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The optoretinogram reveals the primary steps of phototransduction in the living human eye
Photoreceptors initiate vision by converting photons to electrical activity. The onset of the phototransduction cascade is marked by the isomerization of photopigments upon light capture. We revealed that the onset of phototransduction is accompanied by a rapid (<5 ms), nanometer-scale electromec...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9222118/ https://www.ncbi.nlm.nih.gov/pubmed/32917686 http://dx.doi.org/10.1126/sciadv.abc1124 |
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author | Pandiyan, Vimal Prabhu Maloney-Bertelli, Aiden Kuchenbecker, James A. Boyle, Kevin C. Ling, Tong Chen, Zhijie Charles Park, B. Hyle Roorda, Austin Palanker, Daniel Sabesan, Ramkumar |
author_facet | Pandiyan, Vimal Prabhu Maloney-Bertelli, Aiden Kuchenbecker, James A. Boyle, Kevin C. Ling, Tong Chen, Zhijie Charles Park, B. Hyle Roorda, Austin Palanker, Daniel Sabesan, Ramkumar |
author_sort | Pandiyan, Vimal Prabhu |
collection | PubMed |
description | Photoreceptors initiate vision by converting photons to electrical activity. The onset of the phototransduction cascade is marked by the isomerization of photopigments upon light capture. We revealed that the onset of phototransduction is accompanied by a rapid (<5 ms), nanometer-scale electromechanical deformation in individual human cone photoreceptors. Characterizing this biophysical phenomenon associated with phototransduction in vivo was enabled by high-speed phase-resolved optical coherence tomography in a line-field configuration that allowed sufficient spatiotemporal resolution to visualize the nanometer/millisecond-scale light-induced shape change in photoreceptors. The deformation was explained as the optical manifestation of electrical activity, caused due to rapid charge displacement following isomerization, resulting in changes of electrical potential and surface tension within the photoreceptor disc membranes. These all-optical recordings of light-induced activity in the human retina constitute an optoretinogram and hold remarkable potential to reveal the biophysical correlates of neural activity in health and disease. |
format | Online Article Text |
id | pubmed-9222118 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-92221182022-07-01 The optoretinogram reveals the primary steps of phototransduction in the living human eye Pandiyan, Vimal Prabhu Maloney-Bertelli, Aiden Kuchenbecker, James A. Boyle, Kevin C. Ling, Tong Chen, Zhijie Charles Park, B. Hyle Roorda, Austin Palanker, Daniel Sabesan, Ramkumar Sci Adv Research Articles Photoreceptors initiate vision by converting photons to electrical activity. The onset of the phototransduction cascade is marked by the isomerization of photopigments upon light capture. We revealed that the onset of phototransduction is accompanied by a rapid (<5 ms), nanometer-scale electromechanical deformation in individual human cone photoreceptors. Characterizing this biophysical phenomenon associated with phototransduction in vivo was enabled by high-speed phase-resolved optical coherence tomography in a line-field configuration that allowed sufficient spatiotemporal resolution to visualize the nanometer/millisecond-scale light-induced shape change in photoreceptors. The deformation was explained as the optical manifestation of electrical activity, caused due to rapid charge displacement following isomerization, resulting in changes of electrical potential and surface tension within the photoreceptor disc membranes. These all-optical recordings of light-induced activity in the human retina constitute an optoretinogram and hold remarkable potential to reveal the biophysical correlates of neural activity in health and disease. American Association for the Advancement of Science 2020-09-09 /pmc/articles/PMC9222118/ /pubmed/32917686 http://dx.doi.org/10.1126/sciadv.abc1124 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Pandiyan, Vimal Prabhu Maloney-Bertelli, Aiden Kuchenbecker, James A. Boyle, Kevin C. Ling, Tong Chen, Zhijie Charles Park, B. Hyle Roorda, Austin Palanker, Daniel Sabesan, Ramkumar The optoretinogram reveals the primary steps of phototransduction in the living human eye |
title | The optoretinogram reveals the primary steps of phototransduction in the living human eye |
title_full | The optoretinogram reveals the primary steps of phototransduction in the living human eye |
title_fullStr | The optoretinogram reveals the primary steps of phototransduction in the living human eye |
title_full_unstemmed | The optoretinogram reveals the primary steps of phototransduction in the living human eye |
title_short | The optoretinogram reveals the primary steps of phototransduction in the living human eye |
title_sort | optoretinogram reveals the primary steps of phototransduction in the living human eye |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9222118/ https://www.ncbi.nlm.nih.gov/pubmed/32917686 http://dx.doi.org/10.1126/sciadv.abc1124 |
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