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Degenerated Cones in Cultured Human Retinas Can Successfully Be Optogenetically Reactivated

Biblical references aside, restoring vision to the blind has proven to be a major technical challenge. In recent years, considerable advances have been made towards this end, especially when retinal degeneration underlies the vision loss such as occurs with retinitis pigmentosa. Under these conditio...

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Autores principales: Kamar, Sizar, Howlett, Marcus H. C., Klooster, Jan, de Graaff, Wim, Csikós, Tamás, Rabelink, Martijn J. W. E., Hoeben, Rob C., Kamermans, Maarten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7014344/
https://www.ncbi.nlm.nih.gov/pubmed/31947650
http://dx.doi.org/10.3390/ijms21020522
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author Kamar, Sizar
Howlett, Marcus H. C.
Klooster, Jan
de Graaff, Wim
Csikós, Tamás
Rabelink, Martijn J. W. E.
Hoeben, Rob C.
Kamermans, Maarten
author_facet Kamar, Sizar
Howlett, Marcus H. C.
Klooster, Jan
de Graaff, Wim
Csikós, Tamás
Rabelink, Martijn J. W. E.
Hoeben, Rob C.
Kamermans, Maarten
author_sort Kamar, Sizar
collection PubMed
description Biblical references aside, restoring vision to the blind has proven to be a major technical challenge. In recent years, considerable advances have been made towards this end, especially when retinal degeneration underlies the vision loss such as occurs with retinitis pigmentosa. Under these conditions, optogenetic therapies are a particularly promising line of inquiry where remaining retinal cells are made into “artificial photoreceptors”. However, this strategy is not without its challenges and a model system using human retinal explants would aid its continued development and refinement. Here, we cultured post-mortem human retinas and show that explants remain viable for around 7 days. Within this period, the cones lose their outer segments and thus their light sensitivity but remain electrophysiologically intact, displaying all the major ionic conductances one would expect for a vertebrate cone. We optogenetically restored light responses to these quiescent cones using a lentivirus vector constructed to express enhanced halorhodopsin under the control of the human arrestin promotor. In these ‘reactivated’ retinas, we show a light-induced horizontal cell to cone feedback signal in cones, indicating that transduced cones were able to transmit their light response across the synapse to horizontal cells, which generated a large enough response to send a signal back to the cones. Furthermore, we show ganglion cell light responses, suggesting the cultured explant’s condition is still good enough to support transmission of the transduced cone signal over the intermediate retinal layers to the final retinal output level. Together, these results show that cultured human retinas are an appropriate model system to test optogenetic vision restoration approaches and that cones which have lost their outer segment, a condition occurring during the early stages of retinitis pigmentosa, are appropriate targets for optogenetic vision restoration therapies.
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spelling pubmed-70143442020-03-09 Degenerated Cones in Cultured Human Retinas Can Successfully Be Optogenetically Reactivated Kamar, Sizar Howlett, Marcus H. C. Klooster, Jan de Graaff, Wim Csikós, Tamás Rabelink, Martijn J. W. E. Hoeben, Rob C. Kamermans, Maarten Int J Mol Sci Article Biblical references aside, restoring vision to the blind has proven to be a major technical challenge. In recent years, considerable advances have been made towards this end, especially when retinal degeneration underlies the vision loss such as occurs with retinitis pigmentosa. Under these conditions, optogenetic therapies are a particularly promising line of inquiry where remaining retinal cells are made into “artificial photoreceptors”. However, this strategy is not without its challenges and a model system using human retinal explants would aid its continued development and refinement. Here, we cultured post-mortem human retinas and show that explants remain viable for around 7 days. Within this period, the cones lose their outer segments and thus their light sensitivity but remain electrophysiologically intact, displaying all the major ionic conductances one would expect for a vertebrate cone. We optogenetically restored light responses to these quiescent cones using a lentivirus vector constructed to express enhanced halorhodopsin under the control of the human arrestin promotor. In these ‘reactivated’ retinas, we show a light-induced horizontal cell to cone feedback signal in cones, indicating that transduced cones were able to transmit their light response across the synapse to horizontal cells, which generated a large enough response to send a signal back to the cones. Furthermore, we show ganglion cell light responses, suggesting the cultured explant’s condition is still good enough to support transmission of the transduced cone signal over the intermediate retinal layers to the final retinal output level. Together, these results show that cultured human retinas are an appropriate model system to test optogenetic vision restoration approaches and that cones which have lost their outer segment, a condition occurring during the early stages of retinitis pigmentosa, are appropriate targets for optogenetic vision restoration therapies. MDPI 2020-01-14 /pmc/articles/PMC7014344/ /pubmed/31947650 http://dx.doi.org/10.3390/ijms21020522 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kamar, Sizar
Howlett, Marcus H. C.
Klooster, Jan
de Graaff, Wim
Csikós, Tamás
Rabelink, Martijn J. W. E.
Hoeben, Rob C.
Kamermans, Maarten
Degenerated Cones in Cultured Human Retinas Can Successfully Be Optogenetically Reactivated
title Degenerated Cones in Cultured Human Retinas Can Successfully Be Optogenetically Reactivated
title_full Degenerated Cones in Cultured Human Retinas Can Successfully Be Optogenetically Reactivated
title_fullStr Degenerated Cones in Cultured Human Retinas Can Successfully Be Optogenetically Reactivated
title_full_unstemmed Degenerated Cones in Cultured Human Retinas Can Successfully Be Optogenetically Reactivated
title_short Degenerated Cones in Cultured Human Retinas Can Successfully Be Optogenetically Reactivated
title_sort degenerated cones in cultured human retinas can successfully be optogenetically reactivated
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7014344/
https://www.ncbi.nlm.nih.gov/pubmed/31947650
http://dx.doi.org/10.3390/ijms21020522
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