Laserspritzer: a simple method for optogenetic investigation with subcellular resolutions.

To build a detailed circuit diagram in the brain, one needs to measure functional synaptic connections between specific types of neurons. A high-resolution circuit diagram should provide detailed information at subcellular levels such as soma, distal and basal dendrites. However, a limitation lies i...

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Main Authors: Qian-Quan Sun, Xinjun Wang, Weiguo Yang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4081651?pdf=render
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spelling doaj-0cc1924edce241208af00c0409c348722020-11-25T01:17:14ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0197e10160010.1371/journal.pone.0101600Laserspritzer: a simple method for optogenetic investigation with subcellular resolutions.Qian-Quan SunXinjun WangWeiguo YangTo build a detailed circuit diagram in the brain, one needs to measure functional synaptic connections between specific types of neurons. A high-resolution circuit diagram should provide detailed information at subcellular levels such as soma, distal and basal dendrites. However, a limitation lies in the difficulty of studying long-range connections between brain areas separated by millimeters. Brain slice preparations have been widely used to help understand circuit wiring within specific brain regions. The challenge exists because long-range connections are likely to be cut in a brain slice. The optogenetic approach overcomes these limitations, as channelrhodopsin 2 (ChR2) is efficiently transported to axon terminals that can be stimulated in brain slices. Here, we developed a novel fiber optic based simple method of optogenetic stimulation: the laserspritzer approach. This method facilitates the study of both long-range and local circuits within brain slice preparations. This is a convenient and low cost approach that can be easily integrated with a slice electrophysiology setup, and repeatedly used upon initial validation. Our data with direct ChR2 mediated-current recordings demonstrates that the spatial resolution of the laserspritzer is correlated with the size of the laserspritzer, and the resolution lies within the 30 µm range for the 5 micrometer laserspritzer. Using olfactory cortical slices, we demonstrated that the laserspritzer approach can be applied to selectively activate monosynaptic perisomatic GABAergic basket synapses, or long-range intracortical glutamatergic inputs formed on different subcellular domains within the same cell (e.g. distal and proximal dendrites). We discuss significant advantages of the laserspritzer approach over the widely used collimated LED whole-field illumination method in brain slice electrophysiological research.http://europepmc.org/articles/PMC4081651?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Qian-Quan Sun
Xinjun Wang
Weiguo Yang
spellingShingle Qian-Quan Sun
Xinjun Wang
Weiguo Yang
Laserspritzer: a simple method for optogenetic investigation with subcellular resolutions.
PLoS ONE
author_facet Qian-Quan Sun
Xinjun Wang
Weiguo Yang
author_sort Qian-Quan Sun
title Laserspritzer: a simple method for optogenetic investigation with subcellular resolutions.
title_short Laserspritzer: a simple method for optogenetic investigation with subcellular resolutions.
title_full Laserspritzer: a simple method for optogenetic investigation with subcellular resolutions.
title_fullStr Laserspritzer: a simple method for optogenetic investigation with subcellular resolutions.
title_full_unstemmed Laserspritzer: a simple method for optogenetic investigation with subcellular resolutions.
title_sort laserspritzer: a simple method for optogenetic investigation with subcellular resolutions.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description To build a detailed circuit diagram in the brain, one needs to measure functional synaptic connections between specific types of neurons. A high-resolution circuit diagram should provide detailed information at subcellular levels such as soma, distal and basal dendrites. However, a limitation lies in the difficulty of studying long-range connections between brain areas separated by millimeters. Brain slice preparations have been widely used to help understand circuit wiring within specific brain regions. The challenge exists because long-range connections are likely to be cut in a brain slice. The optogenetic approach overcomes these limitations, as channelrhodopsin 2 (ChR2) is efficiently transported to axon terminals that can be stimulated in brain slices. Here, we developed a novel fiber optic based simple method of optogenetic stimulation: the laserspritzer approach. This method facilitates the study of both long-range and local circuits within brain slice preparations. This is a convenient and low cost approach that can be easily integrated with a slice electrophysiology setup, and repeatedly used upon initial validation. Our data with direct ChR2 mediated-current recordings demonstrates that the spatial resolution of the laserspritzer is correlated with the size of the laserspritzer, and the resolution lies within the 30 µm range for the 5 micrometer laserspritzer. Using olfactory cortical slices, we demonstrated that the laserspritzer approach can be applied to selectively activate monosynaptic perisomatic GABAergic basket synapses, or long-range intracortical glutamatergic inputs formed on different subcellular domains within the same cell (e.g. distal and proximal dendrites). We discuss significant advantages of the laserspritzer approach over the widely used collimated LED whole-field illumination method in brain slice electrophysiological research.
url http://europepmc.org/articles/PMC4081651?pdf=render
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AT xinjunwang laserspritzerasimplemethodforoptogeneticinvestigationwithsubcellularresolutions
AT weiguoyang laserspritzerasimplemethodforoptogeneticinvestigationwithsubcellularresolutions
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