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Reconciling functional differences in populations of neurons recorded with two-photon imaging and electrophysiology

Extracellular electrophysiology and two-photon calcium imaging are widely used methods for measuring physiological activity with single-cell resolution across large populations of cortical neurons. While each of these two modalities has distinct advantages and disadvantages, neither provides complet...

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Autores principales: Siegle, Joshua H, Ledochowitsch, Peter, Jia, Xiaoxuan, Millman, Daniel J, Ocker, Gabriel K, Caldejon, Shiella, Casal, Linzy, Cho, Andy, Denman, Daniel J, Durand, Séverine, Groblewski, Peter A, Heller, Gregg, Kato, India, Kivikas, Sara, Lecoq, Jérôme, Nayan, Chelsea, Ngo, Kiet, Nicovich, Philip R, North, Kat, Ramirez, Tamina K, Swapp, Jackie, Waughman, Xana, Williford, Ali, Olsen, Shawn R, Koch, Christof, Buice, Michael A, de Vries, Saskia EJ
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8285106/
https://www.ncbi.nlm.nih.gov/pubmed/34270411
http://dx.doi.org/10.7554/eLife.69068
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author Siegle, Joshua H
Ledochowitsch, Peter
Jia, Xiaoxuan
Millman, Daniel J
Ocker, Gabriel K
Caldejon, Shiella
Casal, Linzy
Cho, Andy
Denman, Daniel J
Durand, Séverine
Groblewski, Peter A
Heller, Gregg
Kato, India
Kivikas, Sara
Lecoq, Jérôme
Nayan, Chelsea
Ngo, Kiet
Nicovich, Philip R
North, Kat
Ramirez, Tamina K
Swapp, Jackie
Waughman, Xana
Williford, Ali
Olsen, Shawn R
Koch, Christof
Buice, Michael A
de Vries, Saskia EJ
author_facet Siegle, Joshua H
Ledochowitsch, Peter
Jia, Xiaoxuan
Millman, Daniel J
Ocker, Gabriel K
Caldejon, Shiella
Casal, Linzy
Cho, Andy
Denman, Daniel J
Durand, Séverine
Groblewski, Peter A
Heller, Gregg
Kato, India
Kivikas, Sara
Lecoq, Jérôme
Nayan, Chelsea
Ngo, Kiet
Nicovich, Philip R
North, Kat
Ramirez, Tamina K
Swapp, Jackie
Waughman, Xana
Williford, Ali
Olsen, Shawn R
Koch, Christof
Buice, Michael A
de Vries, Saskia EJ
author_sort Siegle, Joshua H
collection PubMed
description Extracellular electrophysiology and two-photon calcium imaging are widely used methods for measuring physiological activity with single-cell resolution across large populations of cortical neurons. While each of these two modalities has distinct advantages and disadvantages, neither provides complete, unbiased information about the underlying neural population. Here, we compare evoked responses in visual cortex recorded in awake mice under highly standardized conditions using either imaging of genetically expressed GCaMP6f or electrophysiology with silicon probes. Across all stimulus conditions tested, we observe a larger fraction of responsive neurons in electrophysiology and higher stimulus selectivity in calcium imaging, which was partially reconciled by applying a spikes-to-calcium forward model to the electrophysiology data. However, the forward model could only reconcile differences in responsiveness when restricted to neurons with low contamination and an event rate above a minimum threshold. This work established how the biases of these two modalities impact functional metrics that are fundamental for characterizing sensory-evoked responses.
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spelling pubmed-82851062021-07-19 Reconciling functional differences in populations of neurons recorded with two-photon imaging and electrophysiology Siegle, Joshua H Ledochowitsch, Peter Jia, Xiaoxuan Millman, Daniel J Ocker, Gabriel K Caldejon, Shiella Casal, Linzy Cho, Andy Denman, Daniel J Durand, Séverine Groblewski, Peter A Heller, Gregg Kato, India Kivikas, Sara Lecoq, Jérôme Nayan, Chelsea Ngo, Kiet Nicovich, Philip R North, Kat Ramirez, Tamina K Swapp, Jackie Waughman, Xana Williford, Ali Olsen, Shawn R Koch, Christof Buice, Michael A de Vries, Saskia EJ eLife Neuroscience Extracellular electrophysiology and two-photon calcium imaging are widely used methods for measuring physiological activity with single-cell resolution across large populations of cortical neurons. While each of these two modalities has distinct advantages and disadvantages, neither provides complete, unbiased information about the underlying neural population. Here, we compare evoked responses in visual cortex recorded in awake mice under highly standardized conditions using either imaging of genetically expressed GCaMP6f or electrophysiology with silicon probes. Across all stimulus conditions tested, we observe a larger fraction of responsive neurons in electrophysiology and higher stimulus selectivity in calcium imaging, which was partially reconciled by applying a spikes-to-calcium forward model to the electrophysiology data. However, the forward model could only reconcile differences in responsiveness when restricted to neurons with low contamination and an event rate above a minimum threshold. This work established how the biases of these two modalities impact functional metrics that are fundamental for characterizing sensory-evoked responses. eLife Sciences Publications, Ltd 2021-07-16 /pmc/articles/PMC8285106/ /pubmed/34270411 http://dx.doi.org/10.7554/eLife.69068 Text en © 2021, Siegle et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Siegle, Joshua H
Ledochowitsch, Peter
Jia, Xiaoxuan
Millman, Daniel J
Ocker, Gabriel K
Caldejon, Shiella
Casal, Linzy
Cho, Andy
Denman, Daniel J
Durand, Séverine
Groblewski, Peter A
Heller, Gregg
Kato, India
Kivikas, Sara
Lecoq, Jérôme
Nayan, Chelsea
Ngo, Kiet
Nicovich, Philip R
North, Kat
Ramirez, Tamina K
Swapp, Jackie
Waughman, Xana
Williford, Ali
Olsen, Shawn R
Koch, Christof
Buice, Michael A
de Vries, Saskia EJ
Reconciling functional differences in populations of neurons recorded with two-photon imaging and electrophysiology
title Reconciling functional differences in populations of neurons recorded with two-photon imaging and electrophysiology
title_full Reconciling functional differences in populations of neurons recorded with two-photon imaging and electrophysiology
title_fullStr Reconciling functional differences in populations of neurons recorded with two-photon imaging and electrophysiology
title_full_unstemmed Reconciling functional differences in populations of neurons recorded with two-photon imaging and electrophysiology
title_short Reconciling functional differences in populations of neurons recorded with two-photon imaging and electrophysiology
title_sort reconciling functional differences in populations of neurons recorded with two-photon imaging and electrophysiology
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8285106/
https://www.ncbi.nlm.nih.gov/pubmed/34270411
http://dx.doi.org/10.7554/eLife.69068
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