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Two-Photon Optogenetic Mapping of Excitatory Synaptic Connectivity and Strength

The development of optical methods to activate neurons with single-cell resolution has enabled systematic mapping of inhibitory connections. In contrast, optical mapping of excitatory connections between pyramidal neurons (PCs) has been a major challenge due to their high densities in cortical tissu...

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Autores principales: Izquierdo-Serra, Mercè, Hirtz, Jan J., Shababo, Ben, Yuste, Rafael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6170329/
https://www.ncbi.nlm.nih.gov/pubmed/30268510
http://dx.doi.org/10.1016/j.isci.2018.09.008
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author Izquierdo-Serra, Mercè
Hirtz, Jan J.
Shababo, Ben
Yuste, Rafael
author_facet Izquierdo-Serra, Mercè
Hirtz, Jan J.
Shababo, Ben
Yuste, Rafael
author_sort Izquierdo-Serra, Mercè
collection PubMed
description The development of optical methods to activate neurons with single-cell resolution has enabled systematic mapping of inhibitory connections. In contrast, optical mapping of excitatory connections between pyramidal neurons (PCs) has been a major challenge due to their high densities in cortical tissue and their weak and stochastic connectivity. Here we present an optogenetic two-photon mapping method in mouse neocortical slices by activating PCs with the red-shifted opsin C1V1 while recording postsynaptic responses in whole-cell configuration. Comparison of delays from triggered action potentials (APs) with those from synaptic inputs allowed us to predict connected PCs in three dimensions. We confirmed these predictions with paired recordings, and used this method to map strong connections among large populations of layer 2/3 PCs. Our method can be used for fast, systematic mapping of synaptic connectivity and weights.
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spelling pubmed-61703292018-10-05 Two-Photon Optogenetic Mapping of Excitatory Synaptic Connectivity and Strength Izquierdo-Serra, Mercè Hirtz, Jan J. Shababo, Ben Yuste, Rafael iScience Article The development of optical methods to activate neurons with single-cell resolution has enabled systematic mapping of inhibitory connections. In contrast, optical mapping of excitatory connections between pyramidal neurons (PCs) has been a major challenge due to their high densities in cortical tissue and their weak and stochastic connectivity. Here we present an optogenetic two-photon mapping method in mouse neocortical slices by activating PCs with the red-shifted opsin C1V1 while recording postsynaptic responses in whole-cell configuration. Comparison of delays from triggered action potentials (APs) with those from synaptic inputs allowed us to predict connected PCs in three dimensions. We confirmed these predictions with paired recordings, and used this method to map strong connections among large populations of layer 2/3 PCs. Our method can be used for fast, systematic mapping of synaptic connectivity and weights. Elsevier 2018-09-13 /pmc/articles/PMC6170329/ /pubmed/30268510 http://dx.doi.org/10.1016/j.isci.2018.09.008 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Izquierdo-Serra, Mercè
Hirtz, Jan J.
Shababo, Ben
Yuste, Rafael
Two-Photon Optogenetic Mapping of Excitatory Synaptic Connectivity and Strength
title Two-Photon Optogenetic Mapping of Excitatory Synaptic Connectivity and Strength
title_full Two-Photon Optogenetic Mapping of Excitatory Synaptic Connectivity and Strength
title_fullStr Two-Photon Optogenetic Mapping of Excitatory Synaptic Connectivity and Strength
title_full_unstemmed Two-Photon Optogenetic Mapping of Excitatory Synaptic Connectivity and Strength
title_short Two-Photon Optogenetic Mapping of Excitatory Synaptic Connectivity and Strength
title_sort two-photon optogenetic mapping of excitatory synaptic connectivity and strength
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6170329/
https://www.ncbi.nlm.nih.gov/pubmed/30268510
http://dx.doi.org/10.1016/j.isci.2018.09.008
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