Cargando…
Optogenetic restoration of retinal ganglion cell activity in the living primate
Optogenetic therapies for vision restoration aim to confer intrinsic light sensitivity to retinal ganglion cells when photoreceptors have degenerated and light sensitivity has been irreversibly lost. We combine adaptive optics ophthalmoscopy with calcium imaging to optically record optogenetically r...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7125151/ https://www.ncbi.nlm.nih.gov/pubmed/32245977 http://dx.doi.org/10.1038/s41467-020-15317-6 |
_version_ | 1783515888722378752 |
---|---|
author | McGregor, Juliette E. Godat, Tyler Dhakal, Kamal R. Parkins, Keith Strazzeri, Jennifer M. Bateman, Brittany A. Fischer, William S. Williams, David R. Merigan, William H. |
author_facet | McGregor, Juliette E. Godat, Tyler Dhakal, Kamal R. Parkins, Keith Strazzeri, Jennifer M. Bateman, Brittany A. Fischer, William S. Williams, David R. Merigan, William H. |
author_sort | McGregor, Juliette E. |
collection | PubMed |
description | Optogenetic therapies for vision restoration aim to confer intrinsic light sensitivity to retinal ganglion cells when photoreceptors have degenerated and light sensitivity has been irreversibly lost. We combine adaptive optics ophthalmoscopy with calcium imaging to optically record optogenetically restored retinal ganglion cell activity in the fovea of the living primate. Recording from the intact eye of a living animal, we compare the patterns of activity evoked by the optogenetic actuator ChrimsonR with natural photoreceptor mediated stimulation in the same retinal ganglion cells. Optogenetic responses are recorded more than one year following administration of the therapy and two weeks after acute loss of photoreceptor input in the living animal. This in vivo imaging approach could be paired with any therapy to minimize the number of primates required to evaluate restored activity on the retinal level, while maximizing translational benefit by using an appropriate pre-clinical model of the human visual system. |
format | Online Article Text |
id | pubmed-7125151 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-71251512020-04-06 Optogenetic restoration of retinal ganglion cell activity in the living primate McGregor, Juliette E. Godat, Tyler Dhakal, Kamal R. Parkins, Keith Strazzeri, Jennifer M. Bateman, Brittany A. Fischer, William S. Williams, David R. Merigan, William H. Nat Commun Article Optogenetic therapies for vision restoration aim to confer intrinsic light sensitivity to retinal ganglion cells when photoreceptors have degenerated and light sensitivity has been irreversibly lost. We combine adaptive optics ophthalmoscopy with calcium imaging to optically record optogenetically restored retinal ganglion cell activity in the fovea of the living primate. Recording from the intact eye of a living animal, we compare the patterns of activity evoked by the optogenetic actuator ChrimsonR with natural photoreceptor mediated stimulation in the same retinal ganglion cells. Optogenetic responses are recorded more than one year following administration of the therapy and two weeks after acute loss of photoreceptor input in the living animal. This in vivo imaging approach could be paired with any therapy to minimize the number of primates required to evaluate restored activity on the retinal level, while maximizing translational benefit by using an appropriate pre-clinical model of the human visual system. Nature Publishing Group UK 2020-04-03 /pmc/articles/PMC7125151/ /pubmed/32245977 http://dx.doi.org/10.1038/s41467-020-15317-6 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article McGregor, Juliette E. Godat, Tyler Dhakal, Kamal R. Parkins, Keith Strazzeri, Jennifer M. Bateman, Brittany A. Fischer, William S. Williams, David R. Merigan, William H. Optogenetic restoration of retinal ganglion cell activity in the living primate |
title | Optogenetic restoration of retinal ganglion cell activity in the living primate |
title_full | Optogenetic restoration of retinal ganglion cell activity in the living primate |
title_fullStr | Optogenetic restoration of retinal ganglion cell activity in the living primate |
title_full_unstemmed | Optogenetic restoration of retinal ganglion cell activity in the living primate |
title_short | Optogenetic restoration of retinal ganglion cell activity in the living primate |
title_sort | optogenetic restoration of retinal ganglion cell activity in the living primate |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7125151/ https://www.ncbi.nlm.nih.gov/pubmed/32245977 http://dx.doi.org/10.1038/s41467-020-15317-6 |
work_keys_str_mv | AT mcgregorjuliettee optogeneticrestorationofretinalganglioncellactivityinthelivingprimate AT godattyler optogeneticrestorationofretinalganglioncellactivityinthelivingprimate AT dhakalkamalr optogeneticrestorationofretinalganglioncellactivityinthelivingprimate AT parkinskeith optogeneticrestorationofretinalganglioncellactivityinthelivingprimate AT strazzerijenniferm optogeneticrestorationofretinalganglioncellactivityinthelivingprimate AT batemanbrittanya optogeneticrestorationofretinalganglioncellactivityinthelivingprimate AT fischerwilliams optogeneticrestorationofretinalganglioncellactivityinthelivingprimate AT williamsdavidr optogeneticrestorationofretinalganglioncellactivityinthelivingprimate AT meriganwilliamh optogeneticrestorationofretinalganglioncellactivityinthelivingprimate |