Cargando…

Thy1 transgenic mice expressing the red fluorescent calcium indicator jRGECO1a for neuronal population imaging in vivo

Calcium imaging is commonly used to measure the neural activity of large groups of neurons in mice. Genetically encoded calcium indicators (GECIs) can be delivered for this purpose using non-invasive genetic methods. Compared to viral gene transfer, transgenic targeting of GECIs provides stable long...

Descripción completa

Detalles Bibliográficos
Autores principales: Dana, Hod, Novak, Ondrej, Guardado-Montesino, Michael, Fransen, James W., Hu, Amy, Borghuis, Bart G., Guo, Caiying, Kim, Douglas S., Svoboda, Karel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6181368/
https://www.ncbi.nlm.nih.gov/pubmed/30308007
http://dx.doi.org/10.1371/journal.pone.0205444
_version_ 1783362384075685888
author Dana, Hod
Novak, Ondrej
Guardado-Montesino, Michael
Fransen, James W.
Hu, Amy
Borghuis, Bart G.
Guo, Caiying
Kim, Douglas S.
Svoboda, Karel
author_facet Dana, Hod
Novak, Ondrej
Guardado-Montesino, Michael
Fransen, James W.
Hu, Amy
Borghuis, Bart G.
Guo, Caiying
Kim, Douglas S.
Svoboda, Karel
author_sort Dana, Hod
collection PubMed
description Calcium imaging is commonly used to measure the neural activity of large groups of neurons in mice. Genetically encoded calcium indicators (GECIs) can be delivered for this purpose using non-invasive genetic methods. Compared to viral gene transfer, transgenic targeting of GECIs provides stable long-term expression and obviates the need for invasive viral injections. Transgenic mice expressing the green GECI GCaMP6 are already widely used. Here we present the generation and characterization of transgenic mice expressing the sensitive red GECI jRGECO1a, driven by the Thy1 promoter. Four transgenic lines with different expression patterns showed sufficiently high expression for cellular in vivo imaging. We used two-photon microscopy to characterize visual responses of individual neurons in the visual cortex in vivo. The signal-to-noise ratio in transgenic mice was comparable to, or better than, mice transduced with adeno-associated virus. In addition, we show that Thy1-jRGECO1a transgenic mice are useful for transcranial population imaging and functional mapping using widefield fluorescence microscopy. We also demonstrate imaging of visual responses in retinal ganglion cells in vitro. Thy1-jRGECO1a transgenic mice are therefore a useful addition to the toolbox for imaging activity in intact neural networks.
format Online
Article
Text
id pubmed-6181368
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-61813682018-10-26 Thy1 transgenic mice expressing the red fluorescent calcium indicator jRGECO1a for neuronal population imaging in vivo Dana, Hod Novak, Ondrej Guardado-Montesino, Michael Fransen, James W. Hu, Amy Borghuis, Bart G. Guo, Caiying Kim, Douglas S. Svoboda, Karel PLoS One Research Article Calcium imaging is commonly used to measure the neural activity of large groups of neurons in mice. Genetically encoded calcium indicators (GECIs) can be delivered for this purpose using non-invasive genetic methods. Compared to viral gene transfer, transgenic targeting of GECIs provides stable long-term expression and obviates the need for invasive viral injections. Transgenic mice expressing the green GECI GCaMP6 are already widely used. Here we present the generation and characterization of transgenic mice expressing the sensitive red GECI jRGECO1a, driven by the Thy1 promoter. Four transgenic lines with different expression patterns showed sufficiently high expression for cellular in vivo imaging. We used two-photon microscopy to characterize visual responses of individual neurons in the visual cortex in vivo. The signal-to-noise ratio in transgenic mice was comparable to, or better than, mice transduced with adeno-associated virus. In addition, we show that Thy1-jRGECO1a transgenic mice are useful for transcranial population imaging and functional mapping using widefield fluorescence microscopy. We also demonstrate imaging of visual responses in retinal ganglion cells in vitro. Thy1-jRGECO1a transgenic mice are therefore a useful addition to the toolbox for imaging activity in intact neural networks. Public Library of Science 2018-10-11 /pmc/articles/PMC6181368/ /pubmed/30308007 http://dx.doi.org/10.1371/journal.pone.0205444 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Dana, Hod
Novak, Ondrej
Guardado-Montesino, Michael
Fransen, James W.
Hu, Amy
Borghuis, Bart G.
Guo, Caiying
Kim, Douglas S.
Svoboda, Karel
Thy1 transgenic mice expressing the red fluorescent calcium indicator jRGECO1a for neuronal population imaging in vivo
title Thy1 transgenic mice expressing the red fluorescent calcium indicator jRGECO1a for neuronal population imaging in vivo
title_full Thy1 transgenic mice expressing the red fluorescent calcium indicator jRGECO1a for neuronal population imaging in vivo
title_fullStr Thy1 transgenic mice expressing the red fluorescent calcium indicator jRGECO1a for neuronal population imaging in vivo
title_full_unstemmed Thy1 transgenic mice expressing the red fluorescent calcium indicator jRGECO1a for neuronal population imaging in vivo
title_short Thy1 transgenic mice expressing the red fluorescent calcium indicator jRGECO1a for neuronal population imaging in vivo
title_sort thy1 transgenic mice expressing the red fluorescent calcium indicator jrgeco1a for neuronal population imaging in vivo
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6181368/
https://www.ncbi.nlm.nih.gov/pubmed/30308007
http://dx.doi.org/10.1371/journal.pone.0205444
work_keys_str_mv AT danahod thy1transgenicmiceexpressingtheredfluorescentcalciumindicatorjrgeco1aforneuronalpopulationimaginginvivo
AT novakondrej thy1transgenicmiceexpressingtheredfluorescentcalciumindicatorjrgeco1aforneuronalpopulationimaginginvivo
AT guardadomontesinomichael thy1transgenicmiceexpressingtheredfluorescentcalciumindicatorjrgeco1aforneuronalpopulationimaginginvivo
AT fransenjamesw thy1transgenicmiceexpressingtheredfluorescentcalciumindicatorjrgeco1aforneuronalpopulationimaginginvivo
AT huamy thy1transgenicmiceexpressingtheredfluorescentcalciumindicatorjrgeco1aforneuronalpopulationimaginginvivo
AT borghuisbartg thy1transgenicmiceexpressingtheredfluorescentcalciumindicatorjrgeco1aforneuronalpopulationimaginginvivo
AT guocaiying thy1transgenicmiceexpressingtheredfluorescentcalciumindicatorjrgeco1aforneuronalpopulationimaginginvivo
AT kimdouglass thy1transgenicmiceexpressingtheredfluorescentcalciumindicatorjrgeco1aforneuronalpopulationimaginginvivo
AT svobodakarel thy1transgenicmiceexpressingtheredfluorescentcalciumindicatorjrgeco1aforneuronalpopulationimaginginvivo