In this process, we have expanded our understanding of interneuron diversity, their functional connectivity, and how selective inhibitory circuits contribute to behavior. Here we discuss the relative assets of genetically encoded fluorescent proteins (FPs), viral tracing methods, optogenetics, chemical genetics, and biosensors in the study of inhibitory interneurons and their respective circuits. Frontiers Media S.A. 2014-10-17 /pmc/articles/PMC4201106/ /pubmed/25368555 http://dx.doi.org/10.3389/fncir.2014.00124 Text en Copyright © 2014 Murphey, Herman and Arenkiel. 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
Murphey, Dona K.
Herman, Alexander M.
Arenkiel, Benjamin R.
Dissecting inhibitory brain circuits with genetically-targeted technologies
title Dissecting inhibitory brain circuits with genetically-targeted technologies
title_full Dissecting inhibitory brain circuits with genetically-targeted technologies
title_fullStr Dissecting inhibitory brain circuits with genetically-targeted technologies
title_full_unstemmed Dissecting inhibitory brain circuits with genetically-targeted technologies
title_short Dissecting inhibitory brain circuits with genetically-targeted technologies
title_sort dissecting inhibitory brain circuits with genetically-targeted technologies
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4201106/
https://www.ncbi.nlm.nih.gov/pubmed/25368555
http://dx.doi.org/10.3389/fncir.2014.00124
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