Channelrhodopsin-Assisted Patching: In Vivo Recording of Genetically and Morphologically Identified Neurons throughout the Brain

Brain networks contain a large diversity of functionally distinct neuronal elements, each with unique properties, enabling computational capacities and supporting brain functions. Understanding their functional implications for behavior requires the precise identification of the cell types of a netw...

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Main Authors: William Muñoz, Robin Tremblay, Bernardo Rudy
Format: Article
Language:English
Published: Elsevier 2014-12-01
Series:Cell Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124714010080
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spelling doaj-6fcc6d2e8b374ad7b3845a579e71e1392020-11-25T01:13:26ZengElsevierCell Reports2211-12472014-12-01962304231610.1016/j.celrep.2014.11.042Channelrhodopsin-Assisted Patching: In Vivo Recording of Genetically and Morphologically Identified Neurons throughout the BrainWilliam Muñoz0Robin Tremblay1Bernardo Rudy2NYU Neuroscience Institute, NYU School of Medicine, New York, NY 10016, USANYU Neuroscience Institute, NYU School of Medicine, New York, NY 10016, USANYU Neuroscience Institute, NYU School of Medicine, New York, NY 10016, USABrain networks contain a large diversity of functionally distinct neuronal elements, each with unique properties, enabling computational capacities and supporting brain functions. Understanding their functional implications for behavior requires the precise identification of the cell types of a network and in vivo monitoring of their activity profiles. Here, we developed a channelrhodopsin-assisted patching method allowing the efficient in vivo targeted recording of neurons identified by their molecular, electrophysiological, and morphological features. The method has a high yield, does not require visual guidance, and thus can be applied at any depth in the brain. This approach overcomes limitations of present technologies. We validate this strategy with in vivo recordings of identified subtypes of GABAergic and glutamatergic neurons in deep cortical layers, subcortical cholinergic neurons, and neurons in the thalamic reticular nucleus in anesthetized and awake mice. We propose this method as an important complement to existing technologies to relate specific cell-type activity to brain circuitry, function, and behavior.http://www.sciencedirect.com/science/article/pii/S2211124714010080
collection DOAJ
language English
format Article
sources DOAJ
author William Muñoz
Robin Tremblay
Bernardo Rudy
spellingShingle William Muñoz
Robin Tremblay
Bernardo Rudy
Channelrhodopsin-Assisted Patching: In Vivo Recording of Genetically and Morphologically Identified Neurons throughout the Brain
Cell Reports
author_facet William Muñoz
Robin Tremblay
Bernardo Rudy
author_sort William Muñoz
title Channelrhodopsin-Assisted Patching: In Vivo Recording of Genetically and Morphologically Identified Neurons throughout the Brain
title_short Channelrhodopsin-Assisted Patching: In Vivo Recording of Genetically and Morphologically Identified Neurons throughout the Brain
title_full Channelrhodopsin-Assisted Patching: In Vivo Recording of Genetically and Morphologically Identified Neurons throughout the Brain
title_fullStr Channelrhodopsin-Assisted Patching: In Vivo Recording of Genetically and Morphologically Identified Neurons throughout the Brain
title_full_unstemmed Channelrhodopsin-Assisted Patching: In Vivo Recording of Genetically and Morphologically Identified Neurons throughout the Brain
title_sort channelrhodopsin-assisted patching: in vivo recording of genetically and morphologically identified neurons throughout the brain
publisher Elsevier
series Cell Reports
issn 2211-1247
publishDate 2014-12-01
description Brain networks contain a large diversity of functionally distinct neuronal elements, each with unique properties, enabling computational capacities and supporting brain functions. Understanding their functional implications for behavior requires the precise identification of the cell types of a network and in vivo monitoring of their activity profiles. Here, we developed a channelrhodopsin-assisted patching method allowing the efficient in vivo targeted recording of neurons identified by their molecular, electrophysiological, and morphological features. The method has a high yield, does not require visual guidance, and thus can be applied at any depth in the brain. This approach overcomes limitations of present technologies. We validate this strategy with in vivo recordings of identified subtypes of GABAergic and glutamatergic neurons in deep cortical layers, subcortical cholinergic neurons, and neurons in the thalamic reticular nucleus in anesthetized and awake mice. We propose this method as an important complement to existing technologies to relate specific cell-type activity to brain circuitry, function, and behavior.
url http://www.sciencedirect.com/science/article/pii/S2211124714010080
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