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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
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.
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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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