Cargando…

Utility of red‐light ultrafast optogenetic stimulation of the auditory pathway

Optogenetic stimulation of spiral ganglion neurons (SGNs) in the ear provides a future alternative to electrical stimulation used in current cochlear implants. Here, we employed fast and very fast variants of the red‐light‐activated channelrhodopsin (ChR) Chrimson (f‐Chrimson and vf‐Chrimson) to stu...

Descripción completa

Detalles Bibliográficos
Autores principales: Bali, Burak, Lopez de la Morena, David, Mittring, Artur, Mager, Thomas, Rankovic, Vladan, Huet, Antoine Tarquin, Moser, Tobias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8185542/
https://www.ncbi.nlm.nih.gov/pubmed/33960685
http://dx.doi.org/10.15252/emmm.202013391
_version_ 1783704810048978944
author Bali, Burak
Lopez de la Morena, David
Mittring, Artur
Mager, Thomas
Rankovic, Vladan
Huet, Antoine Tarquin
Moser, Tobias
author_facet Bali, Burak
Lopez de la Morena, David
Mittring, Artur
Mager, Thomas
Rankovic, Vladan
Huet, Antoine Tarquin
Moser, Tobias
author_sort Bali, Burak
collection PubMed
description Optogenetic stimulation of spiral ganglion neurons (SGNs) in the ear provides a future alternative to electrical stimulation used in current cochlear implants. Here, we employed fast and very fast variants of the red‐light‐activated channelrhodopsin (ChR) Chrimson (f‐Chrimson and vf‐Chrimson) to study their utility for optogenetic stimulation of SGNs in mice. The light requirements were higher for vf‐Chrimson than for f‐Chrimson, even when optimizing membrane expression of vf‐Chrimson by adding potassium channel trafficking sequences. Optogenetic time and intensity coding by single putative SGNs were compared with coding of acoustic clicks. vf‐Chrimson enabled putative SGNs to fire at near‐physiological rates with good temporal precision up to 250 Hz of stimulation. The dynamic range of SGN spike rate coding upon optogenetic stimulation was narrower than for acoustic clicks but larger than reported for electrical stimulation. The dynamic range of spike timing, on the other hand, was more comparable for optogenetic and acoustic stimulation. In conclusion, f‐Chrimson and vf‐Chrimson are promising candidates for optogenetic stimulation of SGNs in auditory research and future cochlear implants.
format Online
Article
Text
id pubmed-8185542
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-81855422021-06-15 Utility of red‐light ultrafast optogenetic stimulation of the auditory pathway Bali, Burak Lopez de la Morena, David Mittring, Artur Mager, Thomas Rankovic, Vladan Huet, Antoine Tarquin Moser, Tobias EMBO Mol Med Articles Optogenetic stimulation of spiral ganglion neurons (SGNs) in the ear provides a future alternative to electrical stimulation used in current cochlear implants. Here, we employed fast and very fast variants of the red‐light‐activated channelrhodopsin (ChR) Chrimson (f‐Chrimson and vf‐Chrimson) to study their utility for optogenetic stimulation of SGNs in mice. The light requirements were higher for vf‐Chrimson than for f‐Chrimson, even when optimizing membrane expression of vf‐Chrimson by adding potassium channel trafficking sequences. Optogenetic time and intensity coding by single putative SGNs were compared with coding of acoustic clicks. vf‐Chrimson enabled putative SGNs to fire at near‐physiological rates with good temporal precision up to 250 Hz of stimulation. The dynamic range of SGN spike rate coding upon optogenetic stimulation was narrower than for acoustic clicks but larger than reported for electrical stimulation. The dynamic range of spike timing, on the other hand, was more comparable for optogenetic and acoustic stimulation. In conclusion, f‐Chrimson and vf‐Chrimson are promising candidates for optogenetic stimulation of SGNs in auditory research and future cochlear implants. John Wiley and Sons Inc. 2021-05-07 2021-06-08 /pmc/articles/PMC8185542/ /pubmed/33960685 http://dx.doi.org/10.15252/emmm.202013391 Text en © 2021 The Authors. Published under the terms of the CC BY 4.0 license https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Bali, Burak
Lopez de la Morena, David
Mittring, Artur
Mager, Thomas
Rankovic, Vladan
Huet, Antoine Tarquin
Moser, Tobias
Utility of red‐light ultrafast optogenetic stimulation of the auditory pathway
title Utility of red‐light ultrafast optogenetic stimulation of the auditory pathway
title_full Utility of red‐light ultrafast optogenetic stimulation of the auditory pathway
title_fullStr Utility of red‐light ultrafast optogenetic stimulation of the auditory pathway
title_full_unstemmed Utility of red‐light ultrafast optogenetic stimulation of the auditory pathway
title_short Utility of red‐light ultrafast optogenetic stimulation of the auditory pathway
title_sort utility of red‐light ultrafast optogenetic stimulation of the auditory pathway
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8185542/
https://www.ncbi.nlm.nih.gov/pubmed/33960685
http://dx.doi.org/10.15252/emmm.202013391
work_keys_str_mv AT baliburak utilityofredlightultrafastoptogeneticstimulationoftheauditorypathway
AT lopezdelamorenadavid utilityofredlightultrafastoptogeneticstimulationoftheauditorypathway
AT mittringartur utilityofredlightultrafastoptogeneticstimulationoftheauditorypathway
AT magerthomas utilityofredlightultrafastoptogeneticstimulationoftheauditorypathway
AT rankovicvladan utilityofredlightultrafastoptogeneticstimulationoftheauditorypathway
AT huetantoinetarquin utilityofredlightultrafastoptogeneticstimulationoftheauditorypathway
AT mosertobias utilityofredlightultrafastoptogeneticstimulationoftheauditorypathway