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Optical inhibition of larval zebrafish behaviour with anion channelrhodopsins

BACKGROUND: Optical silencing of activity provides a way to test the necessity of neurons in behaviour. Two light-gated anion channels, GtACR1 and GtACR2, have recently been shown to potently inhibit activity in cultured mammalian neurons and in Drosophila. Here, we test the usefulness of these chan...

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Autores principales: Mohamed, Gadisti Aisha, Cheng, Ruey-Kuang, Ho, Joses, Krishnan, Seetha, Mohammad, Farhan, Claridge-Chang, Adam, Jesuthasan, Suresh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5670698/
https://www.ncbi.nlm.nih.gov/pubmed/29100505
http://dx.doi.org/10.1186/s12915-017-0430-2
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author Mohamed, Gadisti Aisha
Cheng, Ruey-Kuang
Ho, Joses
Krishnan, Seetha
Mohammad, Farhan
Claridge-Chang, Adam
Jesuthasan, Suresh
author_facet Mohamed, Gadisti Aisha
Cheng, Ruey-Kuang
Ho, Joses
Krishnan, Seetha
Mohammad, Farhan
Claridge-Chang, Adam
Jesuthasan, Suresh
author_sort Mohamed, Gadisti Aisha
collection PubMed
description BACKGROUND: Optical silencing of activity provides a way to test the necessity of neurons in behaviour. Two light-gated anion channels, GtACR1 and GtACR2, have recently been shown to potently inhibit activity in cultured mammalian neurons and in Drosophila. Here, we test the usefulness of these channels in larval zebrafish, using spontaneous coiling behaviour as the assay. RESULTS: When the GtACRs were expressed in spinal neurons of embryonic zebrafish and actuated with blue or green light, spontaneous movement was inhibited. In GtACR1-expressing fish, only 3 μW/mm(2) of light was sufficient to have an effect; GtACR2, which is poorly trafficked, required slightly stronger illumination. No inhibition was seen in non-expressing siblings. After light offset, the movement of GtACR-expressing fish increased, which suggested that termination of light-induced neural inhibition may lead to activation. Consistent with this, two-photon imaging of spinal neurons showed that blue light inhibited spontaneous activity in spinal neurons of GtACR1-expressing fish, and that the level of intracellular calcium increased following light offset. CONCLUSIONS: These results show that GtACR1 and GtACR2 can be used to optically inhibit neurons in larval zebrafish with high efficiency. The activity elicited at light offset needs to be taken into consideration in experimental design, although this property can provide insight into the effects of transiently stimulating a circuit. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-017-0430-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-56706982017-11-15 Optical inhibition of larval zebrafish behaviour with anion channelrhodopsins Mohamed, Gadisti Aisha Cheng, Ruey-Kuang Ho, Joses Krishnan, Seetha Mohammad, Farhan Claridge-Chang, Adam Jesuthasan, Suresh BMC Biol Methodology Article BACKGROUND: Optical silencing of activity provides a way to test the necessity of neurons in behaviour. Two light-gated anion channels, GtACR1 and GtACR2, have recently been shown to potently inhibit activity in cultured mammalian neurons and in Drosophila. Here, we test the usefulness of these channels in larval zebrafish, using spontaneous coiling behaviour as the assay. RESULTS: When the GtACRs were expressed in spinal neurons of embryonic zebrafish and actuated with blue or green light, spontaneous movement was inhibited. In GtACR1-expressing fish, only 3 μW/mm(2) of light was sufficient to have an effect; GtACR2, which is poorly trafficked, required slightly stronger illumination. No inhibition was seen in non-expressing siblings. After light offset, the movement of GtACR-expressing fish increased, which suggested that termination of light-induced neural inhibition may lead to activation. Consistent with this, two-photon imaging of spinal neurons showed that blue light inhibited spontaneous activity in spinal neurons of GtACR1-expressing fish, and that the level of intracellular calcium increased following light offset. CONCLUSIONS: These results show that GtACR1 and GtACR2 can be used to optically inhibit neurons in larval zebrafish with high efficiency. The activity elicited at light offset needs to be taken into consideration in experimental design, although this property can provide insight into the effects of transiently stimulating a circuit. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-017-0430-2) contains supplementary material, which is available to authorized users. BioMed Central 2017-11-03 /pmc/articles/PMC5670698/ /pubmed/29100505 http://dx.doi.org/10.1186/s12915-017-0430-2 Text en © Jesuthasan et al. 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Methodology Article
Mohamed, Gadisti Aisha
Cheng, Ruey-Kuang
Ho, Joses
Krishnan, Seetha
Mohammad, Farhan
Claridge-Chang, Adam
Jesuthasan, Suresh
Optical inhibition of larval zebrafish behaviour with anion channelrhodopsins
title Optical inhibition of larval zebrafish behaviour with anion channelrhodopsins
title_full Optical inhibition of larval zebrafish behaviour with anion channelrhodopsins
title_fullStr Optical inhibition of larval zebrafish behaviour with anion channelrhodopsins
title_full_unstemmed Optical inhibition of larval zebrafish behaviour with anion channelrhodopsins
title_short Optical inhibition of larval zebrafish behaviour with anion channelrhodopsins
title_sort optical inhibition of larval zebrafish behaviour with anion channelrhodopsins
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5670698/
https://www.ncbi.nlm.nih.gov/pubmed/29100505
http://dx.doi.org/10.1186/s12915-017-0430-2
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